OA19221A - Highly concentrated low viscosity MASP-2 inhibitory antibody formulations, kits, and methods - Google Patents

Abstract

The present invention relates to stable, highconcentration low-viscosity formulations of MASP2 inhibitory antibodies, kits comprising the formulations and therapeutic methods using the formulations and kits for inhibiting the adverse effects of MASP-2 dependent complement activation.

Description

HIGHLY CONCENTRATED LOW VISCOSITY MASP-2 INHIBITORY ANTIBODY

FORMULATIONS, KITS, AND METHODS

CROSS-REFERENCE TO RELATED APPLICATIONS

This application daims the benefit of US Provisional Application No. 62/382,156, filed August 31, 2016, which is hereby incorporated by reference in its entirety.

FIELD OF THE INVENTION

The présent invention relates to stable, high-concentration low-viscosity formulations of MASP-2 inhibitory antibodies, kits comprising the formulations and therapeutic methods using the formulations and kits for inhibiting the adverse effects of MASP-2 dépendent complément activation.

STATEMENT REGARD ING SEQUENCE LISTING

The sequence listing associated with this application is provided in text format in lieu of a paper copy and is hereby incorporated by reference into the spécification. The name of the text file containing the sequence listing is MP_l_0261_PCT_SequenceListing_20170809_ST25. The text file is 17 KB; was created on August 9, 2017; and is being submitted via EFS-Web with the filing of the spécification.

BACKGROUND

Antibody-based therapy is usually administered on a regular basis and often requires several mg/kg dosing by injection. A preferred form of delivery for treating chronic conditions is outpatient administration of high-dose monoclonal antibodies (several mg per kg) via subcutaneous (SC) injection (Stockwin and Holmes, Expert Opin Biol Ther 3:11331152 (2003); Shire et al., J Pharm Sci 93:1390-1402 (2004)). Highly concentrated pharmaceutical formulations of a therapeutic antibody are désirable because they allow lower volume administration and/or fewer administrations which consequently mean less discomfort to the patient. Additionally, such lower volumes allow packaging of the therapeutic doses of a monoclonal antibody in individual single-dose, pre-filled syringes for self-administration. SC delivery via pre-filled syringe or auto-injector technology allows for home administration and improved patient compliance of drug administration.

However, the development of a formulation with a high protein concentration poses challenges related to the physical and chemical stability of the protein, as well as difficulty with manufacture, storage and delivery of the protein formulation (see e.g., Wang et al., J of

Pharm Sci vol 96(1):1-26, (2007)). A challenge in the development of high protein concentration formulations is concentration-dependent solution viscosity. At a given protein concentration, viscosity varies dramatically as a function of the formulation. In particular, monoclonal antibodies are known to exhibit peculiar and diverse viscosity-concentration profiles that reveal a sharp exponential increase in solution viscosity with increasing monoclonal antibody concentration (see e.g., Connolly B.D. et al., Biophysical Journal vol 103:69-78, (2012)). Another challenge with liquid formulations at high monoclonal antibody concentration is protein physical stability (Alford et al., J. Pharm Sci 97:3005-3021 (2008); Salinas et al., J Pharm Sci 99:82-93 (2010); Sukumar et al., Pharm Res 21:1087-1093 (2004)). Therefore, the high viscosity of monoclonal antibody pharmaceutical formulations at high concentrations together with the potential for decreased stability can impede their development as products suitable for subcutaneous and/or intravenous delivery.

The complément System plays a rôle in the inflammatory response and becomes activated as a resuit of tissue damage or microbial infection. Complément activation must be tightly regulated to ensure sélective targeting of invading microorganisms and avoid selfinflicted damage (Ricklin et al., Nat. Immunol. 11:785-797, 2010). Currently, it is widely accepted that the complément System can be activated through three distinct pathways: the classical pathway, the lectin pathway, and the alternative pathway. The classical pathway is usually triggered by a complex composed of host antibodies bound to a foreign particle (z.e., an antigen) and generally requires prior exposure to an antigen for the génération of a spécifie antibody response. Since activation of the classical pathway dépends on a prior adaptive immune response by the host, the classical pathway is part of the acquired immune System. In contrast, both the lectin and alternative pathways are independent of adaptive immunity and are part of the innate immune System.

Mannan-binding lectin-associated serine protease-2 (MASP-2) has been shown to be required for the function of the lectin pathway, one of the principal complément activation pathways (Vorup-Jensen et aL, J. Immunol 165:2093-2100, 2000; Ambrus et al., JImmunol. 170:1374-1382, 2003; Schwaeble et al., PNAS 108:7523-7528, 2011). Importantly, inhibition of MASP-2 does not appear to interfère with the antibody-dependent classical complément activation pathway, which is a critical component of the acquired immune response to infection. As described in U.S. Patent No. 9,011,860 (assigned to Omeros corporation), which is hereby incorporated by reference, OMS646, a fully human monoclonal antibody targeting human MASP-2 has been generated which binds to human MASP-2 with high affinity and blocks the lectin pathway complément activity and is therefore useful to treat various lectin complément pathway-associated diseases and disorders.

As further described in U.S. Patent No. 7,919,094, U.S. Patent No. 8,840,893, U.S. Patent No.8,652,477, U.S. Patent No. 8,951,522, U.S. Patent No. 9,011,860; U.S. Patent No. 9,644,035, U.S. Patent Application Publication Nos. US2013/0344073, US2013/0266560, US 2015/0166675; US2017/0189525; and co-pending U.S. Patent Application Serial Nos. 15/476,154, 15/347,434, 15/470,647, 62/315,857, 62/275,025 and 62/527,926 (each of which is assigned to Omeros Corporation, the assignée of the instant application, each of which is hereby incorporated by reference), MASP-2-dependent complément activation has been implicated as contributing to the pathogenesis of numerous acute and chronic disease states. Therefore, a need exists for a stable, high-concentration, low-viscosity formulation of a MASP-2 monoclonal antibody that is suitable for parentéral (e.g., subcutaneous) administration, for treatment of subject suffering from MASP-2 complément pathwayassociated diseases and disorders.

SUMMARY

In one aspect, the présent disclosure provides a stable pharmaceutical formulation suitable for parentéral administration to a mammalian subject, comprising: (a) an aqueous solution comprising a buffer System having a pH of 5.0 to 7.0; and (b) a monoclonal antibody or fragment thereof that specifically binds to human MASP-2 at a concentration of about 50 mg/mL to about 250 mg/mL, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising CDR-H1, CDR-H2 and CDR-H3 of SEQ ID NO:2 and (ii) a light chain variable région comprising CDR-L1, CDR-L2 and CDR-L3 of SEQ ID NO:3, or a variant thereof comprising a heavy chain variable région having at least 95% identity to SEQ ID NO:2 and a light chain variable région having at least 95% identity to SEQ ID NO:3; wherein the formulation has a viscosity of between 2 and 50 centipoise (cP), and wherein the formulation is stable when stored at between 2°C and 8°C for at least one month. In some embodiments, the concentration of the antibody in the formulation is from about 150 mg/mL to about 200 mg/mL. In some embodiments, the viscosity of the formulation less than 25 cP. In some embodiments, the buffering System comprises histidine. In some embodiments, the buffering System comprises citrate. In some embodiments, the formulation further comprises an excipient, such as a tonicity modifying agent in a sufficient amount for the formulation to be hypertonie. In some embodiments, the formulation further comprises a surfactant. In some embodiments, the formulation further comprises a hyaluronidase enzyme in an amount effective to increase the dispersion and/or absorption of the antibody following subcutaneous administration.

In another aspect, the formulation is contained within a subcutaneous administration device, such as a pre-filled syringe.

In another aspect, the présent disclosure provides a kit comprising a pre-filled container containing the formulation.

In another aspect, the présent disclosure provides a pharmaceutical composition for use in treating a patient suffering from, or at risk for developing a MASP-2-dependent disease or condition, wherein the composition is a stérile, single-use dosage form comprising from about 350 mg to about 400 mg (i.e., 350 mg, 360 mg, 370 mg, 380 mg, 390 mg, or 400 mg) of MASP-2 inhibitory antibody, wherein the composition comprises about 1.8 mL to about 2.2 mL (i.e., 1.8 mL, 1.9mL, 2.0 mL, 2.1 mL or 2.2 mL) of a 185 mg/mL antibody formulation, such as disclosed herein, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising the amino acid sequence set forth in SEQ ID NO:2 and (ii) a light chain variable région comprising the amino acid sequence set forth in SEQ ID NO:3; and wherein the formulation is stable when stored at between 2°C and 8°C for at least six months. In some embodiments, the MASP-2 dépendent disease or condition is selected from the group consisting of aHUS, HSCT-TMA, IgAN and Lupus Nephritis (LN).

In another aspect, the présent disclosure provides a method of treating a subject suffering from a disease or disorder amenable to treatment with a MASP-2 inhibitory antibody comprising administering the formulation comprising a MASP-2 antibody, as disclosed herein.

DESCRIPTION OF THE DRAWINGS

The foregoing aspects and many of the attendant advantages of this invention will become more readily appreciated as the same become better understood by reference to the following detailed description, when taken in conjunction with the accompanying drawings, wherein:

FIGURE IA graphically illustrâtes the amount of lectin pathway-dependent membrane attack complex (MAC) déposition in the presence of different amounts of human MASP-2 monoclonal antibody (OMS646), demonstrating that OMS646 inhibits lectin mediated MAC déposition with an IC50 value of approximately 1 nM, as described in Example 1;

FIGURE IB graphically illustrâtes the amount of classical pathway-dependent MAC déposition in the presence of different amounts of human MASP-2 monoclonal antibody (OMS646), demonstrating that OMS646 does not inhibit classical pathway-mediated MAC déposition, as described in Example 1 ;

FIGURE IC graphically illustrâtes the amount of alternative pathway-dependent MAC déposition in the presence of human MASP-2 monoclonal antibody (OMS646), demonstrating that OMS646 does not inhibit alternative pathway-mediated MAC déposition, as described in Example 1 ;

FIGURE 2A graphically illustrâtes the results for Dynamic Light Scattering (DLS) analysis for OMS646 formulation excipient screening, showing the overall particle diameter observed for formulations containing various candidate excipients, as described in Example 2;

FIGURE 2B graphically illustrâtes the results for DLS analysis for OMS646 formulation excipient screening, showing the overall polydispersity observed for formulations containing various candidate excipients, as described in Example 2;

FIGURE 3 graphically illustrâtes the results of viscosity analysis of a range of OMS646 concentrations in various formulations as measured at pH 5.0 and pH 6.0, as described in Example 2;

FIGURE 4 graphically illustrâtes the percent protein recovery following bufferexchange for the OMS646 solubility/viscosity study with various candidate formulations, as described in Example 2;

FIGURE 5 graphically illustrâtes the viscosity (as determined by exponential fit of the viscosity data) versus protein concentration for the OMS646 solubility/viscosity study with various candidate formulations, as described in Example 2;

FIGURE 6 graphically illustrâtes the protein concentration-normalized viscosity data for the viscosity study with various candidate OMS646 formulations, as described in Example 2;

FIGURE 7A graphically illustrâtes the average load (Ibf) of three candidate OMS646 formulations in a syringeability study using 27 GA (1.25”), 25GA (1”) and 25GA thin-walled (1”) needles as described in Example 3; and

FIGURE 7B graphically illustrâtes the maximum load (Ibf) of three candidate OMS646 formulations in a syringeability study using 27 GA (1.25”), 25GA (1”) and 25GA thin-walled (1”) needles as described in Example 3.

DESCRIPTION OF THE SEQUENCE LISTING

SEQ ID NO:1 human MASP-2 protein (mature)

SEQ ID NO:2: OMS646 heavy chain variable région (VH) polypeptide

SEQ ID NO:3: OMS646 light chain variable région (VL) polypeptide

SEQ ID NO:4: OMS646 heavy chain IgG4 mutated heavy chain full length polypeptide SEQ ID NO:5: OMS646 light chain full length polypeptide

SEQ ID NO:6: DNA encoding OMS646 full length heavy chain polypeptide SEQ ID NO:7: DNA encoding OMS646 full length light chain polypeptide.

DETAILED DESCRIPTION

I. DEFINITIONS

Unless specifically defined herein, ail ternis used herein hâve the same meaning as would be understood by those of ordinary skill in the art of the présent invention. The following définitions are provided in order to provide clarity with respect to the terms as they are used in the spécification and daims to describe the présent invention.

Standard techniques may be used for recombinant DNA, oligonucleotide synthesis, and tissue culture and transformation (e.g., electroporation, lipofection). Enzymatic reactions and purification techniques may be performed according to manufacturer^ spécifications or as commonly accomplished in the art or as described herein. These and related techniques and procedures may be generally performed according to conventional methods well known in the art and as described in various general and more spécifie references that are cited and discussed throughout the présent spécification. See e.g., Sambrook et al., 2001, MOLECULAR CLONING: A LABORATORY MANUAL, 3d ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.; Current Protocols in Molecular Biology (Greene PubL Assoc. Inc. & John Wiley & Sons, Inc., NY, NY); Current Protocols in Immunology (Edited by: John E. Coligan, Ada M. Kruisbeek, David H. Margulies, Ethan M. Shevach, Warren Strober 2001 John Wiley & Sons, NY, NY); or other relevant Current Protocol publications and other like references. Unless spécifie définitions are provided, the nomenclature utilized in connection with, and the laboratory procedures and techniques of, molecular biology, analytical chemistry, synthetic organic chemistry, and médicinal and pharmaceutical chemistry described herein are those well known and commonly used in the art. Standard techniques may be used for recombinant technology, molecular biological, microbiological, chemical synthèses, chemical analyses, pharmaceutical préparation, formulation, and delivery, and treatment of patients.

The term “pharmaceutical formulation” refers to a préparation that is in such form as to permit the biological activity of the active agent (e.g., MASP-2 inhibitory antibody) to be effective for treatment, and which contains no additional components that are unacceptably toxic to a subject in which the formulation would be administered. Such formulations are stérile. In one embodiment, the pharmaceutical formulation is suitable for parentéral administration, such as subcutaneous administration.

The term “MASP-2” refers to mannan-binding lectin-associated serine protease-2. Human MASP-2 protein (mature) is set forth as SEQ ID NO:1.

The term MASP-2-dependent complément activation comprises MASP-2dependent activation of the lectin pathway, which occurs under physiological conditions (i.e., in the presence of Ca⁺⁺) leading to the formation of the lectin pathway C3 convertase C4b2a and upon accumulation of the C3 cleavage product C3b subsequently to the C5 convertase C4b2a(C3b)n.

The term lectin pathway refers to complément activation that occurs via the spécifie binding of sérum and non-serum carbohydrate-binding proteins including mannan-binding lectin (MBL), CL-11 and the ficolins (H-ficolin, M-ficolin, or L-ficolin).

The term classical pathway refers to complément activation that is triggered by an antibody bound to a foreign particle and requires binding of the récognition molécule Clq.

The term MASP-2 inhibitory antibody refers to an antibody, or antigen binding fragment thereof, that binds to MASP-2 and effectively inhibits MASP-2-dependent complément activation (e.g., OMS646). MASP-2 inhibitory antibodies useful in the method of the invention may reduce MASP-2-dependent complément activation by greater than 20%, such as greater than 30%, or greater than 40%, or greater than 50%, or greater than 60%, or greater than 70%, or greater than 80%, or greater than 90%, or greater than 95%.

The term OMS646 monoclonal antibody refers to a monoclonal antibody comprising CDR-H1, CDR-H2 and CDR-H3 of the heavy chain variable région amino acid sequence set forth in SEQ ID NO:2 and comprising CDR-L1, CDR-L2 and CDR-L3 of the light chain variable région amino acid sequence set forth in SEQ ID NO:3. This particular antibody is an example of a MASP-2 inhibitory antibody that specifïcally binds to MASP-2 and inhibits MASP-2 dépendent complément activation.

A “monoclonal antibody refers to a homogeneous antibody population wherein the monoclonal antibody is comprised of amino acids (naturally occurring and non-naturally occurring) that are involved in the sélective binding of an epitope. Monoclonal antibodies are highly spécifie for the target antigen. The term monoclonal antibody encompasses not only intact monoclonal antibodies and full-length monoclonal antibodies, but also fragments thereof (such as Fab, Fab', F(ab')2, Fv), single chain (scFv), variants thereof, fusion proteins comprising an antigen-binding portion, humanized monoclonal antibodies, chimeric monoclonal antibodies, and any other modified configuration of the immunoglobulin molécule that comprises an antigen-binding fragment (epitope récognition site) of the required specificity and the ability to bind to an epitope. It is not intended to be limited as regards the source of the antibody or the manner in which it is made (e.g., by hybridoma, phage sélection, recombinant expression, transgenic animais, etc.). The term includes whole immunoglobulins as well as the fragments etc. described above under the définition of antibody.

The term antibody fragment refers to a portion derived from or related to a full-length antibody, such as, for example, a MASP-2 inhibitory antibody, generally including the antigen binding or variable région thereof. Illustrative examples of antibody fragments include Fab, Fab', F(ab)2, F(ab')2 and Fv fragments, scFv fragments, diabodies, linear antibodies, single-chain antibody molécules and multispecific antibodies formed from antibody fragments.

As used herein, a single-chain Fv or scFv antibody fragment comprises the and Vl domains of an antibody, wherein these domains are présent in a single polypeptide chain. Generally, the Fv polypeptide further comprises a polypeptide linker between the and V_L domains, which enables the scFv to form the desired structure for antigen binding.

The term “CDR région” or “CDR” is intended to indicate the hypervariable régions of the heavy and light chains of the immunoglobulin as defined by Kabat et al., 1991 (Kabat, E. A. et al., (1991) Sequences of Proteins of Immunological Interest, 5^th Edition and later éditions. An antibody typically contains 3 heavy chain CDRs and 3 light chain CDRs. The term CDR or CDRs is used here in order to indicate, according to the case, one of these régions, or several, or even the whole, of these régions which contain the majority of the amino acid residues responsible for the binding by affinity of the antibody for the antigen of the epitope which it recognizes.

The term spécifie binding refers to the ability of an antibody to preferentially bind to a particular analyte that is présent in a homogeneous mixture of different analytes. In certain embodiments, a spécifie binding interaction will discriminate between désirable and undesirable analytes in a sample, in some embodiments more than about 10 to 100-fold or more (e.g., more than about 1000- or 10,000-fold). In certain embodiments, the affinity between a capture agent and analyte when they are specifically bound in a capture agent/analyte complex is characterized by a Kp> (dissociation constant) of less than about 100 nM, or less than about 50 nM, or less than about 25 nM, or less than about 10 nM, or less than about 5 nM, or less than about 1 nM.

The term isolated antibody refers to an antibody that has been identified and separated and/or recovered and/or purified from a component of its natural environment or cell culture expression System. In preferred embodiments, the antibody will be purified (1) to greater than 95% by weight of antibody and most preferably more than 99% by weight; as determined by a suitable method to measure protein concentration, such as, for example, the Lowry method, or absorbance at OD280, (2) to a degree sufficient to obtain at least 15 residues of N-terminal or internai amino acid sequence by use of a spinning cup sequenator; or (3) to homogeneity by SDS-PAGE under reducing or non-reducing conditions using Coomassie blue or, preferably, silver stain. Typically an isolated antibody for use in the formulations disclosed herein will be prepared by at least one purification step.

As used herein, the amino acid residues are abbreviated as follows: alanine (Ala;A), asparagine (Asn;N), aspartic acid (Asp;D), arginine (Arg;R), cysteine (Cys;C), glutamic acid (Glu;E), glutamine (Gln;Q), glycine (Gly;G), histidine (Hush), isoleucine (Ilia), leucine (Lull), lysine (Lys;K), méthionine (Met;M), phenylalanine (Phe;F), proline (Pro;P), serine (Ser;S), threonine (Thr;T), tryptophan (Trp;W), tyrosine (Tyr;Y), and valine (Val;V).

In the broadest sense, the naturally occurring amino acids can be divided into groups based upon the chemical characteristic of the side chain of the respective amino acids. By hydrophobie amino acid is meant either Ile, Leu, Met, Phe, Trp, Tyr, Val, Ala, Cys or Pro. By hydrophilic amino acid is meant either Gly, Asn, Gin, Ser, Thr, Asp, Glu, Lys, Arg or His. This grouping of amino acids can be further subclassed as follows. By uncharged hydrophilic amino acid is meant either Ser, Thr, Asn or Gin. By acidic amino acid is meant either Glu or Asp. By basic amino acid is meant either Lys, Arg or His.

As used herein the term conservative amino acid substitution is illustrated by a substitution among amino acids within each of the following groups: (1) glycine, alanine, valine, leucine, and isoleucine, (2) phenylalanine, tyrosine, and tryptophan, (3) serine and threonine, (4) aspartate and glutamate, (5) glutamine and asparagine, and (6) lysine, arginine and histidine.

As used herein, a subject includes ail mammals, including without limitation, humans, non-human primates, dogs, cats, horses, sheep, goats, cows, rabbits, pigs and rodents.

The term “pharmaceutical ly acceptable” with respect to an excipient in a pharmaceutical formulation means that the excipient is suitable for administration to a human subject.

The term “subcutaneous administration” refers to administration of a formulation under ail layers of the skin of a subject.

The term buffer refers to a buffered solution that resists changes in pH by the action of its acid-base conjugate components. The buffer of this invention has a pH in the range from about 4 to about 8; preferably from about 5 to about 7; and most preferably has a pH in the range from about 5.5 to about 6.5. Examples of buffers that will control the pH in this range include acetate (e.g., sodium acetate), succinate (such as sodium succinate), gluconate, histidine, citrate, and other organic acid buffers. A “buffering agent” is a compound that is used to produce buffered solutions.

The term “histidine” specifically includes L-histidine unless otherwise specified.

The term isotonie refers to a formulation that has essentially the same osmotic pressure as human blood. Isotonie formulations will generally hâve an osmotic pressure from about 250 to about 350 mOsmol/KglHbO. Isotonicity can be measured using a vapor pressure or freezing point dépréssion osmometer, for example.

The term “hypertonie” refers to a formulation with an osmotic pressure above that of human (i.e., greater than 350 mOsm/KgtEO).

The term “tonicity modifying agent” refers to a pharmaceutically acceptable agent suitable to provide an isotonie, or in some embodiments, a hypertonie formulation.

The term “stérile” refers to a pharmaceutical product that is asceptic or free of viable bacteria, fungi or other microorganisms, which can be achieved by any suitable means, such as, for example, a formulation that has been aseptically processed and filled, or filtered through stérile filtration membranes, prior to, or following, préparation of the formulation and filled.

The terni “stable formulation” refers to maintenance of the starting level of purity of a formulation over a period of time. In other words, if a formulation is at least 95% pure, such as at least 96% pure, at least 97% pure, at least 98% pure or at least 99% pure with respect to a given antibody species (e.g., MASP-2 inhibitory antibody) at time 0, stability is a measure of how well and for how long the formulation retains substantially this level of purity (e.g., without formation of other species, such as fragmented portions (LMW) or aggregates of the pure species (HMW)). A formulation is stable if the level of purity does not decrease substantially when stored at approximately 2-8°C over a given period of time, such as at least 6 months, at least 9 months, at least 12 months, or at least 24 months. By “not decrease substantially,” is meant that the level of purity of the formulation changes by less than 5%, such as by less than 4%, or by less than 3%, or by less than 2% or by less than 1% per time period (e.g., over 6 months, over 9 months or over 12 months or over 24 months). In one embodiment, a stable formulation is stable at a température of from 2-8°C for a period of at least six months. In a preferred embodiment, a stable formulation is stable at a température of from 2-8°C for a period of at least one year, or for a period of at least two years. In one embodiment, the formulation is stable if the MASP-2 inhibitory antibody remains at least 95% monomeric during storage at 2°C to 8°C for at least one month, or for at least six months, or for at least 12 months, as determined by SEC-HPLC.

The term preservative refers to a compound which can be included in a formulation to essentially reduce bacterial growth or contamination. Non-Iimiting examples of potential preservatives include octadecyldimethylbenzyl ammonium chloride, hexaméthonium chloride, benzalkonium chloride (a mixture of alkylbenzyldimethylammonium chlorides in which the alkyl groups are long-chain compounds), and benzéthonium chloride. Other types of preservatives include aromatic alcohols such as phénol, butyl and benzyl alcohol, alkyl parabens such as methyl or propyl paraben, catechol, resorcinol, cyclohexanol, 3-pentanol, and m-cresol.

The term “excipient” refers to an inert substance in a formulation which imparts a bénéficiai physical property to a formulation such as increased protein stability and/or decreased viscosity. Examples of suitable excipients include, but are not limited to, proteins (e.g., sérum albumin), amino acids (e.g., aspartic acid, glutamic acid, lysine arginine, glycine and histidine), saccharides (e.g., glucose, sucrose, maltose and trehalose), polyols (e.g., mannitol and sorbitol), fatty acids and phospholipids (e.g., alkyl sulfonates and caprylate).

The term substantially free means that either no substance is présent or only minimal, trace amounts of the substance are présent which do not hâve any substantial impact on the properties of the composition. If reference is made to no amount of a substance, it should be understood as no détectable amount.”

The term “viscosity” refers to the measure of the résistance of a fluid which is being deformed by either shear stress or tensile stress; it can be evaluated using a viscometer (e.g., a rolling bail viscometer) or rheometer. Unless otherwise indicated, the viscosity measurement (centipoise, cP) is that at about 25°C with a shear rate in the range of 100,000 to 250,000 1/sec.

The term “parentéral administration” refers to a route of administration other than by way of the intestines and includes injection of a dosage form into the body by a syringe or other mechanical device such as an infusion pump. Parentéral routes can include intravenous, intramuscular, subcutaneous and intraperitoneal routes of administration. Subcutaneous injection is a preferred route of administration.

The term treatment refers to therapeutic treatment and/or prophylactic or preventative measures. Those in need of treatment include the subjects already having the disease as well as those in which the disease is to be prevented. Hence, the patient to be treated herein may hâve been diagnosed as having the disease or may be predisposed or susceptible to the disease.

The term effective amount refers to an amount of a substance that provides the desired effect. In the case of a pharmaceutical drug substance it is the amount of active ingrédient effective to treat a disease in the patient. In the case of a formulation ingrédient, for example, a hyaluronidase enzyme, an effective amount is the amount necessary to increase the dispersion and absorption of the co-administered MASP-2 inhibitory antibody in such a way that the MASP-2 inhibitory antibody can act in a therapeutically effective way as outlined above.

As used herein, the term “about” as used herein is meant to specify that the spécifie value provided may vary to a certain extent, such as a variation in the range of ±10%, preferably ±5%, most preferably ±2% are included in the given value. For example, the phrase “a pharmaceutical formulation having about 200 mg/tnL MASP-2 inhibitory antibody” is understood to mean that the formulation can hâve from 180 mg/mL to 220 mg/mL MASP-2 inhibitory antibody (e.g., OMS646). Where ranges are stated, the endpoints are included within the range unless otherwise stated or otherwise évident from the context.

As used herein the singular forms a, an and the include plural aspects unless the context clearly dictâtes otherwise. Thus, for example, reference to an excipient includes a plurality of such excipients and équivalents thereof known to those skilled in the art, reference to an agent includes one agent, as well as two or more agents; reference to an antibody includes a plurality of such antibodies and reference to a framework région includes reference to one or more framework régions and équivalents thereof known to those skilled in the art, and so forth.

Each embodiment in this spécification is to be applied mutatis mutandis to every other embodiment unless expressly stated otherwise. It is contemplated that any embodiment discussed in this spécification can be implemented with respect to any method, kit, reagent, or composition of the invention, and vice versa. Furthermore, compositions of the invention can be used to achieve methods of the invention.

II. Overview of the Invention

The présent disclosure provides stable, high-concentration low-viscosity MASP-2 inhibitory antibody pharmaceutical formulations suitable for parentéral administration (e.g., subcutaneous administration) and also suitable for dilution prior to intravenous administration. Highly concentrated pharmaceutical formulations of therapeutic antibody are désirable because they allow lower volume administration and/or fewer administrations, which consequently mean less discomfort to the patient. Additionally, such lower volumes allow packaging of the therapeutic doses of MASP-2 inhibitory antibody in individual singledose, pre-filled syringes or vials for self-administration. The high-concentration, lowviscosity formulations of the présent disclosure comprise an aqueous solution comprising a buffer System having a pH of 4.0 to 8.0, more preferably having a pH of about 5.0 to about 7.0, and a MASP-2 inhibitory monoclonal antibody (e.g., OMS646) or antigen-binding fragment thereof at a concentration of about 50 mg/mL to about 250 mg/mL. In preferred embodiments, the MASP-2 inhibitory antibody (e.g., OMS646) is présent in the high concentration formulations suitable for subcutaneous administration at a concentration of from about 100 mg/mL to about 250 mg/mL. In particular embodiments, the MASP-2 inhibitory antibody (e.g., OMS646) is présent in the high concentration formulations at a concentration of from about 150 mg/mL to about 200 mg/mL, such as about 175 mg/mL to about 195 mg/mL, such as about 185 mg/mL.

In various embodiments, the pharmaceutical formulations further comprise, in addition to the highly concentration MASP-2 inhibitory antibody and buffer System, one or more excipients, such as a tonicity modifying agent (e.g., an amino acid with a charged side chain), and optionally a non-ionic surfactant. In some embodiments, the pharmaceutical formulations in accordance with this disclosure further comprise a hyaluronidase enzyme.

A significant advantage of the highly concentrated pharmaceutical formulations of MASP-2 inhibitory antibody of the présent invention is their low viscosity at high protein concentrations. As known to those skilled in the art, high viscosity of monoclonal antibody pharmaceutical formulations at concentrations >100 mg/mL can impede their development as products suitable for subcutaneous and/or intravenous delivery. Therefore, pharmaceutical formulations having lower viscosity are highly désirable because of their ease of manufacturability, such as but not limited to processing, filtering, and filling. As described in Examples 2 and 3 herein, the formulations of the présent disclosure comprising from 100 mg/mL to 200 mg/mL MASP-2 inhibitory antibody OMS646 hâve surprisingly low viscosity, such as a viscosity less than about 50 cP, such as between 2 cP and 50 cP, such as between 2 cP and 40 cP, such as between 2 cP and 30 cP, or between 2 cP and 25 cP, or between 2 cP and 20 cP, or between 2 cP and 18 cP.

Additionally, the low viscosity, highly concentrated MASP-2 inhibitory antibody pharmaceutical formulations of the présent invention allow the pharmaceutical formulations to be administered via standard syringe and needles, auto-injector devices, and microinfusion devices known in the art. As described in Example 3, the high concentration low viscosity of the MASP-2 inhibitory antibody pharmaceutical formulations as disclosed herein were determined to hâve syringeability and injectability suitable for subcutaneous administration. Syringeability and injectability are key product performance parameters of a pharmaceutical formulation intended for any parentéral administration, e.g., intramuscular or subcutaneous and permit the administration of such formulations by intramuscular or subcutaneous injection via small-bore needles typically used for such injections, such as, for example, 29GA regular or thin-walled, 27GA (1.25”) regular or thin-walled, or 25GA (1”) regular or thin-walled needles. In some instances, the low viscosity of MASP-2 inhibitory antibody pharmaceutical formulations as disclosed herein permit the administration of an acceptable (for example, 1-3 cc) injected volume while delivering an effective amount of the MASP-2 inhibitory antibody OMS646 in a single injection at a single injection site.

A further significant advantage of the formulations of the présent disclosure is that the high concentration low viscosity formulations of MASP-2 inhibitory antibody (i.e., >100 mg/mL to 200 mg/mL) are stable when stored at 2°C to 8° C for at least 30 days, up to at least 9 months, or up to at least 12 months or longer, as described in the stability studies in Examples 2 and 4.

The présent disclosure also provides a process for the préparation of the high concentration low viscosity MASP-2 inhibitory antibody formulations, containers including said formulations, therapeutic kits comprising the formulations; and to therapeutic methods of using such formulation, containers and kits for the treatment of a subject suffering from, or at risk for developing a disease or condition associated with MASP-2-dependent complément activation.

MASP-2 Inhibitory Antibody

As detailed herein, the présent invention is drawn to formulations comprising monoclonal antibodies that specifically bind to MASP-2 and inhibit MASP-2-dependent complément activation and antigen-binding fragments thereof. In certain embodiments, a MASP-2 inhibitory antibody or antigen-binding fragment thereof for use in the claimed formulations is a MASP-2 inhibitory antibody referred to as “OMS646” as described in WO2012/151481 (hereby incorporated herein by reference) which comprises a heavy chain polypeptide comprising the amino acid sequence of SEQ ID NO:2 and a light chain polypeptide comprising the amino acid sequence of SEQ ID NO:3. As described in WO2012/151481 and described in Example 1, OMS646 specifically binds to human MASP-2 with high affinity and has the ability to block lectin pathway complément activity. In certain embodiments, a MASP-2 inhibitory antibody or antigen-binding fragment thereof for use in the claimed formulations is a MASP-2 inhibitory antibody comprising a heavy-chain variable région comprising (i) CDR-H1 comprising the amino acid sequence from 31-35 of SEQ ID NO:2, (ii) CDR-H2 comprising the amino acid sequence from 50-65 of SEQ ID NO:2, and iii) CDR-H3 comprising the amino acid sequence from 95-107 of SEQ ID NO:2; and (b) a light-chain variable région comprising: i) CDR-L1 comprising the amino acid sequence from 24-34 of SEQ ID NO:3, ii) CDR-L2 comprising the amino acid sequence from 50-56 of SEQ ID NO:3, and iii) CDR-L3 comprising the amino acid sequence from 89-97 of SEQ ID NO:3. In some embodiments, the MASP-2 inhibitory antibody for use in the claimed formulations comprises a variant of OMS646 comprising a heavy chain variable région having at least 95% identity to SEQ ID NO:2 and comprising a light chain variable région having at least 95% identity to SEQ ID NO:3. In some embodiments, the MASP-2 inhibitory antibody for use in the claimed formulations comprises a variant of OMS646 comprising an amino acid sequence having at least 95% identity to SEQ ID NO:2, wherein residue 31 is an R, residue 32 is a G, residue 33 is a K, residue 34 is an M, residue 35 is a G, residue 36 is a V, residue 37 is an S, residue 50 is an L, residue 51 is an A, residue 52 is an H, residue 53 is an I, residue 54 is an F, residue 55 is an S, residue 56 is an S, residue 57 is a D, residue 58 is an E, residue 59 is a K, residue 60 is an S, residue 61 is a Y, residue 62 is an R, residue 63 is a T, residue 64 is an S, residue 65 is an L, residue 66 is a K, residue 67 is an S, residue 95 is a Y, residue 96 is a Y, residue 97 is a C, residue 98 is an A, residue 99 is an R, residue 100 is an I, residue 101 is an R, residue 102 is an R or A, residue 103 is a G, residue 104 is a G, residue 105 is an I, residue 106 is a D and residue 107 is a Y; and b) a light chain variable région comprising an amino acid sequence having at least 95% identity to SEQ ID NO:3, wherein residue 23 is an S, residue 24 is a G, residue 25 is an E or D, residue 26 is a K, residue 27 is an L, residue 28 is a G, residue 29 is a D, residue 30 is a K, residue 31 is a Y or F, residue 32 is an A, residue 33 is a Y, residue 49 is a Q, residue 50 is a D, residue 51 is a K or N, residue 52 is a Q or K, residue 53 is an R, residue 54 is a P, residue 55 is an S, residue 56 is a G, residue 88 is a Q, residue 89 is an A, residue 90 is a W, residue 91 is a D, residue 92 is an S, residue 93 is an S, residue 94 is a T, residue 95 is an A, residue 96 is a V and residue 97 is an F.

In some embodiments, the monoclonal MASP-2 inhibitory antibody (e.g., OMS646 or a variant thereof) for use in the claimed formulations is a full length monoclonal antibody. In some embodiments, the monoclonal MASP-2 inhibitory antibody is a human IgG4 full length antibody. In some embodiments, the IgG4 comprises a point mutation in the hinge région to enhance the stability of the antibody.

In some embodiments, the MASP-2 inhibitory antibody (e.g., OMS646 or a variant thereof) is comprised of variable régions of human origin fused to human IgG4 heavy chain and lambda light chain constant régions, wherein the heavy chain comprises a point mutation in the hinge région (e.g., wherein the IgG4 molécule comprises a S228P mutation) to enhance the stability of the antibody. In some embodiments, the MASP-2 inhibitory antibody is a tetramer consisting of two identical heavy chains having the amino acid sequence set forth in SEQ ID NO:4 and two identical light chains having the amino acid sequence set forth in SEQ IDNO:5.

In some embodiments, the concentration of the MASP-2 inhibitory antibody in the formulation is from about 100 mg/mL to about 250 mg/mL, such as about 150 mg/ml to about 220 mg/mL, such as about 175 mg/mL to about 200 mg/mL, or about 175 mg/mL to about 195 mg/mL. In certain embodiments, the MASP-2 inhibitory antibody is présent in the formulation at a concentration of about 175 mg/ml to about 195 mg/ml, such as about 180 mg/mL to about 190 mg/mL, such as about 175 mg/mL, such as about 180 mg/mL, about 181 mg/mL, about 182 mg/mL, about 183 mg/mL, about 184 mg/mL, about 185 mg/mL, about

186 mg/mL, about 187 mg/mL, about 188 mg/mL, about 189 mg/mL or such as about 190 mg/mL.

In some embodiments, minor variations in the amino acid sequences of the MASP-2 inhibitory antibodies or fragments thereof are contemplated as being encompassed by the claimed formulations, provided that the variations in the amino acid sequence maintains at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to the MASP-2 inhibitory antibodies or antigen-binding fragments thereof described herein (i.e., at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to SEQ ID NO:2 and/or at least at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to SEQ ID NO:3) and retain the ability to inhibit MASP-2-dependent complément activation.

As will be appreciated, MASP-2 inhibitory antibodies or antigen-binding fragments thereof that are formulated in the context of the présent disclosure can be produced using techniques well known in the art (e.g., recombinant technologies, phage display technologies, synthetic technologies, or combinations of such technologies or other technologies readily known in the art). Methods for producing and purifying antibodies and antigen-binding fragments are well known in the art and can be found, for example, in Harlow and Lane (1988) Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, Chapters 5-8 and 15.

For example, MASP-2 inhibitory antibodies, such as OMS646 can be expressed in a suitable mammalian cell line. Sequences encoding the heavy chain variable région and the light chain variable région of a particular antibody of interest such as OMS646 (e.g., SEQ ID NO:6 and SEQ ID NO:7) can be used to transform a suitable mammalian host cell. Methods for introducing heterologous polynucleotides into mammalian cells are well known in the art and include dextran-mediated transfection, calcium phosphate précipitation, polybrene mediated transfection, protoplast fusion, electroporation, encapsulation of the polynucleotide(s) in liposomes, and direct microinjection of the DNA into nuclei.

Mammalian cell lines available as hosts for expression are well known in the art and include many immortalized cell lines available from the American Type Culture Collection (ATCC), including but not limited to Chinese hamster ovary (CHO) cells, HeLa cells, baby hamster kidney (BNK) cells, monkey kidney cells (COS), human hepatocellular carcinoma cells (e.g., HepG2), human épithélial kidney 293 cells (HEK293) and numerous other cell lines.

Following the protein production phase of the cell culture process, MASP-2 inhibitory antibodies are recovered from the cell culture medium using techniques understood by one skilled in the art. In particular, in some embodiments the MASP-2 inhibitory antibody heavy and light chain polypeptides are recovered from the culture medium as secreted polypeptides.

MASP-2 inhibitory antibodies can be purified using, for example, hydroxyapatite chromatography, gel electrophoresis, dialysis, and affinity chromatography, and any combination of known or yet to be discovered purification techniques, including but not limited to Protein A chromatography, fractionation on an ion-exchange column, éthanol précipitation, reverse phase HPLC, chromatography on silica, chromatography on heparin SEPHAROSET®, an anion or cation exchange resin chromatography (such as a polyaspartic acid column), chromatofocusing, SDS- PAGE, and ammonium sulfate précipitation. The purification method can further comprise additional steps that inactivate and/or remove viruses and/or retroviruses that might potentially be présent in the cell culture medium of mammalian cell lines. A significant number of viral clearance steps are available, including but not limited to, treating with chaotropes such as urea or guanidine, détergents, additional ultrafiltration/diafiltration steps, conventional séparation, such as ion-exchange or size exclusion chromatography, pH extremes, heat, proteases, organic solvents or any combination thereof.

The purified MASP-2 inhibitory antibodies typically require concentration and a buffer exchange prior to storage or further processing. As a non-limiting example, a tangential flow filtration (TFF) System may be used to concentrate and exchange the elution buffer from the previous purification column with the final buffer desired for the drug substance.

The monoclonal MASP-2 inhibitory antibody which is formulated herein is preferably essentially pure and desirably essentially homogeneous (i.e., free from contaminating proteins, etc.). “Essentially pure” antibody means a composition comprising at least 90% by weight of the antibody, based on the total weight of the composition, preferably at least 95% by weight. “Essentially homogenous” antibody means a composition comprising at least about 99% by weight of antibody, based on total weight of the composition.

Aqueous Solutions

The high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure comprises an aqueous solution comprising a buffer System having a pH of 4.0 to 8.0 (e.g., having a pH from about 5.0 to about 7.0, or having a pH from about 5.5 to about 6.5) and a MASP-2 inhibitory antibody (e.g., OMS646 or a variant thereof) or antigenbinding fragment thereof at a concentration of about 50 mg/mL to about 250 mg/mL (e.g., from about lOOmg/mL to about 250 mg/mL). The aqueous solution for use in the formulations of the présent disclosure is one which is pharmaceutically acceptable (safe and non-toxic for administration to a human) and is useful for the préparation of a liquid formulation. In some embodiments, the aqueous solution is water, such as stérile water for injection (WFI), which is a stérile, solute-free préparation of distilled water. Alternatively, other aqueous solutions that are suitable for therapeutic administration and which would not adversely affect the stability of the formulation may be used, such as deionized water. Other suitable aqueous solutions include bacteriostatic water for injection (BWFI), stérile saline solution, Ringer’s solution, or other similar aqueous solutions used for pharmaceutical solutions.

Buffering Systems

The high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure is adjusted to a pH from 4.0 to 8.0, preferably from pH 5.0 to 7.0. The desired pH is suitably maintained by use of a buffering System. In some embodiments, the buffer System comprises at least one pharmaceutically acceptable buffering agent with an acid dissociation constant within 2 pH units of the formulation pH. The buffer System used in the formulations in accordance with the présent invention has a pH in the range from about 4.0 to about 8.0. Various buffering agents are known to the person skilled in the art. Examples of buffering agents that will control the pH in this range include acetate, succinate, gluconate, histidine, citrate, and other organic acid buffers. In some embodiments, the buffering agent is selected from the group consisting of succinate, histidine and citrate. In some embodiments, the pharmaceutical formulations comprise a buffering System with a buffering agent in a concentration of from 1 to 50 mM, such as from 10 to 40 mM, or such as from 10 to 30 mM, or from 20 to 30mM, or about 20 mM.

In some embodiments, the buffering agent is a histidine buffer. A “histidine buffer” is a buffer comprising the amino acid histidine. Examples of histidine buffers include histidine or any histidine salts including histidine hydrochloride, histidine acetate, histidine phosphate, and histidine sulfate, including combinations of any of these salts with or without histidine. In one embodiment, the buffering System comprises histidine hydrochloride buffer (LHistidine/HCL). Such histidine hydrochloride buffer may be prepared by titrating L-histidine (free base, solid) with diluted hydrochloric acid or by using the appropriate mixture of histidine and histidine hydrochloride. In some embodiments, the pH of the L-Histidine/HCl buffer is about 5.0 to about 7.0, such as about 5.5 to about 6.0, e.g., about 5.8 or about 5.9.

In some embodiments, the buffering agent is a citrate buffer. Such citrate buffer may be prepared by titrating citric acid, the mono-sodium sait of citric acid, and/or the di-sodium sait of citric acid with diluted sodium hydroxide solution to the appropriate pH or by using the appropriate mixture of citric acid and the salt(s) to achieve this same pH. In another embodiment, the citrate buffer may be prepared by titrating a tri-sodium citrate solution with diluted hydrochloric acid solution to the appropriate pH. In this case, the ionic strength may be slightly higher than starting with citric acid due to the génération of additional ions of sodium and chloride in the solution. In certain embodiments, the pH of the citrate buffer is about 5.0 to about 7.0, such as about 5.5 to about 6.0, e.g., about 5.8 or about 5.9. In some embodiments, the buffering agent is a succinate buffer. In certain embodiments, the pH of the succinate buffer is about 5.5 to about 6.0, e.g., about 5.8 or about 5.9.

In some embodiments, the buffering agent is a sodium citrate buffer, wherein sodium citrate is présent in the formulation at a concentration of about 10 mM to about 50 mM, such as from about 10 mM to about 25 mM, such as about 20 mM. In some embodiments, the buffering agent is a L-histidine buffer, wherein L-histidine is présent in the formulation at a concentration of about lOmM to about 50 mM, such as from about 10 mM to about 25 mM, such as about 20 mM. In some embodiments, the formulation comprises about 20 mM sodium citrate and has a pH from about 5.0 to about 7.0. In some embodiments, the formulation comprises about 20 mM L-histidine and has a pH from about 5.0 to about 7.0.

Excipients

In some embodiments, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure further comprises at least one excipient. Examples of suitable excipients include, but are not limited to, proteins (e.g., sérum albumin), amino acids (e.g., aspartic acid, glutamic acid, lysine, arginine, glycine and histidine), saccharides (e.g., glucose, sucrose, maltose and trehalose), polyols (e.g., mannitol and sorbitol), fatty acids and phospholipids (e.g., alkyl sulfonates and caprylate).

In some embodiments, the formulation comprises an excipient selected from the group consisting of an amino acid with a charged side chain, a sugar or other polyol and a sait. In some embodiments, the formulation comprises a sugar or other polyol, such as, for example, sucrose, trehalose, mannitol or sorbitol. In some embodiments, the formulation comprises a sait, such as, for example NaCI or a sait of an amino acid.

In some embodiments, the formulation comprises an excipient that is a tonicity modifying agent. In some embodiments, the tonicity modifying agent is included in the formulation in a concentration suitable to provide an isotonie formulation. In some embodiments, the tonicity modifying agent is included in the formulation in a concentration suitable to provide a hypertonie formulation. In some embodiments, the tonicity modifying agent for use in the formulation is selected from the group consisting of an amino acid with a charged side chain, a sugar or other polyol and a sait. In some embodiments, the tonicity modifying agent is an amino acid with a charged side chain (i.e., a negatively charged side chain or a positively charged side chain) at a concentration of from about 50 mM to about 300 mM. In some embodiments, the tonicity modifying agent is an amino acid with a negatively charged side chain, such as glutamate. In some embodiments, the formulation comprises glutamate at a concentration of about 50mM to about 300 mM. In some embodiments, the tonicity modifying agent is an amino acid with a positively charged side chain, such as arginine. In some embodiments, the formulation comprises arginine (e.g., arginine HCL), at a concentration of from about 50 mM to about 300 mM, such as from about 150 mM to about 225 mM.

Preferably, the pharmaceutical formulations as disclosed herein are hypertonie (i.e., hâve a higher osmotic pressure than human blood). As described herein, it was unexpectedly observed that hypertonicity led to reduced sample viscosity, which was achieved, for example, with modest increases in arginine concentration. As described in Example 2, it was unexpectedly observed that low viscosities were achieved (e.g., less than 25 cP) with the citrate/arginine and the histidine/arginine high concentration MASP-2 inhibitory antibody formulations comprising an arginine concentration of 200 mM or greater in the absence of CaCh. Accordingly, in some embodiments, the formulation comprises arginine (e.g., arginine HCL) at a hypertonie level of from about 200 mM to about 300 mM.

As further described in Example 2, it was also observed that formulations which included divalent cations (CaCh or MgCh) had elevated high molecular weight material as compared to formulations that did not include CaCh or MgCh additives. Accordingly, in one embodiment, the high-concentration, low viscosity MASP-2 inhibitory antibody formulation of the présent disclosure is substantially free of a CaCh additive. In one embodiment, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure is substantially free of a MgCh additive.

As further described in Example 2, it was determined for the high concentration MASP-2 antibody formulations that the inclusion of sucrose was associated with elevated polydispersity in ail buffering Systems tested. Accordingly, in one embodiment, the high concentration low viscosity MASP-2 inhibitory antibody formulation of the présent disclosure is substantially free of sucrose.

As described in Example 2, it was also determined for the high concentration MASP2 antibody formulations that the inclusion of sorbitol was associated with elevated polydispersity in ail buffering Systems tested. Accordingly, in one embodiment, the high concentration low viscosity MASP-2 inhibitory antibody formulation of the présent disclosure is substantially free of sorbitol.

Surfactants

Optionally, in some embodiments, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure further comprises a pharmaceutically acceptable surfactant. Non-limiting examples of suitable pharmaceutically acceptable surfactants include polyoxyethylensorbitan fatty acid esters (e.g., Tween), polyethylene-polypropylene glycols, polyoxyethylene-stearates, polyoxyethylene alkyl ethers (e.g., polyoxyethylene monolauryl ether), alkylphenylpolyoxyethylene ethers (e.g., Triton-X), polyoxyethylene-polyoxypropylene copolymer (e.g., Poloxamer and Pluronic), and sodium dodecyl sulphate (SDS). In certain embodiments, the pharmaceutically acceptable surfactant is a polyoxyethylenesorbitan-fatty acid ester (polysorbate), such as polysorbate 20 (sold under the trademark Tween 20™) and polysorbate 80 (sold under the trademark Tween 80™). In some embodiments, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure comprises a non-ionic surfactant. The nonionic surfactant can be a polysorbate, (e.g., selected from the group of polysorbate 20, polysorbate 80, and polyethylene-polypropylene copolymer). In some embodiments, the concentration of the surfactant is about 0.001 to 0.1% (w/v), or 0.005% to 0.1% (w/v), or 0.01 to 0.1% (w/v), or 0.01 to 0.08% (w/v), or 0.025 to 0.075% (w/v), or more particularly about 0.01% (w/v), about 0.02% (w/v), about 0.04% (w/v), or about 0.06% (w/v), or about 0.08% (w/v), or about 0.10% (w/v). In some embodiments, the formulation comprises a non-ionic surfactant (e.g., polysorbate 80) at a concentration of from about 0.001 to 0.1% (w/v), or 0.005% to 0.1% (w/v), or 0.01 to 0.1% (w/v), or 0.01 to 0.08% (w/v), or 0.025 to 0.075% (w/v), or more particularly about 0.01% (w/v), about 0.02% (w/v), about 0.04% (w/v), or about 0.06% (w/v), or about 0.08% (w/v), or about 0.10% (w/v). As described in Example 2, it was unexpectedly observed that the inclusion of the non-ionic surfactant polysorbate 80 (PS-80) led to a further réduction in viscosity while also preserving protein recovery, thereby allowing for a high concentration of OMS646 antibody while maintaining a low viscosity suitable for use in an injection device, such as an autoinjector.

Stabilizers

Optionally, in some embodiments, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure further comprises a stabilizer. The stabilizer (used synonymously with the term stabilizing agent herein) may be a carbohydrate or saccharide or a sugar admitted by the regulatory authorities as a suitable additive or excipient in pharmaceutical formulations, e.g., trehalose or sucrose. The typical concentration of the stabilizer is 15 to 250 mM, or 150 to 250 mM, or about 210 mM. The formulations may contain a secondary stabilizer, such as méthionine, e.g., in a concentration of 5 to 25 mM or in a concentration of 5 to 15 mM (e.g., méthionine in a concentration of about 5 mM, about 10 mM or about 15 mM).

Preservatives

Optionally, in some embodiments, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation of the présent disclosure further comprises a preservative (e.g., an antimicrobial agent). Antimicrobial agents are generally required for parentéral products that are intended for multiple dosing. Similarly, preservatives are added to pharmaceutical formulations aseptically packaged in single dose vials if the active ingredient(s) does not hâve bactericidal or bacteriostatic properties or is growth promoting. Some typical preservatives used are benzyl alcohol (0.9% to 1.5%), methylparaben (0.18% to 0.2%), propylparaben (0.02%), benzalkonium chloride (0.01% to 0.02%), and thimerosal (0.001% to 0.01%).

Syringeability

The subcutaneous route of administration requires injections using injection devices, such as syringes, auto-injectors, wearable pumps, or other devices, which restricts product formulation with regard to injection volume and solution viscosity. In addition, product formulation must be suitable for use in an injection device with regard to injection force and time required for injection delivery. “Syringeablity,” as used herein, refers to the ability of an injectable therapeutic to pass easily through a hypodermic needle on transfer from a vial prior to an injection. “Injectability,” as used herein, refers to the performance of the formulation during injection (see, e.g., Cilurzo F, Selmin F, Minghetti P, et al. Injectability Evaluation: An Open Issue. AAPS PharmSciTech. 2011;12(2):604-609). Syringeability includes such factors as ease of withdrawal, clogging and foaming tendencies, and accuracy of dose measurements. Injectability includes pressure or force required for injection, evenness of flow, and freedom from clogging (i.e., no blockage of the syringe needle). Syringeability and injectability can be affected by the needle geometry, i.e., inner diameter, length, shape of the opening, as well as the surface finish of the syringe, especially in self-injection devices such as pens and auto-injectors (e.g., equipped with 29-31 GA needles), and in pre-filled syringes for subcutaneous dosing (e.g., equipped with 24-27 GA needles). Injection force (or glide force) is a complex factor influenced by solution viscosity, the size of the needle (i.e., needle gauge), and surface tension of the container/closure. Smaller needles, e.g., > gauge, will pose less pain sensation to patients. Overcashier and co-workers established a viscosity-glide force relationship as a function of needle gauge based on Hagen-Poiseuille Equation (Overcashier et al., Am Pharm Rev 9(6):77-83 (2006). For example, with a 27-gauge thin walled needle, the liquid viscosity should be maintained at or below 20 cP in order to not exceed the glide force of 25 Newton (N).

In certain embodiments, the pharmaceutical formulations of the invention are characterized by having an injection glide force of about 25N or less when injected through a 27GA (1.25”) needle at room température.

In certain embodiments, the pharmaceutical formulations of the invention are characterized by having an injection glide force of about 20N or less when injected through a 25GA (1”) needle at room température.

As exemplified in Example 3, the high-concentration, low-viscosity MASP-2 inhibitory antibody (e.g., OMS646) formulations of the présent disclosure hâve surprisingly good syringeability and injectability. The high-concentration, low-viscosity MASP-2 inhibitory antibody formulations as disclosed herein allow for the administration of such formulations by intramuscular or subcutaneous injection via small-bore needles typically used for such injections, for example, 27G (1.25”), 27G thin-walled, 25G thin-walled (1”), or 25G (1”) needles. In some instances, the low viscosity of MASP-2 inhibitory antibody formulations as disclosed herein allows for the administration of a tolerable (for example, 1 -3 cc) injected volume while delivering an effective amount of the MASP-2 inhibitory antibody in a single injection at a single injection site.

Stability

For any of the foregoing, it should be noted that the MASP-2 inhibitory antibody or antigen binding fragment thereof in the formulation retains the ability to inhibit MASP-219221 dépendent complément activation. For example, the MASP-2 inhibitory antibody retains the ability to bind MASP-2 and inhibit lectin pathway activity as described in Example l or other lectin pathway assay, for example as described in WO2012/151481. In addition to potency assays, varions physical-chemical assays can be used to assess stability including isoelectric focusing, polyacrylamide gel electrophoresis, size exclusion chromatography, and visible and subvisible particle assessment.

In certain embodiments, the formulations of the présent disclosure exhibit stability at a température range of -20°C to 8°C for at least 30 days, up to at least 9 months or longer, or up to at least 12 months or longer, as described in the stability studies in Examples 2 and 4. Additionally or altematively, in certain embodiments, the formulations are stable at the température of -20°C to 8° C, such as from 2°C to 8°C for at least 6 months, at least l year, or at least 2 years or longer. In certain embodiments, stability may be assessed, for example, by maintenance of a level of purity over time. For example, in certain embodiments, formulations of the présent disclosure hâve less than 5% decrease, such as less than 4% decrease, such as less than 3% decrease, such as less than 2%, such as less than 1% decrease in purity per month, 6 months, 9 months, or 1 year when stored at 2°C to 8°C, as determined by size exclusion chromatography (SEC), which monitors the presence or absence of fragments (LMW) and/or aggregate species (HMW).

In certain embodiments, the formulations of the présent disclosure promote low to undetectable levels of aggregation and/or fragmentation and maintain potency after storage for a defined period. Described another way, the formulations disclosed herein are capable of maintaining the structural integrity of the MASP-2 inhibitory antibody OMS646 présent at high concentrations in a solution, e.g., at concentrations of greater than 150 mg/mL, or greater than 175 mg/mL, or of at least 185 mg/mL, such that the MASP-2 inhibitory antibody can remain predominately monomeric (i.e., at least 95% or greater) after storage of a defined period at approximately 2°C to 8°C. Preferably, no more than 5%, no more than 4%, no more than 3%, no more than 2%, no more than 1%, and most preferably no more than 0.5% of the antibody forms fragment (LMW) or aggregate forms (HMW) as measured by SEC after storage of a defined period at approximately 2°C to 8°C.

As exemplified in Example 4 described herein, the inventors provide formulations suitable for maintaining a MASP-2 inhibitory antibody, OMS646, at about 185 mg/mL in predominately monomeric form for at least 12 months at about 2°C to 8°C.

Tissue Permeability Modifier

In another embodiment, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulations of the présent disclosure further comprise a tissue permeability modifier that increases the absorption or dispersion of the MASP-2 inhibitory antibody following parentéral administration (e.g., subcutaneous injection). In some embodiments, the tissue permeability modifier is a hyaluronidase enzyme which acts as a tissue permeability modifier and increases the dispersion and absorption of the injected MASP-2 inhibitory antibody. A particularly useful tissue permeability modifier is hyaluronidase (e.g., a recombinant human hyaluronidase). Hyaluronidases work as tissue permeability modifiers by temporarily breaking down the hyaluronan barrier to open access to the lymphatic and capillary vessels allowing injected drugs and fluids to be absorbed quickly into systemic circulation. The hyaluronan rebuilds naturally, and the barrier is completely restored, e.g., within 48 hours. Addition of hyaluronidase in the injectable pharmaceutical formulations increases bioavailability of the MASP-2 inhibitory antibody following parentéral administration, particularly subcutaneous administration. It also allows for greater injection site volumes (i.e., greater than 1 mL) with less pain and discomfort, and minimizes the incidence of injection site reactions (e.g., flattens the injection site bump).

In some embodiments, the high-concentration, low-viscosity MASP-2 inhibitory antibody (e.g., OMS646) formulation of the présent disclosure comprise from about 100 U/mL to about 20,000 U/mL of a hyaluronidase enzyme. The actual concentration of the hyaluronidase enzyme dépends on the type of hyaluronidase enzyme used in the préparation of the MASP-2 inhibitory antibody formulations of the présent invention. An effective amount of the hyaluronidase can be determined by the person skilled in the art. It should be provided in sufficient amount so that an increase in the dispersion and absorption of the coadministered or sequentially administered MASP-2 inhibitory antibody is possible. The minimal amount of the hyaluronidase enzyme is greater than 100 U/mL. More particularly, the effective amount of the hyaluronidase enzyme is from about 150U/mL to about 20,000U/mL, whereby the said amount corresponds to about 0.01 mg to 0.16 mg protein based on an assumed spécifie activity of 100,000 U/mg. In some embodiments, the pharmaceutical formulations comprise hyaluronidase in concentration of about Ι,θθθ to about 20,000 U/ml, such as about Ι,θθθ to about 16,000 U/ml. Altematively, the concentration of the hyaluronidase is about 1,500 to about 12,000 U/mL, or more particularly about 2,000 U/mL to about 12,000 U/mL. The amounts specified herein correspond to the amount of hyaluronidase initially added to the pharmaceutical formulation. In some embodiments, the ratio (w/w) of the hyaluronidase to the MASP-2 inhibitory antibody is in the range of 1:1,000 to 1:8,000, or in the range of 1:4,000 to 1:6,000 or in the range of about 1:4,000 to 1:5000.

The hyaluronidase may be présent as a component of the high-concentration, lowviscosity MASP-2 inhibitory antibody formulation of the présent disclosure, or it may be provided as a separate solution in a kit-of-parts. Thus, in one embodiment, the MASP-2 inhibitory antibody is co-formulated with a hyaluronidase. In another embodiment, the MASP-2 inhibitory antibody and hyaluronidase are formulated separately and mixed just prior to subcutaneous administration. In yet another embodiment, the MASP-2 inhibitory antibody and hyaluronidase are each formulated and administered separately, e.g., the hyaluronidase is administered as a separate injection directly before or after administration of the formulation comprising the MASP-2 inhibitory antibody. In some instances, the hyaluronidase is administered subcutaneously from about 5 seconds to about 30 minutes prior to the injection of the pharmaceutical formulation comprising the MASP-2 inhibitory antibody of the présent disclosure into the same injection site area. In certain embodiments, the pharmaceutical formulation of MASP-2 inhibitory antibody and hyaluronidase solution are included in separate chambers of a pharmaceutical device which automates delivery, either simultaneously (e.g., using a dual barrel syringe) or sequentially.

Pre-filled Containers

In a further aspect of the présent disclosure, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation as disclosed herein is contained in a pre-filled sealed container in an amount sufficient for administration to a mammalian subject. Thus a sufficient quantity of drug composition formulated in accordance with the présent disclosure, that is equal or just slightly more (i.e., not more than 25% excess, such as not more than 10% excess) than the amount of MASP-2 inhibitory antibody desired to be administered to a mammalian subject is contained within a pre-filled container that facilitâtes dispensing the antibody formulation for parentéral administration (i.e., injection or infusion). In some embodiments, the pre-filled container comprises at least one pharmaceutical unit dosage form of the MASP-2 inhibitory antibody.

For example, a desired single-use quantity of high-concentration, low-viscosity MASP-2 inhibitory antibody formulation may be packaged in pre-filled container, such as, for example, a glass vial closed with a stopper or other closure that includes a septum through which a hypodermic needle may be inserted to withdraw the formulation, or may be packaged in a pre-filled syringe or other pre-filled container suitable for injection (e.g., subcutaneous injection) or infusion. Examples of such containers include, without limitation, vials, syringes, ampoules, bottles, cartridges, and pouches. Preferably the containers are each single-use prefilled syringes, which may suitably be formed of glass or a polymeric material such as a cyclic olefin polymers or acrylonitrile butadiene styrene (ABS), polycarbonate (PC), polyoxymethylene (POM), polystyrène (PS), polybutylene terephthalate (PBT), polypropylene (PP), polyethylene (PE), polyamide (PA), thermoplastic elastomer (TPE), and their combinations. The barrels of such syringes are operated with an elastomer plunger which can be urged along the barrel to eject liquid content via a needle connected thereto. In some embodiments of the invention, each syringe includes a needle affixed thereto.

In some embodiments, the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation as disclosed herein is contained within a pre-filled container selected from the group consisting of: a syringe (e.g., a single or double barreled syringe), a pen injector, a sealed vial (e.g., a dual chamber vial), an auto-injector, a cassette, and a pump device (e.g., an on-body patch pump, a tethered pump or an osmotic pump). For subcutaneous delivery, the formulation may be contained within a pre-filled device suitable for subcutaneous delivery, such as, for example, a pre-filled syringe, autoinjector, injection device (e.g., the INJECT-EASE™, or GENJECT™ device), injector pen (such as the GENPEN™) or other device suitable for subcutaneous administration.

The formulations of the présent disclosure can be prepared as unit dosage forms in a pre-filled container, which can be particularly suitable for self-administration. For example, a unit dosage per vial, cartridge or other pre-filled container (e.g., pre-fdled syringe or disposable pen) may contain about O.l mL, 0.2 mL, 0.3 mL, 0.4 mL, 0.5 mL, 0.6 mL, 0.7 mL, 0.8 mL, 0.9 mL, 1 mL, 1.1 mL, 1.2 mL, 1.3 mL, 1.4 mL, 1.5 mL, 1.6 mL, 1.7 mL, 1.8 mL, 1.9 mL, 2.0 mL, 2.1 mL, 2.2 mL, 2.3 mL, 2.4 mL, 2.5 mL, 2.6 mL, 2.7 mL, 2.8 mL, 2.9 mL, 3.0 mL, 3.5 mL, 4.0 mL, 4.5 mL, 5.0 mL, 5.5 mL, 6.0 mL, 6.5 mL, 7.0 mL, 7.5 mL, 8.0 mL, 8.5 mL, 9.0 mL, 9.5 mL, or about 10.0 mL or greater volume of the high concentration formulation containing various concentrations of MASP-2 inhibitory antibody (e.g., OMS646) ranging from about 100 mg/mL to about 250 mg/mL, about 150 mg/mL to about 200 mg/mL, about 175 mg/mL to about 200 mg/mL, such as about 185 mg/mL, resulting in a total unit dosage of OMS646 per container ranging from about 20 mg to about 1000 mg or higher.

In some embodiments, the formulation of the présent disclosure is prepared as a unit dosage form in a pre-filled container, such as a vial or syringe, at a unit dosage of about

350mg to 400mg, such as about 350mg, about 360mg, about 370mg, about 380mg, about 390mg, or about 400mg.

In some embodiments, the formulations of the présent disclosure are prepared as unit dosage forms in a pre-filled syringe with a volume of from O.l mL to 3.0 mL, such as about 0.1 mL, 0.2 mL, 0.3 mL, 0.4 mL, 0.5 mL, 0.6 mL, 0.7 mL, 0.8 mL, 0.9 mL, 1 mL, 1.1 mL,

1.2 mL, 1.3 mL, 1.4 mL, 1.5 mL, 1.6 mL, 1.7 mL, 1.8 mL, 1.9 mL, 2.0 mL, 2.1 mL, 2.2 mL,

2.3 mL, 2.4 mL, 2.5 mL, 2.6 mL, 2.7 mL, 2.8 mL, 2.9 mL, or about 3.0 mL comprising from about 20 mg to 750 mg of the MASP-2 inhibitory antibody (e.g., OMS646). As described herein, the stable formulations prepared as unit dosages can be administered to a subject directly (e.g., via subcutaneous injection), or altematively are prepared to be suitable for dilution prior to intravenous administration.

The formulations of the présent disclosure may be sterilized by various sterilization methods suitable for antibody formulations, such as stérile filtration. In certain embodiments the antibody formulation is filter-sterilized, for example, with a presterilized 0.2 micron filter. Sterilized formulations of the présent disclosure may be administered to a subject to prevent, treat or ameliorate a disease or disorder associated with MASP-2-dependent complément activation.

In a related aspect, the présent disclosure provides a method of making an article of manufacture comprising filing a container with a high concentration MASP-2 inhibitory antibody formulation of the présent disclosure.

In one embodiment, the présent disclosure provides a pharmaceutical composition for use in treating a patient suffering from, or at risk for developing a MASP-2-dependent disease or condition, wherein the composition is a stérile, single-use dosage form comprising from about 350 mg to about 400 mg (i.e., 350 mg, 360 mg, 370 mg, 380 mg, 390 mg, or 400 mg) of MASP-2 inhibitory antibody, wherein the composition comprises about 1.8mL to about 2.2 mL (i.e., 1.8 mL, 1.9mL, 2.0 mL, 2.1 mL or 2.2 mL) of a 185 mg/mL antibody formulation, such as disclosed herein, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising the amino acid sequence set forth in SEQ ID NO:2 and (ii) a light chain variable région comprising the amino acid sequence set forth in SEQ ID NO:3; and wherein the formulation is stable when stored at between 2°C and 8°C for at least six months. In some embodiments, the MASP-2 dépendent disease or condition is selected from the group consisting of aHUS, HSCT-TMA, IgAN and Lupus Nephritis (LN).

Kits comprising high-concentration, low-viscosity MASP-2 inhibitory antibody formulations

The présent disclose also features therapeutic kits comprising at least one container including the high-concentration, low-viscosity MASP-2 inhibitory antibody formulation as disclosed herein.

In some embodiments, the présent disclosure provides a kit comprising (i) a container comprising any of the formulations comprising MASP-2 inhibitory antibody described herein; and (ii) a suitable means for delivering the formulation to a patient in need thereof. In some embodiments of any of the kits described herein, the means is suitable for subcutaneous delivery of the formulation to the patient.

Various types of containers are suitable for containment of pharmaceutical formulations of MASP-2 inhibitory antibody included in the kits of the présent invention. In certain embodiments of the kits of the présent invention, the container is a prefilled syringe (e.g., a single barrel or double-barreled syringe) or a prefilled sealed viaL

In some embodiments, the container comprising a formulation comprising MASP-2 inhibitory antibody is a pre-filled container selected from the group consisting of: a syringe (e.g., a single or double barreled syringe), a pen injector, a sealed vial (e.g., dual chamber vials), an auto-injector, a cassette, and a pump device (e.g., an on-body patch pump or a tethered pump or an osmotic pump). For subcutaneous delivery, the formulation may be contained within a pre-filled device suitable for subcutaneous delivery, such as, for example, a pre-filled syringe, autoinjector, injection device (e.g., the INJECT-EASE™, and GENJECT™ device), injector pen (such as the GENPEN™) or other device suitable for subcutaneous administration.

In addition to a container pre-filled with a single-dose of the pharmaceutical formulation, the kit of the présent invention may also include an outer container into which such pre-filled container is placed. For example, the outer container may include a plastic or paperboard tray into which recesses are formed that receive the pre-filled container and immobilize it during shipping and handling prior to use. In some embodiments, the outer container is suitably opaque and acts to shield the pre-filled container from light to prevent light induced dégradation of the components of the pharmaceutical formulation. For example, the plastic or paperboard tray that receives pre-filled container may be further packaged within a paperboard carton that provides light shielding. The kit of the présent invention may also include a set of instructions for administration and use of the MASP-2 inhibitory antibody formulations in accordance with the présent invention, which may be printed on the outer container or printed on a sheet of paper that is contained within the outer container.

In some embodiments, the kits comprise a second container (e.g., a prefilled syringe) containing an effective dose of a hyaluronidase.

The kit may further include other materials désirable from a commercial and user standpoint, including needles, syringes, package inserts and the like.

Exemplary Formulations

As described above, the stable, high-concentration, low-viscosity MASP-2 inhibitory antibody formulations of the présent disclosure include MASP-2 inhibitory antibody a concentration of from 50 mg/mL to 250 mg/mL in an aqueous solution comprising a buffering agent having a pH of 4.0 to 8.0.

The buffer System, such as histidine, citrate or succinate, is suitably included at a concentration of from about 10 mM to about 50 mM, and preferably at about 20 mM. In some preferred embodiments, the formulation further comprises an amino acid with a charged side chain at a concentration of from 50 mM to 300 mM. In some embodiments, the formulation comprises an amino acid with a positively charged side chain, such as arginine, at a concentration of from 50 mM to 300 mM. In some preferred embodiments, the formulation further comprises a non-ionic surfactant, such as polysorbate 80, in an amount from 0.001 % (w/v) to 0.1 % (w/v), such as about 0.05% (w/v) to about 0.1% (w/v). In some embodiments, the formulation further comprises a hyaluronidase enzyme in an amount effective to increase the dispersion and/or absorption of the MASP-2 inhibitory antibody following subcutaneous administration.

In some embodiments the stable high-concentration, low-viscosity MASP-2 inhibitory antibody formulations of the présent disclosure comprise, consist of, or consist essentially of one of the following compositions:

a) 100 to 200 mg/mL MASP-2 inhibitory antibody; 10 to 50 mM of a histidine buffer at a pH of about 5.0 to about 7.0; 100 mM to 225 mM arginine; and optionally 100 to 20,000 U/mL of a hyaluronidase.

b) 100 to 200 mg/mL MASP-2 inhibitory antibody; 10 to 50 mM of a histidine buffer at a pH of about 5.0 to about 7.0; 100 mM to 225 mM arginine, about 0.01% to 0.08% (w/v) of a nonionic surfactant; and optionally 100 to 20,000 U/mL of a hyaluronidase.

c) 100 to 200 mg/mL MASP-2 inhibitory antibody; 10 to 50 mM of a citrate buffer at a pH of about 5.0 to about 7.0; 100 mM to 225 mM arginine, and optionally 100 to 20,000 U/mL of a hyaluronidase.

d) 100 to 200 mg/mL MASP-2 inhibitory antibody; 10 to 50 mM of a citrate buffer at a pH of about 5.0 to about 7.0; 100 mM to 225 mM arginine, about 0.01% to 0.08% (w/v) of a nonionic surfactant; and optionally 100 to 20,000 U/mL of a hyaluronidase.

e) 100 to 200 mg/mL MASP-2 inhibitory antibody; 10 to 50 mM of a succinate buffer at a pH of about 5.0 to about 7.0; 100 mM to 225 mM arginine, and optionally 100 to 20,000 U/mL of a hyaluronidase.

f) 100 to 200 mg/mL MASP-2 inhibitory antibody; 10 to 50 mM of a succinate buffer at a pH of about 5.0 to about 7.0; 100 mM to 225 mM arginine, about 0.01% to 0.08% (w/v) of a nonionic surfactant; and optionally 100 to 20,000 U/mL of a hyaluronidase.

In certain embodiments, the stable high-concentration, low-viscosity MASP-2 inhibitory antibody formulations of the présent disclosure comprise, consist of, or consist essentially of one of the following compositions:

g) 185+18.5 mg/mL MASP-2 inhibitory antibody; 20±2 mM citrate buffer at a pH of about 5.8; 200+20 mM arginine, and optionally 100 to 20,000 U/mL of a hyaluronidase.

h) 185+18.5 mg/mL MASP-2 inhibitory antibody; 20+2 mM citrate buffer at a pH of about 5.8; 200+20 mM arginine, about 0.01% (w/v) polysorbate 80, and optionally 100 to 20,000 U/mL of a hyaluronidase.

i) 185+18.5 mg/mL MASP-2 inhibitory antibody; 20+2 mM histidine buffer at a pH of about 5.9, 200+20 mM arginine, and optionally 100 to 20,000 U/mL of a hyaluronidase.

j) 185+18.5 mg/mL MASP-2 inhibitory antibody; 20+2 mM histidine buffer at a pH of about 5.9, 200+20 mM arginine, about 0.01% polysorbate 80, and optionally 100 to 20,000 U/mL of a hyaluronidase.

Methods of producing high-concentration, low-viscosity MASP-2 inhibitory antibody formulations

In another aspect, the présent disclosure provides a method for producing a formulation comprising 100 mg/mL or greater of a MASP-2 inhibitory antibody, the method comprising: (a) providing a first pharmaceutical formulation comprising purified OMS646, the first pharmaceutical formulation having a first formulation and comprising no more than 50 mg/mL of the OMS646 protein; (b) subjecting the first pharmaceutical formulation to filtration to thereby produce a second pharmaceutical formulation, wherein the second 5 pharmaceutical formulation has a second formulation as a resuit of the filtration; and (c) concentrating the second pharmaceutical formulation to produce a concentrated antibody solution comprising 100 mg/mL or greater of OMS646. The formulated bulk solution is typically set at a fixed protein concentration so that the desired fill volume can be kept constant. The liquid drug product manufacturing process typically involves mixing the 10 MASP-2 inhibitory antibody with the buffering System, excipients and optionally surfactant, followed by aseptie filtration and filling in vials (or other container, such as syringes) and sealing (e.g., stoppering, capping, or the like).

TABLE 1: Example Formulation 1

Component (USP) added to water for injection	Concentration
OMS646 antibody	185 mg/mL
Sodium Citrate	20 mM
L-Arginine HCL	200 mM
Polysorbate 80	0.01%

TABLE 2: Example Formulation 2

Component (USP) added to water for injection	Concentration
OMS646 antibody	185 mg/mL
L-Histidine	20 mM
L-Arginine HCL	200 mM
Polysorbate 80	0.01%

Methods of Treatment

In another aspect, the présent disclosure provides a method of treating a patient suffering from, or at risk for developing a MASP-2-dependent complement-associated disease or disorder comprising administering a high concentration low viscosity formulation comprising a MASP-2 inhibitory antibody (e.g., OMS646) as disclosed herein.

As described in U.S. Patent No. 7,919,094; U.S. Patent No. 8,840,893; U.S. Patent No. 8,652,477; U.S. Patent No. 8,951,522, U.S. Patent No. 9,011,860, U.S. Patent No. 9,644,035, U.S. Patent Application Publication Nos. US2013/0344073, US2013/0266560, US 2015/0166675, US2017/0137537, US2017/0189525 and co-pending U.S. Patent Application Serial Nos. 15/476,154, 15/347,434, 15/470,647, 62/315,857, 62/275,025 and 62/527,926 (each of which is assigned to Omeros Corporation, the assignée of the instant application, each of which is hereby incorporated by reference), MASP-2-dependent complément activation has been implicated as contributing to the pathogenesis of numerous acute and chronic disease states. For example, as described in U.S. Patent No. 8,951,522, the primary function of the complément System, a part of the innate immune System, is to protect the host against infectious agents, however, inappropriate or over-activation of the complément System can lead to serious disease, such as thrombotic microangiopathies (TMAs, including aHUS, TTP and EUS) in which endothélial damage as well as fibrin and platelet-rich thrombi in the microvasculature lead to organ damage. The lectin pathway plays a dominant rôle in activating complément in settings of endothélial cell stress or injury, and preventing the activation of MASP-2 and the lectin pathway halts the sequence of enzymatic reactions that lead to the formation of the membrane attack complex, platelet activation and leukocyte recruitment. As described in U.S. Patent No. 8,652,477, in addition to initiation of the lectin pathway, MASP-2 can also activate the coagulation System and is capable of cleaving prothrombin to thrombin.

As described in Example 1 and U.S. Patent No. 9,011,860, OMS646 is a potent inhibitor of lectin-dependent complément activation. This antibody shows no significant binding (at least 5000-fold lower affinity) to the other complément pathway serine proteases Clr, Cl s, MASP-1 and MASP-3, and does not inhibit classical pathway dépendent complément activation.

Accordingly, in some embodiments, the method comprises administering to a patient suffering from or a risk for developing a MASP-2-dependent complement-associated disease or disorder an amount of any of the high-concentration, low-viscosity MASP-2 inhibitory antibody formulations disclosed herein in an amount sufficient to inhibit MASP-2 dépendent complément activation in said mammalian subject to thereby treat the disease or disorder. In some embodiments, the methods can be performed using any of the kits or pre-filled containers (e.g., pre-filled syringes or vials) described herein. In some embodiments, the method can further comprise, prior to administering the formulation to the patient, determining that the patient is afflicted with the lectin complement-associated disease or disorder. In some embodiments, the method further comprises administering a tissue permeability modifier (e.g., hyaluronidase) that increases the absorption or dispersion of the MASP-2 inhibitory antibody following parentéral administration. The tissue permeability modifier may be co-administered with the MASP-2 inhibitory antibody formulation or administered sequentially (e.g., within 5 minutes of administering the MASP-2 inhibitory antibody formulation at or near the same injection site).

In some embodiments, the method comprises injecting a subject in need thereof from a first prefilled syringe containing a high concentration low viscosity formulation comprising MASP-2 inhibitory antibody (e.g., OMS646) to inhibit MASP-2-dependent complément activation. In some embodiments, the method further comprises injecting the subject from a second pre-filled syringe containing a tissue permeability modifier, wherein the injection is at or near the site of the injection with the MASP-2 inhibitory antibody.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a thrombotic microangiopathy (TMA) including thrombotic thrombocytopénie purpura (TTP), refractory TTP, Upshaw-Schulman Syndrome (USS), hemolytic urémie syndrome (HUS), atypical hemolytic syndrome (aHUS), non-Factor H-dependent atypical hemolytic syndrome, aHUS secondary to an infection, plasma therapy-resistant aHUS, a TMA secondary to cancer, a TMA secondary to chemotherapy, a TMA secondary to transplantation, or a TMA associated with hematopoietic stem cell transplant.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a rénal condition including, but not limited to, mesangioproliferative glomerulonephritis, membranous glomerulonephritis, membranoproliferative glomerulonephritis (mesangiocapillary glomerulonephritis), acute post infectious glomerulonephritis (poststreptococcal glomerulonephritis), C3 glomerulopathy, cryoglobulinémie glomerulonephritis, pauci-immune necrotizing crescentic glomerulonephritis, lupus nephritis, Henoch-Schonlein purpura nephritis and IgA nephropathy.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is rénal fibrosis (e.g., tubulointerstitial fibrosis) and/or proteinuria in a subject suffering from or at risk for developing chronic kidney disease, chronic rénal failure, glomerular disease (e.g., focal segmentai glomerulosclerosis), an immune complex disorder (e.g., IgA nephropathy, membranous nephropathy), lupus nephritis, nephrotic syndrome, diabetic nephropathy, tubulointerstitial damage and glomerulonepthritis (e.g., C3 glomerulopathy), or a disease or condition associated with proteinuria, including, but not limited to nephrotic syndrome, pre-eclampsia, eclampsia, toxic lésions of kidneys, amyloidosis, collagen vascular diseases (e.g., systemic lupus erythematosus), déhydration, glomerular diseases (e.g., membranous glomerulonephritis, focal segmentai glomerulonephritis, C3 glomerulopathy, minimal change disease, lipoid nephrosis), strenuous exercise, stress, benign orthostatis (postural) proteinuria, focal segmentai glomerulosclerosis, IgA nephropathy (i.e., Berger’s disease), IgM nephropathy, membranoproliferative glomerulonephritis, membranous nephropathy, minimal change disease, sarcoidosis, Alport’s syndrome, diabètes mellitus (diabetic nephropathy), drug-induced toxicity (e.g., NSAIDS, nicotine, penicillamine, lithium carbonate, gold and other heavy metals, ACE inhibitors, antibiotics (e.g., adriamycin) or opiates (e.g., heroin) or other nephrotoxins); Fabry’s disease, infections (e.g., HIV, syphilis, hepatitis A, B or C, poststreptococcal infection, urinary schistosomiasis); aminoaciduria, Fanconi syndrome, hypertensive nephrosclerosis, interstitial nephritis, sickle cell disease, hemoglobinuria, multiple myeloma, myoglobinuria, organ rejection (e.g., kidney transplant rejection), ebola hémorrhagie fever, Nail patella syndrome, familial mediterranean fever, HELLP syndrome, systemic lupus erythematosus, Wegener’s granulomatosis, Rheumatoid arthritis, Glycogen storage disease type 1, Goodpasture’s syndrome, Henoch-Schonlein purpura, urinary tract infection which has spread to the kidneys, Sjôgren’s syndrome and post-infections glomerulonepthritis.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an inflammatory reaction resulting from tissue or solid organ transplantation including, but not limited to, allotransplantation or xenotransplantation of whole organs {e.g., kidney, heart, liver, pancréas, lung, cornea, and the like) or tissue grafts (e.g., valves, tendons, bone marrow, and the like).

In some embodiments, the MASP-2-dependent complement-associated disorder is an ischemia reperfusion injury (I/R), including but not limited to, myocardial I/R, gastrointestinal I/R, rénal I/R, and I/R following an aortic aneurism repair, I/R associated with cardiopulmonary bypass, cérébral I/R, stroke, organ transplant or reattachment of severed or traumatized limbs or digits; revascularization to transplants and/or replants, and hémodynamie resuscitation following shock and/or surgical procedures.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a complication associated with non-obese diabètes (Type-1 diabètes or Insulindependent diabètes mellitus) and/or complications associated with Type-1 or Type-2 (adult onset) diabètes including, but not limited to diabetic angiopathy, diabetic neuropathy, diabetic retinopathy or diabetic macular edema.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a cardiovascular disease or disorder, including but not limited to, Henoch-Schonlein purpura nephritis, systemic lupus erythematosus-associated vasculitis, vasculitis associated with rheumatoid arthritis (also called malignant rheumatoid arthritis), immune complex vasculitis, and Takayasu's disease; dilated cardiomyopathy; diabetic angiopathy; Kawasaki's disease (arteritis); venous gas embolus (VGE); and inhibition of restenosis following stent placement, rotational atherectomy and/or percutaneous transluminal coronary angioplasty (PTCA).

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an inflammatory gastrointestinal disorder, including but not limited to, pancreatitis, diverticulitis and bowel disorders including Crohn's disease, ulcerative colitis, irritable bowel syndrome and inflammatory bowel disease (IBD).

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a pulmonary disorder, including but not limited to, acute respiratory distress syndrome, transfusion-related acute lung injury, ischemia/reperfusion acute lung injury, chronic obstructive pulmonary disease, asthma, Wegener's granulomatosis, antiglomerular basement membrane disease (Goodpasture's disease), méconium aspiration syndrome, aspiration pneumonia, bronchiolitis obliterans syndrome, idiopathic pulmonary fibrosis, acute lung injury secondary to bum, non-cardiogenic pulmonary edema, transfusion-related respiratory dépréssion and emphysema.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a extracorporeal exposure-triggered inflammatory reaction and the method comprises treating a subject undergoing an extracorporeal circulation procedure including, but not limited to, hemodialysis, plasmapheresis, leukopheresis, extracorporeal membrane oxygénation (ECMO), heparin-induced extracorporeal membrane oxygénation LDL précipitation (HELP) and cardiopulmonary bypass (CPB).

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is inflammatory or non-inflammatory arthritides and other musculoskeletal disorders, including but not limited to, osteoarthritis, rheumatoid arthritis, juvénile rheumatoid arthritis, goût, neuropathie arthropathy, psoriatic arthritis, ankylosing spondylitis or other spondyloarthropathies and crystalline arthropathies, muscular dystrophy and systemic lupus erythematosus (SLE).

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a skin disorder, including, but not limited to, psoriasis, autoimmune bullous dermatoses, éosinophilie spongiosis, bullous pemphigoid, epidermolysis bullosa acquisita, atopie dermatitis, herpes gestationis and other skin disorders, and for the treatment of thermal and chemical burns including capillary leakage caused thereby.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a peripheral nervous System (PNS) and/or central nervous System (CNS) disorder or injury including, but not limited to, multiple sclerosis (MS), myasthenia gravis (MG), Huntington's disease (HD), amyotrophie latéral sclerosis (ALS), Guillain Barre syndrome, reperfusion following stroke, degenerative dises, cérébral trauma, Parkinson's disease (PD), Alzheimer's disease (AD), Miller-Fisher syndrome, cérébral trauma and/or hemorrhage, traumatic brain injury, demyelination and meningitis.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is sepsis or a condition resulting from sepsis including without limitation severe sepsis, septic shock, acute respiratory distress syndrome resulting from sepsis, hemolytic anémia, systemic inflammatory response syndrome, or hémorrhagie shock.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is a urogénital disorder including, but not limited to, painful bladder disease, sensory bladder disease, chronic abacterial cystitis and interstitial cystitis, male and female infertility, placental dysfunction and miscarriage and pre-eclampsia.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an inflammatory reaction in a subject being treated with chemotherapeutics and/or radiation therapy, including without limitation for the treatment of cancerous conditions.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an angiogenesis-dependent cancer, including but not limited to, a solid tumor(s), blood borne tumor(s), high-risk carcinoid tumors and tumor métastasés.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an angiogenesis-dependent benign tumor, including but not limited to hemangiomas, acoustic neuromas, neurofibromas, trachomas, carcinoid tumors and pyogénie granulomas.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an endocrine disorder including, but not limited to, Hashimoto's thyroiditis, stress, anxiety and other potential hormonal disorders involving regulated release of prolactin, growth or insulin-like growth factor, and adrenocorticotropin from the pituitary.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an ophthalmic disease or disorder including, but not limited to age-related macular degeneration, glaucoma and endophthalmitis.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is an ocular angiogenic disease or condition including, but not limited to age-related macular degeneration, uveitis, ocular melanoma, comeal neovascularization, primary pterygium, HSV stromal keratitis, HSV-l-induced comeal lymphangiogenesis, proliférative diabetic retinopathy, diabetic macular edema, retinopathy of prematurity, retinal vein occlusion, corneal graft rejection, neovascular glaucoma, vitreous hemorrhage secondary to proliférative diabetic retinopathy, neuromyelitis optica and rubeosis.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is disseminated intravascular coagulation (DIC) or other complément mediated coagulation disorder, including DIC secondary to sepsis, severe trauma, including neurological trauma (e.g., acute head injury, see Kumura et al., Acta Neurochirurgica 85:2328 (1987), infection (bacterial, viral, fungal, parasitic), cancer, obstétrical complications, liver disease, severe toxic reaction (e.g., snake bite, insect bite, transfusion reaction), shock, heat stroke, transplant rejection, vascular aneurysm, hepatic failure, cancer treatment by chemotherapy or radiation therapy, bum, or accidentai radiation exposure.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is selected from the group consisting of acute radiation syndrome, dense deposit disease, Degos Disease, Catastrophic Antiphospholipid Syndrome (CAPS), Behcet’s disease, cryoglobulinemia; paroxysmal noctumal hemoglobinuria (PNH) and cold agglutinin disease.

In some embodiments, the MASP-2-dependent complement-associated disease or disorder is selected from the group consisting of aHUS, HSCT-TMA, IgAN, and Lupus Nepthritis (LN).

Atypical hemolytic urémie syndrome (aHUS)

Atypical hemolytic urémie syndrome (aHUS) is part of a group of conditions termed “Thrombotic microangiopathies.” In the atypical form of HUS (aHUS), the disease is associated with defective complément régulation and can be either sporadic or familial. Familial cases of aHUS are associated with mutations in genes coding for complément activation or complément regulatory proteins, including complément factor H, factor I, factor B, membrane cofactor CD46 as well as complément factor H-related protein 1 (CFHR1) and complément factor H-related protein 3 (CFHR3). (Zipfel, P.F., et al., PloS Genetics 3(3):e41 (2007)). The unifying feature of this diverse array of genetic mutations associated with aHUS is a prédisposition to enhanced complément activation on cellular or tissue surfaces. A subject is a risk for developing aHUS upon the onset of at least one or more symptoms indicative of aHUS (e.g., the presence of anémia, thrombocytopenia and/or rénal insufficiency) and/or the presence of thrombotic microangiopathy in a biopsy obtained from the subject. The détermination of whether a subject is at risk for developing aHUS comprises determining whether the subject has a genetic prédisposition to developing aHUS, which may be carried out by assessing genetic information (e.g. from a database containing the génotype of the subject), or performing at least one genetic screening test on the subject to détermine the presence or absence of a genetic marker associated with aHUS (i.e., determining the presence or absence of a genetic mutation associated with aHUS in the genes encoding complément factor H (CFH), factor I (CFI), factor B (CFB), membrane cofactor CD46, C3, complément factor H-related protein 1 (CFHR1), or THBD (encoding the anticoagulant protein thrombodulin) or complément factor H-related protein 3 (CFHR3), or complément factor H-related protein 4 (CFHR4)) either via genome sequencing or gene-specific analysis (e.g., PCR analysis), and/or determining whether the subject has a family history of aHUS. Methods of genetic screening for the presence or absence of a genetic mutation associated with aHUS are well established, for example, see Noris M et al. “Atypical Hemolytic-Uremic Syndrome,” 2007 Nov 16 [Updated 2011 Mar 10]. In: Pagon RA, Bird TD, Dolan CR, et al., editors. GeneReviews™, Seattle (WA): University of Washington, Seattle.

As described in US2015/0166675, in a human ex vivo experimental model of thrombotic microangiopathy (TMA), OMS646 inhibited complément activation and thrombus formation on microvascular endothélial cells exposed to sérum samples from aHUS patients in both the acute phase and in remission. As further described in US2017/0137537, data obtained in an open-label Phase 2 clinical trial (i.v. administration of 2-4 mg/kg MASP-2 inhibitory antibody OMS646 once per week for 4 consecutive weeks), treatment with OMS646 showed efficacy in patients with aHUS. Platelet counts in ail three aHUS patients in the mid- and high-dose cohorts (two in the mid-dose and one in the high-dose cohort) returned to normal, with a statistically significant mean increase from baseline of approximately 68,000 platelets/mL (p=0.0055).

Hematopoietic stem cell transplant-associated TMA fHSCT-TMA)

Hematopoietic stem cell transplant-associated TMA (HSCT-TMA) is a lifethreatening complication that is triggered by endothélial injury. The kidney is the most commonly affected organ, though HSCT-TMA can be a multi-system disease that also involves the lung, bowel, heart and brain. The occurrence of even mild TMA is associated with long-term rénal impairment. Development of post-allogeneic HSCT-associated TMA differs in frequency based on varying diagnostic criteria and conditioning and graft-versushost disease prophylaxis regimens, with calcineurin inhibitors being the most frequent drugs implicated (Ho VT et al., Biol Blood Marrow Transplant, 11(8):571-5, 2005).

As described in US2017/0137537, in an Phase 2 clinical trial (i.v. administration of 4 mg/kg MASP-2 inhibitory antibody OMS646 once per week for 4 to 8 consecutive weeks), treatment with OMS646 improved TMA markers in patients suffering from HSCT-TMA, including a statistically significant improvement in LDH and haptoglobin levels. The HSCTTMA patients treated with OMS646 represent some of the most difficult to treat, thereby demonstrating clinical evidence of a therapeutic effect of OMS646 in patients with HSCTTMA.

Immunoglobulin A nephropathy (IgAN)

Immunoglobulin A nephropathy (IgAN) is an auto immune kidney disease resulting in intrarenal inflammation and kidney injury. IgAN is the most common primary glomerular disease globally. With an annual incidence of approximately 2.5 per 100,000, it is estimated that 1 in 1400 persons in the U.S. will develop IgAN. As many as 40% of patients with IgAN will develop end-stage rénal disease (ESRD). Patients typically présent with microscopie hematuria with mild to moderate proteinuria and variable levels of rénal insufficiency (Wyatt R.J., et al., N Engl J Med 368(25):2402-14, 2013). Clinical markers such as impaired kidney function, sustained hypertension, and heavy proteinuria (over 1 g per day) are associated with poor prognosis (Goto M et aL, Nephrol Dial Transplant 24(10):3068-74, 2009; Berthoux F. et aL, J Am Soc Nephrol 22(4):752-61, 2011). Proteinuria is the strongest prognostic factor independent of other risk factors in multiple large observational studies and prospective trials (Coppo R. et al., J Nephrol 18(5):503-12, 2005; Reich H. N., et aL, J Am Soc Nephrol 18(12):3177-83, 2007). It is estimated that 15-20% of patients reach ESRD within 10 years of disease onset if left untreated (D’Amico G., Am JKidney Dis 36(2):227-37, 2000). The diagnostic hallmark of IgAN is the prédominance of IgA deposits, alone or with IgG, IgM, or both, in the glomerular mesangium.

As described in US2017/0189525, in a Phase 2 open-label rénal trial (i.v. administration of 4 mg/kg MASP-2 inhibitory antibody OMS646 once per week for 12 consecutive weeks), patients with IgA nephropathy that were treated with OMS646 demonstrated a clinically meaningful and statistically significant decrease in urine albuminto-creatinine ratios (uACRs) throughout the trial and réduction in 24-hour urine protein levels from baseline to the end of treatment.

Lupus Nephritis (LN)

A main complication of systemic lupus erythematosus (SLE) is nephritis, also known as lupus nephritis, which is classified as a secondary form of glomerulonephritis. Up to 60% of adults with SLE hâve some form of kidney involvement later in the course of the disease (Koda-Kimble et al., Koda-Kimble and Young’s Applied Therapeutics: the clinical use of drugs, 10^th Ed, Lippincott Williams & Wilkins: pages 792-9, 2012) with a prevalence of 2070 per 100,000 people in the US. Lupus nephritis often présents in patients with other symptoms of active SLE, including fatigue, fever, rash, arthritis, serositis, or central nervous System disease (Pisetsky D.S. et al., Med Clin North Am 81(1):113-28, 1997). Some patients hâve asymptomatic lupus nephritis; however, during regular follow-up, laboratory abnormalities such as elevated sérum créatinine levels, low albumin levels, or urinary protein or sédiment suggest active lupus nephritis.

As described in U.S. Patent Application No. 15/470,647, in a Phase 2 open-label rénal trial (i.v. administration of 4 mg/kg MASP-2 inhibitory antibody OMS646 once per week for 12 consecutive weeks), 4 out of 5 patients with Lupus Nephritis (LN) that were treated with an anti-MASP-2 antibody demonstrated a clinically meaningful decrease in 24-hour urine protein levels from baseline to the end of treatment.

Administration

The high concentration low viscosity MASP-2 inhibitory antibody formulations described herein can be administered to a subject in need of treatment using methods known in the art, such as by single or multiple injections or infusions over a period of time in a suitable manner, e.g., injection or infusion by subcutaneous, intravenous, intraperitoneal, intramuscular. As described herein, parentéral formulations can be prepared in dosage unit form for ease of administration and uniformity of dosage. As used herein the term “unit dosage form” refers to physically discrète units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the selected pharmaceutical aqueous solution .

For the prévention or treatment of disease, the appropriate dosage of the MASP-2 inhibitory antibody will dépend on the type of disease to be treated, the severity and course of the disease. The antibody is suitably administered to the patient at one time or over a sériés of treatments. Depending on the type and severity of the disease, the MASP-2 inhibitory antibody can be administered at a fixed dose, or in a milligram per kilogram (mg/kg) dose. Exemplary dosages of the MASP-2 inhibitory antibody contained in the formulations described herein include, e.g., about 0.05 mg/kg to about 20 mg/kg, such as about 1 mg/kg, 2 mg/kg, 3 mg/kg, 4 mg/kg, 5 mg/kg, 6 mg/kg, 7 mg/kg, 8 mg/kg, 9 mg/kg, 10 mg/kg, 11 mg/kg, 12 mg/kg, 13 mg/kg, 14 mg/kg, 15 mg/kg, 16 mg/kg, 17 mg/kg, 18 mg/kg, 19 mg/kg or 20 mg/kg which can be administered daily, twice weekly, once weekly, bi-weekly, or monthly.

Exemplary fixed dosages of the MASP-2 inhibitory antibody, such as the formulations described herein include, e.g., about 10 mg to about 1000 mg, such as about 50 mg to about 750 mg, such as about 100 mg to about 500 mg, such as about 200 mg to about 400 mg, such as about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, or about 400 mg which can be administered daily, twice weekly, once weekly, bi-weekly, or monthly.

With regard to delivery volume of the formulations, the concentration of the antibody in a formulation used for a therapeutic application is determined based on providing the antibody in a dosage and volume that is tolerated by, and of therapeutic value to, the patient. For a therapeutic antibody formulation to be administered by injection, the antibody concentration will be dépendent on the injection volume (usually from 0.5 mL to 3 mL). Antibody based thérapies can require several mg/kg of dosing per day, per week, per month, or per several months. Accordingly, if a MASP-2 inhibitory antibody is to be provided at Img/kg to 5 mg/kg (e.g., Img/kg, 2 mg/kg, 3 mg/kg, 4 mg/kg or 5 mg/kg) of body weight of the patient, and an average patient weighs 75 kg, then 75 mg to 375 mg of the antibody will need to be delivered in a 0.5 mL to 3.0 mL injection volume. Altematively, the formulation is provided in a concentration suitable for delivery at more than one injection site per treatment.

In a preferred embodiment in which the concentration of the OMS646 antibody in the formulation is about 185 mg/mL, for a dosage of 1 mg/kg to 5 mg/kg of body weight of the patient (assuming 75 kg), the formulation would be delivered subcutaneously in about 0.40 mL to about 2.0 mL injection volume.

As described herein, the formulations of the présent disclosure are suitable for both intravenous (i.v.) dosage and subcutaneous (s.c.) administration.

Depending on the type and severity of the disease, the MASP-2 inhibitory antibody can be administered intravenously at a fixed dose, or in a milligram per kilogram (mg/kg) dose. Exemplary dosages of the MASP-2 inhibitory antibody contained in the formulations described herein can be delivered intravenously by diluting an appropriate amount of the high concentration formulation described herein with a pharmaceutically acceptable diluent prior to administration such that the MASP-2 inhibitory antibody is administered to a human subject at a dosage of e.g., about 0.05 mg/kg to about 20 mg/kg, such as about 1 mg/kg, 2 mg/kg, 3 mg/kg, 4 mg/kg, 5 mg/kg, 6 mg/kg, 7 mg/kg, 8 mg/kg, 9 mg/kg, 10 mg/kg, 11 mg/kg, 12 mg/kg, 13 mg/kg, 14 mg/kg, 15 mg/kg, 16 mg/kg, 17 mg/kg, 18 mg/kg, 19 mg/kg or 20 mg/kg which can be administered daily, twice weekly, once weekly, bi-weekly, or monthly.

The MASP-2 inhibitory antibody can also be delivered intravenously at a fixed dosage by diluting an appropriate amount of the high concentration formulation described herein with a pharmaceutically acceptable diluent prior to administration such that the MASP-2 inhibitory antibody is administered to a human subject at a dosage of about 10 mg to about 1000 mg, such as about 50 mg to about 750 mg, such as about 100 mg to about 500 mg, such as about 200 mg to about 400 mg, such as about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, such as about 300 mg to about 400 mg, such as about 310 mg, about 320 mg, about 325 mg, about 330 mg, about 340 mg, about 350 mg, about 360 mg, about 370 mg, about 375 mg, about 380 mg, about 390 mg or about 400 mg which can be administered daily, twice weekly, once weekly, bi-weekly, or monthly.

In some embodiments, the formulation comprising the MASP-2 inhibitory antibody is diluted into a pharmaceutically-acceptable diluent prior to systemic (e.g., intravenous) delivery. Exemplary diluents which can be used include water for injection, 5% dextrose, 0.9% saline, Ringers solution and other pharmaceutically-acceptable diluents suitable for intravenous delivery. While in no way intended to be limiting, exemplary dosages of a MASP-2 inhibitory antibody to be administered intravenously to treat a subject suffering from a MASP-2-dependent complément disease or disorder include, e.g., about 0.05 mg/kg to about 20 mg/kg, such as about l mg/kg, 2 mg/kg, 3 mg/kg, 4 mg/kg, 5 mg/kg, 6 mg/kg, 7 mg/kg, 8 mg/kg, 9 mg/kg, 10 mg/kg, 11 mg/kg, 12 mg/kg, 13 mg/kg, 14 mg/kg, 15 mg/kg, 16 mg/kg, 17 mg/kg, 18 mg/kg, 19 mg/kg or 20 mg/kg which can be administered daily, twice weekly, once weekly, bi-weekly, or monthly. Exemplary fixed dosages of the MASP-2 inhibitory antibody to be delivered intravenously to treat a subject suffering from a MASP-2dependent complément disease or disorder include, e.g., about 10 mg to about 1000 mg, such as about 50 mg to about 750 mg, such as about 100 mg to about 500 mg, such as about 200 mg to about 400 mg, such as about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, or about 400 mg which can be administered daily, twice weekly, once weekly, bi-weekly, or monthly.

In some embodiments, the formulation is diluted into a pharmaceutically acceptable diluent and administered to a subject in need thereof with an initial i.v. loading dose (e.g., about 300 mg to about 750 mg, such as about 400 mg to about 750 mg, such as about 300 mg to about 500 mg, such as about 300 mg to about 400 mg, such as about 300 mg , about 310 mg, about 320 mg, about 330 mg, about 340 mg, about 350 mg, about 360 mg, about 370 mg, about 380 mg, about 390 mg, or about 400 mg), followed by one or more subcutaneous injections of the formulation with a dosage of Img/kg to 5 mg/kg of body weight, or a fixed dosage of about 100 mg to about 400 mg, such as about 100 mg, about 150 mg, about 200 mg, about 250 mg, about 300 mg, about 350 mg, or about 400 mg. For example, an initial i.v. loading dose may be the preferred administration route in particular instances, such as when a patient is in the hospital or in a clinic and suffering from an acute condition (e.g., aHUS) that requires an initial loading dose followed by maintenance dosing with subcutaneous injection of the formulation.

Examples

The invention is further illustrated in the following examples, which should not be construed as further limiting. Ail literature citations herein are expressly incorporated by reference.

EXAMPLE 1

This Example demonstrates that OMS646, a monoclonal antibody targeting human MASP-2, binds to human MASP-2 with high affinity and blocks the lectin pathway complément activity.

Background

A fully human monoclonal antibody targeting human MASP-2 (set forth as SEQ ID NO:1), referred to as “OMS646” was generated as described in WO2012/151481, which is hereby incorporated herein by reference. The OMS646 monoclonal antibody comprises a heavy chain variable région (VH) set forth as SEQ ID NO:2 and a light chain variable région (VL) set forth as SEQ ID NO:3. OMS646 is comprised of variable régions of human origin fused to human IgG4 heavy chain and lambda light chain constant régions and is secreted as a disulfide-linked glycosylated tetramer consisting of two identical heavy chains (having the amino acid sequence set forth as 4) and two identical lambda light chains (having the amino acid sequence set forth as SEQ ID NO:5). The Asparagine residue (N) at position 295 of the heavy chain (SEQ ID NO:4) is glycosylated and is indicated in bold and underlined text.

Heavy Chain Variable Région

Presented below is the heavy-chain variable région (VH) sequence for OMS646. The Kabat CDRs (31-35 (Hl), 50-65 (H2) and 95-107 (H3)) are bolded; and the Chothia CDRs (26-32 (Hl), 52-56 (H2) and 95-101 (H3)) are underlined.

OMS646 heavy chain variable région (VH) (SEQ ID NO:2)

QVTT K FSGPVT .VKPTF.TI.TLTCTVSGFSLSRGKMGVSWIRQPPGKALEWLAHIFSSDEKSYR TSLKSRLTISKDTSKNQVVLTMTNMDPVDTATYYÇARIRRGGIDYWGQGTLVTVSS

Light Chain Variable Région

Presented below is the light-chain variable région (VL) sequence for OMS646. The Kabat CDRs (24-34 (Ll); 50-56 (L2) and 89-97 (L3) are underlined. These régions are the same whether numbered by the Kabat or Chothia System.

OMS646 light chain variable région (VL) (SEQ ID NO:3)

QPVLTQPPSLSVSPGOTASITCSGEKLGDKYAYWYOOKPGOSPVLVMYQDKQRPSGIPERF SGSNSGNTATLTTSGTOAMDEADYYCQAWDSSTAVFGGGTKLTVL

OMS646 heavy chain IgG4 mutated heavy chain full length polypeptide (445 aa) (SEQ ID NO:4)

QVTLKESGPVLVKPTETLTLTCTVSGFSLSRGKMGVSWIRQPPGKALEWLAHIFSSDEKSYRTSLKSRLTISKDT SKNQVVLTMTNMDPVDTATYYCARIRRGGIDYWGQGTLVTVSSASTKGPSVFPLAPCSRSTSESTAALGCLVKDY FPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTKTYTCNVDHKPSNTKVDKRVESKYGPPCP PCPAPEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTYRV VSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTISKAKGQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDI AVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLGK

OMS646 light chain full length polypeptide (212 aa) (SEQ ID NO:5)

QPVLTQPPSLSVSPGQTASITCSGEKLGDKYAYWYQQKPGQSPVLVMYQDKQRPSGIPERFSGSNSGNTATLTIS GTQAMDEADYYCQAWDSSTAVFGGGTKLTVLGQPKAAPSVTLFPPSSEELQANKATLVCLISDFYPGAVTVAWKA DSSPVKAGVETTTPSKQSNNKYAASSYLSLTPEQWKSHRSYSCQVTHEGSTVEKTVAPTECS

As described in WO2012/151481, OMS646 binds to MASP-2 and selectively inhibits the lectin pathway and does not substantially inhibit the classical pathway (i.e., inhibits the lectin pathway while leaving the classical complément pathway intact) and also exhibits at least one or more of the following characteristics: said antibody binds human MASP-2 with a K_D of 10 nM or less, said antibody binds an epitope in the CCP1 domain of MASP-2, said antibody inhibits C3b déposition in an in vitro assay in 1% human sérum at an IC₅₀ of 10 nM or less, said antibody inhibits C3b déposition in 90% human sérum with an IC₅₀ of 30 nM or less, wherein the antibody is an antibody fragment selected from the group consisting of Fv, Fab, Fab', F(ab)₂ and F(ab')₂ wherein the antibody is a single-chain molécule, wherein said antibody is an IgG2 molécule, wherein said antibody is an IgGl molécule, wherein said antibody is an IgG4 molécule, wherein the IgG4 molécule comprises a S228P mutation.

As described in WO2012/151481, OMS646 was determined to avidly bind to human MASP-2 (SEQ ID NO:1) with >5000 fold selectivity when compared to Cls, Clr, MASP-1 or MASP-3. As shown in this example, OMS646 specifïcally binds to human MASP-2 with high affinity and has the ability to block lectin pathway complément activity.

As shown above, OMS646 comprises (a) a heavy-chain variable région comprising (i) CDR-H1 comprising the amino acid sequence from 31-35 of SEQ ID NO:2, ii) CDR-H2 comprising the amino acid sequence from 50-65 of SEQ ID NO:2, and iii) CDR-H3 comprising the amino acid sequence from 95-107 of SEQ ID NO:2; and (b) a light-chain variable région comprising: i) CDR-L1 comprising the amino acid sequence from 24-34 of SEQ ID NO:3, ii) CDR-L2 comprising the amino acid sequence from 50-56 of SEQ ID NO:3, and iii) CDR-L3 comprising the amino acid sequence from 89-97 of SEQ ID NO:3.

As further described in WO2012/151481, a variant of OMS646, having a heavy chain variable région with at least 95% identity to SEQ ID NO:2 and a light chain variable région with at least 95% identity to SEQ ID NO:3 was demonstrated to hâve functional activity similar to OMS646. The OMS646 variant described in WO2012/151481 comprises a) a heavy chain variable région comprising: SEQ ID NO:2, or a variant thereof comprising an amino acid sequence having at least 95% identity to SEQ ID NO:2, wherein residue 31 is an R, residue 32 is a G, residue 33 is a K, residue 34 is an M, residue 35 is a G, residue 36 is a V, residue 37 is an S, residue 50 is an L, residue 51 is an A, residue 52 is an H, residue 53 is an I, residue 54 is an F, residue 55 is an S, residue 56 is an S, residue 57 is a D, residue 58 is an E, residue 59 is a K, residue 60 is an S, residue 61 is a Y, residue 62 is an R, residue 63 is a T, residue 64 is an S, residue 65 is an L, residue 66 is a K, residue 67 is an S, residue 95 is a Y, residue 96 is a Y, residue 97 is a C, residue 98 is an A, residue 99 is an R, residue 100 is an I, residue 101 is an R, residue 102 is an R or A, residue 103 is a G, residue 104 is a G, residue 105 is an I, residue 106 is a D and residue 107 is a Y; and b) a light chain variable région comprising: SEQ ID NO:3 or a variant thereof comprising an amino acid sequence having at least 95% identity to SEQ ID NO:3, wherein residue 23 is an S, residue 24 is a G, residue 25 is an E or D, residue 26 is a K, residue 27 is an L, residue 28 is a G, residue 29 is a D, residue 30 is a K, residue 31 is a Y or F, residue 32 is an A, residue 33 is a Y, residue 49 is a Q, residue 50 is a D, residue 51 is a K or N, residue 52 is a Q or K, residue 53 is an R, residue 54 is a P, residue 55 is an S, residue 56 is a G, residue 88 is a Q, residue 89 is an A, residue 90 is a W, residue 91 is a D, residue 92 is an S, residue 93 is an S, residue 94 is a T, residue 95 is an A, residue 96 is a V and residue 97 is an F.

L QMS646 specifically blocks lectin-dependent activation ofterminal complément components

Methods:

The effect of OMS646 on membrane attack complex (MAC) déposition was analyzed using pathway-specifïc conditions for the lectin pathway, the classical pathway and the alternative pathway. For this purpose, the Wieslab Comp300 complément screening kit (Wieslab, Lund, Sweden) was used following the manufacturer’s instructions.

Results:

FIGURE IA graphically illustrâtes the amount of lectin pathway-dependent MAC déposition in the presence of different amounts of human MASP-2 inhibitory antibody (OMS646). FIGURE IB graphically illustrâtes the amount of classical pathway-dependent MAC déposition in the presence of human MASP-2 inhibitory antibody (OMS 646). FIGURE IC graphically illustrâtes the amount of alternative pathway-dependent MAC déposition in the presence of different amounts of human MASP-2 inhibitory antibody (OMS646). As shown in FIGURE IA, OMS646 blocks lectin pathway-mediated activation of MAC déposition with an IC50 value of approximately 1 nM. However, OMS646 had no effect on MAC déposition generated from classical pathway-mediated activation (FIGURE IB) or from alternative pathway-mediated activation (FIGURE IC).

EXAMPLE 2

OMS646 Pre-Formulation Studies

Background/Rationale:

The composition of a reduced viscosity protein formulation is determined by considération of several factors including, but not limited to: the nature of the protein, the concentration of the protein, the desired pH range, the température at which the protein formulation is to be stored, the period of time over which the protein formulation is to be stored, and how the formulation is to be administered to a patient. For a reduced viscosity formulation to be administered by injection, the protein concentration is dépendent upon the injection volume (usually 1.0 mL to 2.25 mL). If a protein is to be provided at 2 to 4 mg/kg of body weight of a patient, and an average patient weighs 75 kg, then 150 mg-300 mg of the protein will need to be delivered in a 1.0 mL to 1.62 mL injection volume. Viscosity is ideally maintained below about 25 cP to ensure a realistically syringeable subcutaneous therapeutic product. In some embodiments, viscosity is maintained below about 20 cP to allow for delivery of the therapeutic product with an injection device, and also to allow for various types of bioprocessing, such as tangential flow filtration.

The primary aim of these studies was to identify formulation components that would resuit in optimal chemical, physical, and structural stability of OMS646 antibody in liquid formulation resulting in a stable formulation with a viscosity of less than 25 cP, such as less than 20 cP, with a high concentration of OMS646 (100 mg/mL or greater) suitable for subcutaneous injection into a human subject.

Analytic Methods:

To test various buffer and excipient combinations, a purified préparation of OMS646 antibody (102 mg/mL in 20 mM sodium acetate, 50 mg/mL sorbitol, pH 5.0) was diluted to ~ 1 mg/mL in the selected formulation solutions and 4 mL volumes were placed in concentrators pre-rinsed with the appropriate buffer. Each unit was spun down to ~ 1 mL at 3200 x g. This process was repeated for a total of three rounds of buffer-exchange.

Formulation appearance was evaluated using an Eisai Machinery Observation Lamp, Model MIH-DX against water using white and black backgrounds. Each formulation sample was tested for color, clarity (opalescence), and the presence of particulate matter.

The protein content of OMS646 formulations was determined using an extinction coefficient of 1.49 mL/mg*cm. Measurement of absorbance at 280 nm with correction for absorbance at 320 nm was performed using disposable UVettes and a path length of 0.2 cm. Samples were prepared in duplicate by dilution with Ix Dulbecco’s Phosphate-Buffered Saline (DPBS) to a final concentration of ~2 mg/mL. For high concentration samples, the neat solutions were first diluted 1:1 in formulation buffer, and then diluted to ~2 mg/mL in Ix DPBS. Duplicate measurements for each sample were averaged, and the percent relative standard déviation (RSD) was calculated. For any duplicate samples displaying > 5% RSD, an additional dilution set was prepared and measured.

The protein concentration was calculated as follows:

Corrected A280 = A280 - A320

Protein Concentration (mg/mL) = (Corrected A280 * Dilution Factor)/ 1.49 mL/mg*cm

To assess sample turbidity/light scattering, 100 pL of undiluted sample was measured at 320 nm in a disposable UVette using a 1 cm path length. For each sample, the spectrophotometer was blanked with the appropriate buffer-exchange solution without the protein présent. Following measurement, samples were recovered and used for pH analysis. In order to normalize turbidity measurements for sample concentration, A320 was also divided by the concentration in mg/mL and the resulting value in mAU*mL/mg was reported.

pH measurements of ail formulations and solutions were performed at room température using a calibrated SevenMulti Meter (Mettler Toledo) with an automatic température compensation electrode.

The thermal stability of the OMS646 formulations was monitored by differential scanning calorimetry (DSC). Melting température (T_m) data for the mAb were collected using a MicroCal Capillary DSC. The protein samples were diluted to a final concentration of ~2 mg/ml in the appropriate buffer-exchange solution. Evaluation of the samples by DSC was performed by scanning from 20-110°C at l°C/minute or 2°C/minute. The pre-scan thermostat was set to 10 minutes, post-scan thermostat to 0 minutes, and the post-cycle thermostat set to 25°C. For T_m data analysis, a buffer-buffer scan was subtracted from the buffer-sample scan and the thermogram was then normalized to protein concentration (molar) using a molecular weight estimate of 150 kDa. A progressive baseline was generated and subtracted from the data to facilitate Tm détermination. Melting températures were determined using the pick peaks function of the associated Origin® scientific software.

Dynamic light scattering (DLS) measures time-dependent fluctuations in the intensity of scattered light from particles in a sample, where the Stokes Einstein équation is used to calculate the hydrodynamic radius of the particle(s) in solution. The DLS experiments for OMS646 formulations were performed with duplicate undiluted samples (30 - 40 pL) using a DynaPro™ Plate Reader II instrument (Wyatt). A total of 10 individual scans were performed at 25°C, with an acquisition time of 5 seconds. Viscosity was set to that of phosphate buffered saline, 1.019 cP. The résultant intensity distribution plots were compared to evaluate the effects of various formulation components on mean particle size by intensity (overall diameter), a global size distribution width parameter (overall percent polydispersity, or % Pd), the average peak diameter of the OMS646 monomer (Peak 2 diameter), and that peak s width parameter (Peak 2 % Pd). Percent polydispersity (overall or Peak 2) is a width parameter that reflects the heterogeneity detected in the intensity distribution plot, where % Pd < 20% is indicative of a near monodisperse solution and/or species conformation.

Stability against chemical dénaturation was evaluated using the AVIA Isothermal Chemical Dénaturation System (Model 2304), which tests chemical stability under ambient conditions in an automated fashion by generating a dénaturant gradient by mixing constant volumes of formulated protein with formulation buffer and formulation buffer containing urea. Briefly, formulated protein was diluted to 0.33 mg/mL in formulation buffer. For a given formulation, a second formulation buffer containing 10M urea was also prepared. Due to solubility issues, 9M urea solutions were prepared for sucrose- and sorbitol-containing formulations. After a uniform incubation time (~30 minutes), intrinsic protein fluorescence (i.e., tryptophan fluorescence) is measured for each data point, where chemical unfolding of the protein results in exposure of buried tryptophans to solvent with an associated red-shift in the fluorescence signal. For each formulation, data was obtained for a total of 24 urea concentrations (0-9.0M for 10 M urea stocks and 0-8. IM for 9M urea stocks), and the ratio of Abs350/Abs330 was used for baseline subtraction of background fluorescence changes, and a non-linear least squares fit to the unfolding transition data was employed using either a 2state or 3-state model.

Viscosity of the formulations was determined using either a rolling bail viscometer or a rheometer. Ail viscosity measurements were performed at 25°C with a shear rate in the range of 0.5 s'¹ to 1000 s’¹. Rolling bail measurements were performed using an Anton Paar AMVn viscometer. For rolling bail viscosity measurements, the time a gold bail takes to pass a distance in a capillary filled with the sample is measured after tilting the capillary to a predefined angle (80 degrees). Capillaries were tilted a total of three times and the results were averaged to détermine the final dynamic viscosity, a value which is not dépendent on sample density. For rolling bail measurements, the capillary was first cleaned using DI water and methanol. Calibration of the instrument/capillary was confirmed by measurement of 10 cP, 50cP and/or 100 cP Brookfield viscosity standards. The capillary was re-cleaned with DI water and methanol prior to and between every sample measurement.

Rheometer-based viscosity measurements were performed using a DV-III Ultra Programmable Rheometer which was calibrated with Brookfield Viscosity Standard Fluid #10 and #50. 0.5 mL of each sample was measured at various spindle speeds (shear rates). Samples displaying viscosity (cP) readings with <10% RSD for ail shear rates were considered Newtonian over this range, while samples were shear rate-dépendent viscosity were considered non-Newtonian.

Density measurements were carried out using an Anton Paar DMA 4500M Densitometer. Briefly, the instrument was flushed with DI water several times followed by methanoL The instrument was calibrated for air and water prior to measuring the density of water as a sample. The instrument was again washed with water and methanol and a single sample measurement was performed on —175 mg/mL material pooled from several formulations. The reported value was used as a reasonable density approximation for highconcentration OMS646 formulations to be used in gravimétrie content measurements.

Osmolality measurements were performed using a freezing point dépréssion osmometer (Multi-Osmette Osmometer, Précision Systems model 2430), which measures the decrease in a solution’s freezing point as soluté concentration increases.

A liquid particle-counting System (Hach Model 9703, Sensor Model: HRLD-150) was used for determining particle size and abundance in OMS646 formulation samples. Sample data was obtained using a single 500 pL draw of sample (200 pL tare volume). Briefly, the instrument was allowed to warm up for ~30 minutes and both the syringe (1 mL) and System were flushed with deionized water for at least 10 cycles before use. Environment suitability was tested by showing that 25 mL of deionized water contained no more than 25 particles >10 pm in size. System suitability was confirmed by analyzing a single 500 pL draw of 2, 5, 10 and 15 pM standards using appropriate channel sizes. If cumulative counts/mL detected fell within the spécification given for the standard, then the System was deemed suitable for sample testing. Before the first sample measurement, the System was flushed once with Ix Phosphate Buffered Saline (PBS) to ensure that samples did not precipitate upon contact with deionized water. Samples were analyzed using a single 500 pL draw, and cumulative counts/mL for 2 pm, 5 pm, 10 pm and 25 pm channels were determined to the nearest whole number.

Size exclusion chromatography (SEC) was used to evaluate the quantity of aggregates and dégradation products présent in the OMS646 formulations. Briefly, an Agilent 1100 HPLC system was fitted with a G3000SWxl SEC column (Tosoh, 7.8 x 300 mm, 5 pm particle size). OMS646 formulation samples were diluted to 2.5 mg/mL in SEC mobile phase (140 mM potassium phosphate, 75 mM potassium chloride, pH 7.0) and 20 pL of sample was injected into the HPLC column. The system was run using a flow rate of 0.4 mL/min, and eluted protein was detected by absorption at 280 nm (bandwidth 4 nm) with no reference correction. To assess system suitability, ail samples were bracketed by mobile phase blank and gel filtration standard injections, and reference material was injected in duplicate at the beginning of the sequence. Percent abundances for individual and total high molecular weight (HMW) species and low molecular weight (LMW) species, in addition to percent monomer and total integrated peak area were determined.

Analysis by reduced SDS capillary gel (SDS-CE) electrophoresis was performed with a Beckman Coulter PA 800 Plus capillary electrophoresis system and PDA détection module, using an SDS-MW Analysis Kit. Samples and reference were first diluted to LO mg/mL in SDS-MW Sample Buffer. To 95 pL of this working solution 5 pL of β-mercaptoethanol and 2 pL of Internai Standard (10 kDa) were added. Ail samples were centrifuged at 300 x g for 1 minute, heated at 70 ± 2°C for ~10 minutes, and transferred to a PCR vial and kept at 25°C until analysis. Séparations were conducted by applying 15 kV (reverse polarity) across the capillary for 30 minutes and applying a 20.0 psi pressure at both inlet and outlet. Data was acquired at 220 nm with a collection rate of 4 Hz. Reference (unprocessed OMS646) was injected twice at the beginning of each sequence. Percent LC, HC and IgG were reported.

Non-reduced SDS capillary gel electrophoresis analyses were carried out as described for reduced CE-SDS, with the exception that freshly prepared 250 mM iodoacetamide was used in place of reducing agent, and séparations were performed for 35 minutes. Total electropherogram area and % IgG were reported.

A purified préparation of OMS646 antibody (102 mg/mL) was generated using recombinant methods as described in WO2012/151481, which is hereby incorporated herein by reference. Briefly described, OMS646 antibody was generated in CHO cells containing expression constructs encoding the heavy chain and light chain polypeptides of OMS646 and purified using standard techniques.

1. Comparison of Candidate Buffering Systems:

Methods:

In the pre-formulation studies, the stability of MASP-2 inhibitory antibody OMS646 was initially evaluated against a panel of candidate buffers including those commonly used in therapeutic antibody formulation (citrate, histidine, phosphate), as well as more unconventional buffers (acetate, succinate) in order to cover a wide pH range (pH 4.0 - pH 8.0). For this study, the protein was exchanged into 20 mM succinate (pH 4.0, 5.0 and 5.5), acetate (pH 4.0, 5.0 and 5.5), citrate (pH 5.0, 6.0 and 7.0), histidine (pH 6.0 and 7.0) and phosphate (pH 6.0, 7.0 and 8.0) buffers using Amicon Ultra-4 (10 kDa MWCO) concentrators. A purified préparation of OMS646 antibody (102 mg/mL in 20 mM sodium acetate, 50 mg/mL sorbitol, pH 5.0) was diluted to ~1 mg/mL in each of the 14 formulation solutions, and 4.0 mL volumes were placed in concentrators pre-rinsed with the appropriate buffer. Each unit was spun down to ~1 mL at 3200 x g. This process was repeated for a total of three rounds of buffer-exchange. During the final round of concentration, the protein was over-concentrated to < 1 mL. The approximate volume and centrifuge time of each solution was recorded after each cycle.

Results: Overall, the data generated for the five buffer types were comparable with regard to buffer-exchange rate, protein content recovery, differential scanning colorimetry (DSC), dynamic light scattering (DLS) and chemical stability (data not shown). Acetate, citrate and histidine were selected for further évaluation based on the apparent overall optimal thermal and conformational OMS646 properties in the pH range 5.5-6.0. Acetate was selected over succinate at pH 5.5 due primarily to superior thermal stability, while histidine and citrate were selected over phosphate at pH 6.0 based upon DLS data.

2. Excipient Screening

The stability of OMS646 was evaluated in the presence of various excipients with reported antibody-stabilizing properties, using buffering Systems identified during baseline buffer screening (20 mM acetate, pH 5.5; citrate, pH 6.0, and histidine, pH 6.0). For this study, OMS646 was buffer-exchanged into each candidate buffer containing either 150 mM NaCl, 250 mM sorbitol, 250 mM sucrose, 150 mM L-arginine, 150 mM L-glutamate or 250 mM L-proline using Amicon Ultra-4 (10 kDa MWCO) concentrators. Sample préparation was carried out as described in the buffer System comparison wherein the target protein concentration was 2.0 mg/mL.

Results:

With regard to protein recoveries, the estimated protein recoveries ranged from ~72106%, which represented a modest improvement over recoveries in the absence of excipient. Histidine buffer appeared to be preferred for the majority of excipients, and acetate and citrate showed mixed results.

With regard to DSC, it was observed that citrate buffer resulted in OMS646 thermal stabilization for ail excipients tested. FIGURE 2A graphically illustrâtes the results for Dynamic Light Scattering (DLS) analysis for OMS646 formulation excipient screening, showing the overall particle diameter observed for formulations containing various candidate excipients. FIGURE 2B graphically illustrâtes the results for DLS analysis for OMS646 formulation excipient screening, showing the overall polydispersity observed for formulations containing various candidate excipients. As shown in FIGURE 2A and 2B, with regard to DLS, most formulations yielded comparable results. However, for ail buffering Systems, sucrose was associated with elevated polydispersity and the largest overall and monomeric diameters. Following sucrose, sorbitol was the least preferred by DLS, showing larger mean sizes and increased polydispersity. The remaining formulations were generally comparable by DLS with monomer diameters of 10-12 nm (see FIGURE 2A) and polydispersity <20% indicating monodisperse populations (see FIGURE 2B). With regard to stability against chemical dénaturation, as evaluated using the AVIA Isothermal Chemical Dénaturation System, a buffer/pH trend was clearly observed where acetate pH 5.5 formulations denatured at urea concentrations ~0.5 M lower than citrate and histidine pH 6.0 formulations for ail excipients tested. Citrate and histidine were comparable for ail excipients.

In summary, the data supported citrate at approximately a pH of 6.0 as the optimal buffer/pH combination, which was carried forward into solubility screening studies. Given the poor DLS data observed with ail buffer types, sucrose was excluded from further considération.

3. Solubility/Viscosity Screening

First Viscosity Study:

Methods:

In order to establish conditions for maximum OMS646 solubility, 20 mM citrate (pH 5.0 and 6.0) and 20 mM succinate (pH 4.0) were used in the presence of several isotonie combinations of NaCl, sorbitol, arginine, glutamate and proline. OMS646 was bufferexchanged using Amicon 15 concentrator units in multiple cycles and on the final cycle the volume of each solution was reduced to ~1 mL. Buffer exchange rates for ail formulations and exchange cycles were recorded and analyzed. Following buffer exchange, protein contents were measured, percent recovery was calculated and the samples were stored ovemight at 5°C. During storage, the succinate/glutamate formulation was observed to precipitate and was not evaluated further. Remaining formulations were added to Amicon 4 concentrator units and concentrated until a target concentration of-200 mg/mL was reached, or until centrifugation no longer resulted in volume réduction and/or sample viscosity (via sample manipulation) was deemed to be unmanageable.

Results:

With regard to buffer-exchange rates, the highest exchange rates were clearly observed in pH 4.0 samples, with succinate/sorbitol showing the fastest exchange rates overall. Exchange rates at pH 5.0 and 6.0 were comparable, where formations containing only charged amino acid excipients showed higher rates than other formulations. The slowest exchange rate was observed for the citrate/sorbitol formulation at pH 6.0. This formulation was the lone sample with pH > 5.0 and an uncharged excipient component. Under the assumption that exchange rate is a surrogate indicator for OMS646 self-association, it appears that charged species are important for mitigating this behavior at a more neutral pH. With regard to DLS, ail high-concentration formulations showed comparable overall diameters of ~12nm, with the exception of succinate/arginine pH 4.0 which showed an elevated global size distribution at >18 nM.

The buffer-exchanged samples were concentrated until solutions became physically unworkable due to high viscosity. Maximum concentrations in excess of 225 mg/mL were achieved for both pH 4.0 formulations. For formulations at higher pH values, maximal OMS646 protein concentrations ranged from 160.5 to 207.6 mg/mL. Viscosity for the majority of formulations was evaluated using a rolling bail viscometer with a shear rate between 0.5 s'¹ to 1000 s’¹ as described above. FIGURE 3 graphically illustrâtes the results of viscosity analysis for OMS646 solubility screening over a range of protein concentrations in various formulations as measured at pH 5.0 and pH 6.0. As shown in FIGURE 3, when plotted against protein concentration, an exponential increase in viscosity was observed over the formulations, with the highest viscosity recorded for citrate/arginine/glutamate pH 5.0 (161.1 cP for a 196.6 mg/mL solution). At pH 6.0 and a comparable OMS646 protein concentration, the citrate/sorbitol formulation showed considerably higher viscosity than either the sorbitol/glutamate or proline/glutamate formulation. The citrate/arginine/glutamate pH 6.0 formulation (95.3 mg/mL) displayed approximately halfthe viscosity (5.8 vs. 9.3 cP) of the citrate/NaCl pH 6.0 sample (87.5 mg/mL) at a higher protein content suggesting an importance of charged amino acids over ionic excipients.

It is important to note that at a given concentration (i.e., 125 mg/mL), viscosity varies dramatically as a function of the formulation. Viscosity is ideally maintained below ~25 cP to ensure a realistically syringeable subcutaneous therapeutic product. In some embodiments of the OMS646 formulation, viscosity is maintained below about 20 cP to allow for delivery of the therapeutic product with an injection device, and also to allow for various types of bioprocessing, such as tangential flow filtration.

Second Viscosity Study

In an effort to reduce OMS646 formulation viscosity and, thus, maximize OMS646 concentration in a given formulation, an additional study was performed. Based on the initial results, the formulations most likely to produce a reduced viscosity formulation at high concentration were selected, namely: succinate/sorbitol pH 4.0 and glutamate-and argininecontaining citrate formulations at pH 6.0. Based on previous studies, charged amino acids were associated with several bénéficiai properties at neutral pH including increased bufferexchange rate, increased sample processing recovery, and reduced viscosity. The impact of amino acids with a positively charged side chain (e.g., arginine) or amino acids with a negatively charged side chain (e.g., glutamate) were evaluated over a range of concentrations (50 mM to 150 mM) to gauge both excipient charge and concentration on viscosity. Finally, CaCb was used as an additive in both isotonie and hypertonie citrate/glutamate solutions due to its potential viscosity reducing properties as described in U.S. Patent No. 7,390,786.

Samples were buffer-exchanged and concentrated as described above. Following buffer-exchange, the protein content of ail formulations was calculated. The exception was the formulation containing 50 mM glutamate and 50 mM CaCh, which precipitated following buffer-exchange and was not evaluated further. This is likely due in part to the limited solubility of citrate and divalent cations such as Ca²⁺.

Results:

FIGURE 4 graphically illustrâtes the percent protein recovery following bufferexchange for the OMS646 solubility/viscosity study with various candidate formulations. As shown in FIGURE 4, a trend towards increasing recovery with increasing arginine concentration was observed, where the 150 mM arginine formulation showed the highest protein recovery at 85%. Recoveries for the remaining formulations were comparable and ranged from 64-75%. Samples were then concentrated as described above until they became manually unworkable. Ail formulations were evaluated for viscosity as described above and the results are shown below in TABLE 3.

TABLE 3: Summary of the viscosity data from the pre-formulation studies

Sample	Buffer	Excipient	Additive	pH	Cône (mg/mL)	Viscosity (cP)
100 cP Standard (97.2 cP Claim)	-	97.1
50 cP Standard (49.2 Claim)	-	49.1
SI	20 mM Succinate	250 mM sorbitol	-	4.0	209.3	109.6
S2	20 mM Citrate	150 mM Arginine	-	6.0	181.2	70.5
S3	20 mM Citrate	100 mM Arginine	-	6.0	170.8	102.8
S4	20 mM Citrate	50 mM Arginine	-	6.0	158.3	140.1
S5	20 mM Citrate	150mM Glutamate	-	6.0	180.3	71.2
S6	20 mM Citrate	100 mM Glutamate	-	6.0	170.7	74.6
S7	20 mM Citrate	50 mM Glutamate	-	6.0	152.7	137.0
S8	20 mM Citrate	150 mM Glutamate	50 mM CaCl2	6.0	202.8 Ί	73.4

As shown above in TABLE 3, viscosities for ail formulations were >70 cP, and despite the broad range of final concentrations, clear trends were observed. From this 5 preliminary data, it was évident that increased arginine or glutamate concentration led to reduced viscosity. The viscosity of the succinate/sorbitol formulation appeared comparable to the 150 mM amino acid formulations. Inclusion of CaCb showed a réduction in viscosity, where viscosity for this formulation was comparable to samples of 10% lower protein content.

Four formulations (SI, S2, S5 and S8 shown in TABLE 3) were selected for a more detailed viscosity analysis, where recovered neat samples were incrementally diluted in formulation buffer of 25 mg/mL. FIGURE 5 graphically illustrâtes the viscosity (as determined by exponential fit of the viscosity data) versus protein concentration for the OMS646 solubility/viscosity study with various candidate formulations. The exponential fit 15 of the viscosity data was determined in accordance with the methods described in Connolly

B. et al., Biophysical Journal vol 103:69-78, 2012. As shown in FIGURE 5, the 150 mM glutamate and arginine formulations showed almost identical curves that displayed the highest viscosity per unit concentration- a viscosity of 25 cP equating to ~ 150 mg/mL OMS646. The succinate sorbitol formulation performed somewhat better, with 25 cP corresponding to an estimated OMS646 content of -160 mg/mL. The lowest overall viscosity was observed in the CaCb-containing formulation where the estimated content at 25 cP was -175 mg/mL. The most intriguing resuit of this analysis was that the hypertonie formulation including 150 mM glutamate and 50 mM CaCh dramatically reduced sample viscosity. Given the desire for the highest concentration liquid formulation possible, the application of divalent cations and hypertonicity towards viscosity réduction was carried forward into an additional viscosity study.

Third Viscosity Study

Based on the results from the initial viscosity studies described above, an additional study was carried out to détermine whether the apparent viscosity reducing properties of CaCh were related to the divalent Ca²⁺ or hypertonicity. A change in predominate excipient from glutamate to arginine was performed due to the improved buffer-exchange rates observed for arginine-containing formations. The incorporation of histidine was performed due to the potential for chélation of Ca²⁺ by citrate which could lead to précipitation. A subset of samples also evaluated the impact of pH and surfactant on sample viscosity, as well as the impact of CaCh and hypertonicity on the succinate/sorbitol pH 4.0 formulation. Samples were buffer-exchanged and concentrated as described for the previous viscosity studies. Viscosity for ail formulations was measured using a rolling bail instrument as described above. Viscosity data was normalized to a sample protein concentration of 170 mg/mL. This was performed by first calculating a theoretical viscosity from the measured protein content using the exponential régression to previously calculated Viscosity/Solubility viscosity data from the citrate/arginine pH 6.0 formulation (y=0.0917^e00361x). The normalized viscosity was calculated by multiplying the theoretical viscosity for citrate/arginine pH 6.0 at 170 mg/mL (42.4 cP) by measured viscosity/theoretical viscosity (see Table 4, footnote b). The resulting normalized viscosities reveal much clearer trends by smoothing concentration-associated variability (see TABLE 4 and FIGURE 6).

TABLE 4. Summary of Viscosity Data for OMS646 (170 mg/mL) formulations

Form #	Buffer/ PH	Excipient	Additive	PS-80	Viscosity (cP)	Means Norm Cône (mg/mL)	Theor Viscosity (cP)a	Approx Norm Viscosity at 170 mg/mL (cP)b
100 cP Standard (97.2 cP Claim)	96.9	-
IA	20 mM Citrate pH 6.0	112.5 mM Arginine	25 mM CaCh	-	38.8	165.5	36.0	45.7
IB	112.5 mM Arginine	25 mM CaCl2	0.05%	41.7	168.5	40.2	44.0
2	150 mM Arginine	-	-	20.8	155.7	25.3	34.9
3	150 mM Arginine	25 mM CaCl2	-	20.1	157.0	26.5	32.2
4	200 mM Arginine	-	-	22.3	169.1	41.0	23.1
5	225 mM Arginine	-	-	20.2	169.0	40.9	20.9
6A	20 mM Citrate pH 5.0	112.5 mM Arginine	25 mM CaCh	-	34.1	165.4	35.9	40.4
6B	112.5 mM Arginine	25 mM CaCh	0.05%	31.0	170.0	42.4	31.1
7	150 mM Arginine	-	-	22.1	158.9	28.4	33.0
8	150 mM Arginine	25 mM CaCl2	-	17.4	153.9	23.7	31.1
9	20 mM Histidi ne pH 6.0	75 mM Arginine	50 mM CaCl2	-	19.9	174.5	49.9	16.9
10A	112.5 mM Arginine	25 mM CaCh	-	27.9	169.6	41.8	28.4
10B	112.5 mM Arginine	25 mM CaCh	0.05%	28.1	184.6	71.8	16.6
11	135 mM Arginine	10 mM CaCh	-	34.1	167.1	38.2	37.9
12	150 mM Arginine	-	-	35.5	156.6	26.1	57.7
13	200 mM Arginine	-	-	20.2	167.2	38.3	22.3
14	225 mM Arginine	-	-	16.4	161.9	31.6	22.0
15	150 mM Arginine	50 mM CaCh	-	15.9	164.9	35.2	19.1
16A	20 mM Succin ate pH 4.0	125 mM Sorbitol	50 mM CaCl2	-	19.5	172.7	46.7	17.7
16B	125 mM Sorbitol	50 mM CaCh	0.05%	18.1	168.7	40.4	19.0
17	250 mM Sorbitol	50 mM CaCl2	-	15.5	157.2	26.8	24.6
18	250 mM Sorbitol		-	16.8	161.3	31.0	23.0

^aTheoretical viscosity was calculated using the régression to the measured content citrate/arginine pH 6.0 viscosity curve (y=0.0917^e° ^0361x) ^bTheoretical viscosity of 170 mg/mL citrate/arginine pH 6.0 (42.4 cP)* (Measured Viscosity/Theor

Viscosity)

FIGURE 6 graphically illustrâtes the concentration-normalized viscosity data for the viscosity study with various candidate OMS646 formulations based on the data from TABLE 4. As shown in FIGURE 6 and TABLE 4, for citrate and histidine formulations, examination 10 of the normalized data set clearly shows that hypertonicity leads to reduced sample viscosity, wherein the majority of the impact is observed with only modest increases in arginine concentration. For example, the normalized viscosity of formulation 12 (20 mM histidine with 150 mM arginine) is 57.7 cP, compared with viscosities of 22.3 and 22.0 cP for histidine formulations containing 200 and 225 mM arginine, respectively. A similar trend was observed for citrate/arginine formulations. There was no obvious benefit of CaCh inclusion. Rather, it was surprising to fmd that in the absence of CaCh, low viscosities (e.g., less than 25 cP) were achieved with the citrate/arginine and the histidine/arginine formulations with an arginine concentration of 200 mM or greater. Inclusion of 0.05% PS-80 resulted in substantial viscosity réduction in two of the three formulations evaluated at pH > 5.0. Finally, viscosities at pH 5.0 appeared somewhat lower than those for comparable formulations at pH 6.0.

In view of the results obtained from the viscosity studies, hypertonie arginine, the presence or absence of divalent cations and the succinate/sorbitol pH 4.0 formulations were carried forward into surfactant screening studies to further evaluate the impact on OMS646 physical, conformation, and chemical stability.

4. Surfactant Screening

The impact of surfactant on OMS646 stability was evaluated using candidate formulations identified in prior studies described herein. For surfactant screening studies, six formulations were analyzed as follows:

mM citrate, 200 mM arginine at pH 5.0 mM citrate, 200 mM arginine at pH 6.0;

mM succinate, 250 mM sorbitol at pH 4.0;

mM histidine, 200 mM arginine at pH 6.0;

mM histidine, 75 mM arginine/50 mM CaCh at pH 6.0;

mM histidine, 75 mM arginine/50 mM MgCh at pH 6.0

Each of the six formulations shown above was evaluated either without surfactant or in the presence of 0.01% PS-80 for a total of twelve unique formulation conditions. For each formulation, OMS646 was exchanged into buffer-exchange solutions (no PS-80), concentrated, the content was measured and the samples were normalized to 175 mg/mL protein. Each formulation was then split and PS-80 was added into the appropriate samples to a final concentration of 0.01% (w/v).

The formulated samples were each subjected to mechanical stress by agitation, and freeze/thaw cycling. For both types of stress, 0.5 mL of sample was transferred into four type borosilicate glass vials (2.0 mL) and sealed using FluroTec® stoppers. For agitation stress, the samples were placed in a microplate shaker at 600 rpm for ~60 hours at room température. Agitation control samples were kept next to the shaker for the duration of the agitation stress. For freeze/thaw cycling, the samples were frozen at -80°C for >60 minutes and then allowed to thaw at room température, for a total of 5 freeze-thaw cycles. Following stressing, samples were stored at 2-8°C until analysis. The remaining sample was maintained at 2-8°C as an unstressed control. Appearance, A280 measurements, DLS and SEC were performed to evaluate the impact of surfactant on OMS646 aggregation and stability.

Results:

Following stressing of the six OMS646 formulations, no sample showed evidence of product-related particulate matter. Protein content was essentially constant for ail samples of a given formulation. Analysis of DLS data for freeze/thaw and agitation samples revealed only subtle différences between formulations and stress-types, with no clear global trends observed with regard to PS-80 inclusion. The one exception was the succinate/sorbitol pH 4.0 formulation in which inclusion of PS-80 led to high overall polydispersity (i.e., multimodal) for freeze/thaw and 5°C control samples. This acidic formulation also showed evidence of aggregation/self-association by DLS in the absence of PS-80 upon agitation.

Analysis of SEC data was performed to evaluate any aggregation and/or dégradation products arising during sample stressing. The results are summarized in TABLES 5A-5D.

TABLE 5A: Summary of SEC data for OMS646 formulation surfactant screening (2-8°C)

Form.	Buffer	Excipient	Additive	PH	PS- 80 (%)	Ave Total HMW (%)	Ave Monomer (%)	Ave Total LMW (%)
Average Unprocessed Reference Sample	3.7	96.3	-
1	20 mM citrate	200 mM Arginine	-	5.0	-	3.0	96.3	-
2			0.01	3.1	96.9	-
3	20 mM citrate	200 mM Arginine	-	6.0	-	3.2	96.8	-
4			0.01	3.3	96.7	-
5	20 mM histidine	200 mM Arginine	-	6.0	-	3.3	96.7	-
6			0.01	3.4	96.6	-
7	20 mM Succinate	250 mM Sorbitol	-	4.0	-	3.2	96.6	0.2
8			0.01	3.2	96.5	0.2
9	20 mM histidine	75 mM Arginine	50 mM CaCl2	6.0	-	3.3	96.7	-
10		0.01	3.4	96.6	-
11	20 mM histidine	75 mM Arginine	50 mM	6.0	-	3.4	96.6	-
12	MgCl2		0.01	3.5	96.5	-

TABLE 5B: Summary of SEC data for OMS646 formulation surfactant screening (Freeze/Thaw)

Form.	Buffer	Excipient	Additive	PH	PS-80 (%)	Ave Total HMW (%)	Ave Monomer (%)	Ave Total LMW (%)
Average Unprocessed Reference Sample	3.7	96.3	-
1	20 mM citrate	200 mM Arginine	-	5.0	-	3.1	96.9	-
2			0.01	3.2	96.8	-
3	20 mM citrate	200 mM Arginine	-	6.0	-	3.3	96.7	-
4			0.01	3.3	96.7	-
5	20 mM histidine	200 mM Arginine	-	6.0	-	3.3	96.7	-
6			0.01	3.4	96.6	-
7	20 mM Succinate	250 mM Sorbitol	-	4.0	-	3.2	96.6	0.2
8			0.01	3.2	96.6	0.2
9	20 mM histidine	75 mM Arginine	50 mM CaCl2	6.0	-	3.4	96.6	-
10		0.01	3.4	96.6	-
11	20 mM	75 mM Arginine	50 mM	6.0	-	3.5	96.6	-
12	histidine	MgCl2		0.01	3.5	96.6	-

TABLE 5C: Summary of SEC data for OMS646 formulation surfactant screening (25°C)

Form.	Buffer	Excipient	Additive	pH	PS- 80 (%)	Ave Total HMW (%)	Ave Monome r (%)	Ave Total LMW (%)
Average Unprocessed Reference Sample	3.7	96.3	-
l	20 mM citrate	200 mM Arginine	-	5.0	-	3.1	96.9	-
2			0.01	3.2	96.8	-
3	20 mM citrate	200 mM Arginine	-	6.0	-	3.3	96.7	-
4			0.01	3.4	96.6	-
5	20 mM histidine	200 mM Arginine	-	6.0	-	3.3	96.7	-
6			0.01	3.4	96.6	-
7	20 mM Succinate	250 mM Sorbitol	-	4.0	-	3.3	96.5	0.2
8			0.01	3.3	96.5	0.2
9	20 mM histidine	75 mM Arginine	50 mM CaCl2	6.0	-	3.4	96.6	-
10		0.01	3.5	96.5	-
11	20 mM histidine	75 mM Arginine	50 mM	6.0	-	3.5	96.5	-
12	MgCl2		0.01	3.5	96.5	-

TABLE 5D: Summary of SEC data for OMS646 formulation surfactant screening (Agitation)

Form.	Buffer	Excipient	Additive	PH	PS- 80 (%)	Ave Total HMW (%)	Ave Monome r (%)	Ave Total LMW (%)
Average Unprocessed Reference Sample	3.7	96.3	-
1	20 mM citrate	200 mM Arginine	-	5.0	-	3.0	97.0	-
2			0.01	3.2	96.8	-
3	20 mM citrate	200 mM Arginine	-	6.0	-	3.3	96.7	-
4			0.01	3.4	96.6	-
5	20 mM histidine	200 mM Arginine	-	6.0	-	3.3	96.7	-
6			0.01	3.4	96.6	-
7	20 mM Succinate	250 mM Sorbitol	-	4.0	-	2.8	97.0	0.2
8			0.01	3.3	96.5	0.2
9	20 mM histidine	75 mM Arginine	50 mM CaCh	6.0	-	3.4	96.3	0.3
10		0.01	3.5	96.5	-
11	20 mM histidine	75 mM Arginine	50 mM	6.0	-	3.4	96.6	-
12	MgCl2		0.01	3.6	96.5	-

As shown above in TABLES 5A-5D, overall, the SEC data indicate that the OMS646 molécule is generally insensitive to inclusion of PS-80 and both freeze/thaw (TABLE 5B) and agitation stress (TABLE 5D), regardless of surfactant. It was observed that the worst performing OMS646 formulations were those containing divalent cation additives (CaCh and MgCh) where high molecular weight (HMW) material for these samples was clearly elevated relative to other samples and the lowest levels of monomer were observed.

5. Stability analysis under stressed and unstressed conditions for 28 days

After narrowing the potential buffer, excipient, and surfactant combinations through the pre-formulation studies described above, citrate and histidine buffers were formulated using 200 mM arginine over the pH range 5.5 - 6.5 at high concentrations of 175 mg/mL and 200 mg/mL OMS646 to identify the most suitable formulation under both stressed (40°C) and unstressed (5°C) conditions. Arginine was included at a hypertonie level (200 mM) due to the viscosity-reducing properties at this elevated concentration. Based on statistical numerical optimization of the pre-formulation data, the most suitable OMS646 formulation was determined to be 20 mM citrate and 200 mM arginine. A panel of samples was also prepared to evaluate the impact of 0.01% PS-80 on citrate and histidine formulations.

Buffer-exchange was carried out as described above, samples were concentrated and diluted to achieve the target concentrations of 175 or 200 mg/mL OMS646. During this final normalization, PS-80 was added to 0.01% for the appropriate formulations. The formulations were stérile filtered using Millipore Ultrafree-CL GV 0.22 μΜ stérile concentrators. One vial of each formulation was placed at 5°C and one at 40°C for a 28 day incubation period. The samples were analyzed at To and 28 days with regard to concentration, appearance, turbidity, osmolality, pH, DLS, DSC and viscosity. Following the 28 day incubation, it was observed that both the 175 and 200 mg/mL OMS646 succinate/sorbitol formulation stored at 40°C developed a gel-like consistency, and thus were not analyzed.

Results:

With regard to the stability analysis, pH values remained stable over the duration of the study, regardless of formulation and storage condition. After 28 days, both SEC and SDS-CE analysis indicated substantial increases in LMW content for the acidic pH 5.0 and pH 4.0 formulations, eliminating these formulations from further considération. For the pH 6.0 citrate/arginine and histidine/arginine formulated with 0.01% PS-80, most responses were nearly indistinguishable from associated surfactant-free samples. SEC, however, showed réductions in HMW content of 0.2% - 0.6% relative to surfactant-free counterpart formulations. Coupled with the apparent viscosity-reducing properties of the surfactant, polysorbate-80 (PS-80) was chosen to be included in further formulation studies.

The concentration and viscosities of a total of 10 formulations were tested after 28 days at 5°C. Représentative results are shown in TABLE 6.

TABLE 6. Viscosity of Formulations after 28 days at 5°C.

Sample	Formulation	Concentration 28 days at 5°C (mg/mL)	Viscosity (cP)
1	20 mM Citrate, 200 mM Arginine, pH 6.0, 175 mg/mL OMS646	153.4	10.6
2	20 mM Histidine, 200 mM Arginine, pH 6.0, 175 mg/mL OMS646	151.3	12.7
3	20 mM Citrate, 200 mM Arginine, pH 6.0, 200 mg/mL OMS646	170.5	27.4
4	20 mM Histidine, 200 mM Arginine, pH 6.0, 200 mg/mL OMS646	184.2	18.1
5	20 mM Citrate, 200 mM Arginine, 0.01% PS-80, pH 6.0, 175 mg/mL OMS646	159.2	9.0
6	20 mM Histidine, 200 mM Arginine, 0.01% PS-80, pH 6.0, 175 mg/mL OMS646	156.0	7.8
7	20 mM Citrate, 200 mM Arginine, pH 5.0, 175 mg/mL OMS646	143.2	9.8
8	20 mM Histidine, 200 mM Arginine, pH 5.0, 200 mg/mL OMS646	182.4	15.9
9	20 mM Succinate, 250 mM Sorbitol, pH 4.0, 175 mg/mL OMS646	150.6	14.5
10	20 mM Succinate, 250 mM Sorbitol, pH 4.0, 200 mg/mL	184.3	18.0

As shown above in TABLE 6, higher concentration formulations displayed higher viscosities. Of considérable interest was the observation that inclusion of PS-80 led to réduction in viscosity for both citrate (10.6 vs 9.0 cP) and histidine (12.7 vs. 7.8 cP) formulations, while also preserving protein recovery. Such réductions in viscosity upon inclusion of PS-80 are bénéficiai, allowing for a higher concentration of OMS646 while maintaining a low viscosity that is considered to be syringeable in a clinical setting and also suitable for use in an autoinjector and other injection devices.

Summary of the results

The primary aim of these studies was to identify formulation components that would resuit in optimal chemical, physical, and structural stability of high concentration OMS646 antibody in liquid formulations. In addition, several viscosity-specific studies were carried with the goal of obtaining a final formulation with maximal OMS646 antibody concentration that could be feasibly delivered by subcutaneous administration.

Several buffer types, pH conditions, excipients, and surfactant concentrations were evaluated in an itérative fashion over the course of the studies directed at évaluation of buffer Systems, excipients, solubility, viscosity, and surfactant screening studies. The initial

Baseline Buffer Evaluation Study tested five different buffer types (acetate, citrate, succinate, histidine, and phosphate) over the pH range 4.0 - 8.0. Analysis by DSC, DLS, and the AVIA chemical dénaturation System indicated that more acidic and basic conditions were least suitable for OMS646 antibody stability. Based on the results, acetate, citrate, and histidine buffer Systems were selected for further évaluation.

Excipient screening evaluated the effect of NaCl, L-arginine, L-glutamate, L-proline, sucrose, and sorbitol on OMS646 antibody stability in each of the three chosen buffer Systems. Citrate (pH 6.0) was carried forward alone into further studies to maximize design space for additional excipient évaluation. Only sucrose was eliminated as a potential excipient due to poor light scattering data. Solubility screening evaluated the ability of citrate (pH 5.0 and pH 6.0) formulations containing isotonie combinations of NaCl, sorbitol, arginine, glutamate, and proline to support high solution concentrations of OMS646 antibody. Ail formulations were concentrated in excess of 150 mg/mL OMS646 without evidence of aggregation. Succinate/arginine and succinate/glutamate formulations, however, showed evidence of precipitation/aggregation following short-term storage and were not evaluated further. Biophysical analysis of the citrate formulations showed only minor différences between excipients at pH 6.0 and only a modest réduction of HMW content in counterpart pH 5.0 formulations.

Interesting data came from viscosity measurements of this subset of samples, which suggested that citrate/glutamate and succinate/sorbitol imparted the lowest viscosities. Given the similar biophysical stabilities observed between excipients and the importance of obtaining a formulation with maximum OMS646 content, additional viscosity studies were performed. These viscosity studies identified divalent cations and/or modest hypertonicity as a significant factor in reducing OMS646 antibody formulation viscosity at more neutral pH. Both citrate (pH 5.0 and 6.0) and histidine (pH 6.0) were evaluated in the presence of 200 mM arginine. Histidine pH 6.0 was also evaluated in the presence of 75 mM arginine and either 50 mM CaCh or 50 mM MgCL. Finally, succinate/sorbitol pH 4.0 was tested. Ail buffer/excipient combinations were tested either in the absence or presence of 0.01% PS-80 to détermine if surfactant promoted OMS646 antibody stability under agitation and freeze/thaw stress conditions. Ail formulations appeared stable against the environmental stresses applied, regardless of surfactant. One striking observation was the increase in OMS646 HMW content observed by SEC for formulations containing divalent cations. Therefore, CaCL and MgCL were eliminated form further considération as excipients. Succinate/sorbitol also showed reduced OMS646 antibody purity, which was mainly attributable to an apparent increase in LMW impurities. While the différences between formulation containing and lacking 0.01% PS-80 were minor, samples containing surfactant did appear to show modestly increased HMW content (-0.1%) relative to their surfactant-free counterparts.

EXAMPLE 3

This Example describes a study in which three candidate highly concentrated, low viscosity OMS646 formulations, identified based on the pre-formulation studies described in Example 2, were compared with respect to syringeability.

Background/Rationale:

The time and force required for a manual injection (or time required for an injection using an auto-injector) are important and may impact the ease of use of the product by the end-user and thus compliance. The force required for the injection of a solution at a given injection rate via a needle of predetermined gauge and length is referred to as ‘syringeability’ (see e.g., Burckhuchler, V.; et al., Eur. J. Pharm. Biopharm. 76 (3), 351-356, 2010). With regard to syringeability for administration to a human subject, one generally does not want to exceed a 25N force (although there are marketed formulations more viscous than this). A 27GA needle or a 27GA thin wall needle are generally considered standard needles for subcutaneous injection of monoclonal antibodies. The 27GA thin wall needle has an ID roughly equal to a 25GA needle (smaller G numbers are bigger diameters).

The following study was carried out to détermine the syringeability of three candidate highly concentration low viscosity OMS646 formulations.

Methods:

Based on the pre-formulation studies described in Example 2, the following three candidate high concentration OMS646 formulations were selected and further studied, as shown in TABLE 7. In this example, the formulations were prepared using arginine hydrochloride, polysorbate 80 if indicated, and either trisodium citrate or histidine, with the pH being adjusted to about 5.8 to 6.0 using hydrochloric acid.

TABLE 7: Candidate high concentration OMS646 formulations

Formulation	Buffer/Excipients/Surfactant/pH	Concentration of OMS646	Protein content
1	20 mM Citrate, 200 mM Arginine, 0.01% PS-80, pH 5.8	185 mg/mL	187.1
2	20 mM Histidine, 200 mM Arginine, 0.01% PS-80, pH5,9	185 mg/mL	188.2
3	20 mM Citrate, 200 mM Arginine, pH 5.8	185 mg/mL	193.3

1. Osmolality and Viscosity of OMS646 candidate formulations

Osmolality and viscosity of the three candidate formulations generated as shown in

TABLE 7 were determined using methods described in Example 2. Fluid behavior of the formulation was considered to be non-Newtonian if the %RSD >10 over shear rates tested. The results are shown in TABLE 8.

TABLE 8. Osmolality and Viscosity

Formulation	Buffer/Excipients/Surfactant/pH	Conc.	Osmolality (mOsm/kg)	Viscosity (cP)	Fluid Behavior
1	20 mM Citrate, 200 mM Arginine, 0.01% PS-80, pH5.8	185 mg/mL	473	16.1	Newtonian
2	20 mM Histidine, 200 mM Arginine, 0.01% PS-80, pH5.9	185 mg/mL	440	15.9	Newtonian
3	20 mM Citrate, 200 mM Arginine, pH5.8	185 mg/mL	468	21.3	Newtonian

2. Syringeability of OMS646 candidate formulations

Methods:

Syringeability analysis of the three OMS646 formulations was carried out with respect to average load and max load using 27 GA (1.25”), 25GA (1”) and 25GA thin-walled (1”) needles. Triplicate replicates of each formulation were each injected once. Results for 15 the syringeability samples are averages of the triple replicates.

Results:

The three formulations shown in TABLE 7 (containing OMS646 at 185 mg/mL) were evaluated for their syringeability using 27GA (1.25”), 25GA thin-walled (1”), and 25GA (1”) needles. Reported results are the average of triplicate replicates. The results are shown in TABLE 9 and are graphically illustrated in FIGURE 7A and 7B. FIGURE 7A graphically illustrâtes the average load (Ibf) of three candidate OMS646 formulations using 27GA, 25GA and 25GA thin-walled needles. FIGURE 7B graphically illustrâtes the maximum load (Ibf) of three candidate OMS646 formulations using 27GA, 25GA and 25GA thin-walled needles.

TABLE 9. Syringeability of the candidate high-concentration OMS646 formulations

Formulation	Condition	Average Load (Ibf)	Max Load (Ibf)	Average Load (N)	Max Load (N)
1	27 GA	4.72	5.07	20.99	22.55
25GA	1.88	2.03	8.36	9.03
25GA (thin-wall)	1.27	1.36	5.65	6.05
2	27 GA	4.51	4.85	20.06	21.57
25GA	1.84	1.99	8.18	8.85
25GA (thin-wall)	1.26	1.32	5.60	5.80
3	27 GA	5.58	5.83	24.82	25.93
25GA	2.29	2.51	10.18	11.16
25GA (thin-wall)	1.50	1.60	6.67	7.11

As described above, with regard to syringeability for administration to a human subject, one generally does not want to exceed a 25N force. As shown above in TABLE 9, ail three candidate high concentration OMS646 formulations hâve acceptable syringeability (i.e., a force not exceeding 25N) when injected through a 25GA or 25GA thin-walled syringe. Formulation #2 also has acceptable syringeability when injected through a 27G needle. The addition of PS-80 0.01% caused an unexpected improvement in syringeability.

3. SEC Analysis of OMS646 candidate formulations post-injection

Size exclusion chromatography (SEC) was used to evaluate the quantity of aggregates and dégradation products présent in the three OMS646 candidate formulations post-injection. Briefly, an Agilent 1100 HPLC System was fitted with a G3000SWxl SEC column (Tosoh, 7.8 x 300 mm, 5 pm particle size). OMS646 samples were diluted to 2.5 mg/mL in SEC mobile phase (140 mM potassium phosphate, 75 mM potassium chloride, pH 7.0) and 20 pL of sample was injected into the HPLC column. The System was run using a flow rate of 0.4 mL/min, and eluted protein was detected by absorption at 280 nm (bandwidth 4 nm) with no référencé correction. To assess System suitability, ail samples were bracketed by mobile phase blank and gel filtration standard injections, and référencé material was injected in duplicate at the beginning of the sequence. Percent abundances for individual and total high molecular weight (HMW) species and low molecular weight (LMW) species, in addition to percent monomer and total integrated peak area were reported.

Results:

The results of the SEC analysis of the high concentration OMS646 candidate formulations post-injection are shown in TABLE 10.

TABLE 10. SEC Analysis of the high-concentration OMS646 formulations post-injection

Formulation	Condition	% Purity	% HMW	% LMW
1	Control	96.5	3.3	0.1
27 GA	96.4	3.5	0.2
25 GA	96.4	3.4	0.2
25 GA (thin-wall)	96.4	3.4	0.2
2	Control	96.6	3.4	Not detected
27 GA	96.5	3.5	Not detected
25 GA	96.5	3.5	Not detected
25 GA (thin-wall)	96.5	3.5	Not detected
3	Control	96.5	3.4	0.2
27 GA	96.3	3.5	0.2
25 GA	96.4	3.5	0.2
25 GA (thin-wall)	96.3	3.5	0.2

These results show little or no change in purity by SEC following expulsion through the needle.

Summary of Results: The results of the syringeability analysis demonstrate that ail three candidate high concentration OMS646 formulations hâve acceptable syringeability when tested using needles suitable for subcutaneous administration and there is little or no change in purity of the OMS646 following expulsion through the needle. The addition of PS80 0.01% provided an unexpected improvement in the syringeability of the citrate argininecontaining formulation.

EXAMPLE 4

This Example describes a study that was carried out to evaluate the stability of candidate high-concentration low viscosity OMS646 antibody formulations during long-term storage.

Methods:

This study was carried out to evaluate the stability of high-concentration OMS646 antibody formulations for subcutaneous injection after long-term storage.

Two candidate formulations were evaluated as follows:

A) 20 mM citrate, 200 mM arginine, 0.01% PS-80, pH 5.8 (185 mg/mL OMS646)

B) 20 mM histidine, 200 mM arginine, 0.01% PS-80, pH 5.9 (185 mg/mL OMS646)

Samples were filled into 13mm, 2mL size USP Type I Schott Glass Tubing Vials (West Pharmaceuticals), with a LOmL sample fill, sealed with 13mm Fluorotec stoppers (West Pharmaceuticals), and capped with 13FO aluminum caps with buttons (West Pharmaceuticals or équivalent). The sample vials were stored in controlled température reach-in stability chambers at -75 ± 10°C, -20 ± 5°C, 5 ± 3°C, 25 ± 2°C/60 ± 5% RH, and 40 ± 2°C/75 ± 5%RH. A target of at least 40 sample vials per formulation were stored for the présent study. Samples stored as liquid were stored in an inverted orientation, while frozen samples were stored upright. The required number of vials was pulled at the associated time points and conditions, and the samples were characterized by the following methods: Appearance by Visual Inspection, Protein Content by A280, Osmolality, SEC-HPLC, pH, and MASP-2 ELISA. The exemplary SEC-HPLC data is summarized in TABLE 11 and shows that the OMS646 antibody maintained its integrity after storage at 5°C for 6, 9 and 12 months. The ELISA data confirmed that the antibody preserved its functionality after storage at 5°C for 6, 9 and 12 months.

Results: The results of this study are summarized in TABLE 11 below.

TABLE 11. Stability of Formulations as analyzed by SEC

Formulation	Time Point	Condition	Total HMW (oligomer) (%)	Main Peak (monomer) (%)	Total LMW (%)
185 mg/mL OMS646 20 mM Citrate 200mM Arginine 0.01% Polysorbate 80 pH 5.8	T0	NA	3.9	96.1	-
1 month	-20°C	2.5	97.5	-
5°C	2.6	97.4	-
25°C/60% RH	2.7	97.3	-
2 months	-20°C	2.9	97.1	-
5°C	3.1	96.9	-
25°C/60% RH	3.4	96.6	-
3 months	-20°C	2.8	97.2.	-
5°C	2.9	97.1	-
25°C/60% RH	3.3	96.0	0.7
6 months	-20°C	1.7	98.3	-
5°C	1.9	98.1	-
25°C/60% RH	2.0	98.0	-
9 months	5°C	3.4	96.6	-
25°C/60% RH	4.0	95.7	0.2
12 months	5°C	3.4	96.6	-
185 mg/mL OMS646 20 mM Histidine 200mM Arginine 0.01% Polysorbate 80 pH5.9	T0	NA	3.8	96.2	-
1 month	-20°C	2.7	97.3	-
5°C	2.7	97.3	-
25°C/60% RH	2.9	97.1	-
2 months	-20°C	2.9	97.1	-
5°C	3.3	96.7	-
25°C/60% RH	3.3	96.7	-
3 months	-20°C	2.8	97.1	0.1
5°C	3.0	96.9	0.1
25°C/60% RH	3.1	96.1	0.8
6 months	-20°C	1.8	98.2	-
5°C	1.9	98.1	-
25°C/60% RH	2.0	98.0	-

As shown in TABLE 11, little or no change in purity was observed in the samples stored up to 9 months at -20°C or stored at 5°C up to 12 months, the intended storage 5 température. The purity of the samples stored at 25°C was also maintained over 2 months, however, slight changes in purity ai 25°C were observed over 9 months of storage.

EXAMPLE 5

An exemplary formulation containing the MASP-2 inhibitory antibody OMS646 at pH 5.8 was prepared by combining OMS646 (185 mg/mL) with citrate (20 mM), arginine (200 mM) and polysorbate 80 (0.01%). Sodium citrate dihydrate (4.89 mg/mL) and citric acid monohydrate (0.71 mg/mL) were used to préparé the citrate buffer, with hydrochloric acid and/or sodium hydroxide used to adjust the pH as needed.

The viscosity of this formulation was measured with a capillary viscometer, and the results are shown in TABLE 12. There is a slight decrease in viscosity at higher shear rates, with ail values being below 13 cP.

TABLE 12: Viscosity of an exemplary OMS646 formulation measured at different shear rates

Formulation	Température (°C)	Shear Rate (1/s)	Viscosity (cP)
185 mg/mL OMS646 20 mM Citrate 200mM Arginine 0.01% Polysorbate 80 pH 5.8	25.0	103000	12.2
25.0	156000	11.5
25.0	211000	11.0

It was determined that dosing human subjects with the exemplary 185 mg/mL OMS646 formulation described in this example (both by subcutaneous injection and intravenous administration after dilution) resulted in sustained and high degrees of lectin pathway inhibition.

While the preferred embodiment of the invention has been illustrated and described, it will be appreciated that various changes to the disclosed formulations and methods can be made therein without departing from the spirit and scope of the invention. It is therefore intended that the scope of letters patent granted hereon be limited only by the définitions of the appended daims.

In accordance with the foregoing, the invention features the following embodiments.

1. A stable pharmaceutical formulation suitable for parentéral administration to a mammalian subject, comprising:

(a) an aqueous solution comprising a buffer System having a pH of 5.0 to 7.0; and (b) a monoclonal antibody or fragment thereof that specifically binds to human MASP-2 at a concentration of about 50 mg/mL to about 250 mg/mL, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising CDR-Hl, CDRH2 and CDR-H3 of SEQ ID NO:2 and (ii) a light chain variable région comprising CDR-L1, CDR-L2 and CDR-L3 of SEQ ID NO:3, or a variant thereof comprising a heavy chain variable région having at least 95% identity to SEQ ID NO:2 and a light chain variable région having at least 95% identity to SEQ ID NO:3;

wherein the formulation has a viscosity of between 2 and 50 centipoise (cP), and wherein the formulation is stable when stored at between 2°C and 8°C for at least one month.

2. The pharmaceutical formulation of paragraph l, wherein the concentration of the antibody in the formulation is from about 100 mg/mL to about 225 mg/mL.

3. The pharmaceutical formulation of paragraph 1, wherein the concentration of the antibody in the formulation is from about 150 mg/mL to about 200 mg/mL.

4. The pharmaceutical formulation of paragraph 1, wherein the concentration of the antibody in the formulation is from about or about 175 mg/mL to about 195 mg/mL.

5. The pharmaceutical formulation of paragraph 1 or paragraph 2, wherein the viscosity of the formulation is from about 2 cP to about 40 cP.

6. The pharmaceutical formulation of paragraph 1 or paragraph 2, wherein the viscosity of the formulation is from about 2 cP to about 30 cP.

7. The pharmaceutical formulation of paragraph 1 or paragraph 2, wherein the viscosity of the formulation is from about 2 cP to about 25 cP.

8. The pharmaceutical formulation of paragraph 1 or paragraph 2, wherein the viscosity of the formulation is from about 2 cP to about 20 cP.

9. The pharmaceutical formulation of paragraph 1 or paragraph 2, wherein the viscosity of the formulation is from about 2 cP to about 18 cP.

10. The pharmaceutical formulation of any one of paragraphe 1-9, wherein the buffer System comprises at least one pharmaceutically acceptable buffering agent having an acid dissociation constant within 2 pH units of the formulation pH.

11. The pharmaceutical formulation of any one of paragraphe 1-10, wherein the buffer System comprises at least one buffering agent selected from the group consisting of succinate, histidine and citrate.

12. The pharmaceutical formulation of paragraph 11, wherein the at least one buffering agent is histidine or citrate.

13. The pharmaceutical formulation of any one of paragraphe 1-12, wherein the at least one buffering agent is citrate.

14. The pharmaceutical formulation of paragraph 13, wherein the at least one buffering agent is sodium citrate.

15. The pharmaceutical formulation of any one of paragraphe 1-12, wherein the at least one buffering agent is histidine.

16. The pharmaceutical formulation of paragraph 15, wherein the at least one buffering agent is L-histidine.

17. The pharmaceutical formulation of paragraph 13, wherein citrate is présent in the solution at a concentration of 10 mM to 50 mM.

18. The pharmaceutical formulation of paragraph 15, wherein histidine is présent in the solution at a concentration of 10 mM to 50 mM.

19. The pharmaceutical formulation of any one of paragraphe 1-18, wherein the pharmaceutical formulation further comprises at least one excipient selected from the group consisting of a protein, an amino acid, a sugar, a polyol, a sait, a fatty acid and a phospholipid.

20. The pharmaceutical formulation of paragraph 19, wherein the at least one excipient is a tonicity modifying agent in a sufficient amount for the formulation to be hypertonie.

21. The pharmaceutical formulation of paragraph 20, wherein the tonicity modifying agent selected from the group consisting of an amino acid with a charged side chain, a sugar or other polyol and a sait.

22. The pharmaceutical formulation of paragraph 21, wherein the tonicity modifying agent is a sugar or other polyol and is selected from the group consisting of sucrose, trehalose, mannitol and sorbitol.

23. The pharmaceutical formulation of paragraph 21, wherein the tonicity modifying agent is a sait selected from the group consisting of NaCI or a sait of an amino acid.

24. The pharmaceutical formulation of paragraph 21, wherein the tonicity modifying agent is an amino acid with a charged side chain.

25. The pharmaceutical formulation of paragraph 24, wherein the amino acid with a charged side chain is présent in the formulation at a concentration of from about 150 mM to about 300 mM.

26. The pharmaceutical formulation of paragraph 24 or 25, wherein the tonicity modifying agent is an amino acid with a negatively charged side chain.

27. The pharmaceutical formulation of paragraph 24 or 25, wherein the tonicity modifying agent excipient is an amino acid with a positively charged side chain.

28. The pharmaceutical formulation of paragraph 26, wherein the tonicity modifying agent is glutamate.

29. The pharmaceutical formulation of paragraph 27, wherein the tonicity modifying agent is arginine.

30. The pharmaceutical formulation of paragraph 29, wherein the tonicity agent is L-arginine HCl.

31. The pharmaceutical formulation of paragraph 29, wherein arginine is présent in the solution at a hypertonie level of from 200 mM to 300 mM.

32. The pharmaceutical formulation of paragraph 17, wherein the solution comprises about 20 mM citrate and has a pH from about 5.5 to about 6.5.

33. The pharmaceutical formulation of paragraph 32, wherein the solution further comprises arginine at a concentration of about 200 mM.

34. The pharmaceutical formulation of paragraph 18, wherein the solution comprises about 20 mM histidine and has a pH from about 5.5 to about 6.5.

35. The pharmaceutical formulation of paragraph 34, wherein the solution further comprises arginine at a concentration of about 200 mM.

36. The pharmaceutical formulation of any one of paragraphe 1-35 wherein the solution further comprises a surfactant at a concentration from about 0.001% (w/v) and about 0.1% (w/v).

37. The pharmaceutical formulation of paragraph 36, wherein the surfactant is a nonionic surfactant.

38. The pharmaceutical formulation of paragraph 37, wherein the surfactant is a polysorbate or a poloxamer.

39. The pharmaceutical formulation of paragraph 38, wherein the surfactant is polysorbate 80.

40. The pharmaceutical formulation of any one of paragraphe 1-39, wherein the formulation is stable when stored at between 2°C and 8°C for at least 6 months.

41. The pharmaceutical formulation of any one of paragraphe 1-39, wherein the formulation is stable when stored at between 2°C and 8°C for at least 12 months.

42. The pharmaceutical formulation of any one of paragraphe 1-39, wherein the viscosity is less than about 25 cP.

43. The pharmaceutical formulation of any one of paragraphe 1-39, wherein the viscosity is less than about 20 cP.

44. The pharmaceutical formulation of any one of paragraphe 1-39, wherein the viscosity is less than about 18 cP.

45. The pharmaceutical formulation of any one of paragraphe 1-39, wherein the injection glide force of the formulation is about 25 Newton or less when injected through a 27GA 1.25” needle at room température.

46. The pharmaceutical formulation of any one of paragraphe 1-39, wherein the injection glide force of the formulation is about 20 Newton or less when injected through a 25GA 1” needle at room température.

47. The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

about 20 mM sodium citrate, about 200mM L-arginine HCl, wherein the concentration of the antibody in the formulation is from about 175 mg/mL to about 195 mg/mL, and wherein the viscosity is less than about 25cP.

48. The pharmaceutical formulation of paragraph 47, wherein the formulation further comprises from 0.001% w/v to 0.05% w/v polysorbate 80.

49. The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

about 20mM L-histidine, about 200mM L-arginine HCl, wherein the concentration of the antibody in the formulation is from about 175 mg/mL to about 195 mg/mL, and wherein the viscosity is less than about 25cP.

50. The pharmaceutical formulation of paragraph 49, wherein the formulation further comprises from 0.001% w/v to 0.05% w/v polysorbate 80.

51. The pharmaceutical formulation of any one of paragraphe 1-50, wherein the formulation is stérile.

52. The pharmaceutical formulation of any one of paragraphe 1-50, wherein the monoclonal antibody is a full length monoclonal antibody.

53. The pharmaceutical formulation of paragraph 52, wherein the antibody is a human IgG4 full length antibody.

54. The pharmaceutical formulation of paragraph 53, wherein the IgG4 comprises a mutation in the hinge région.

55. The pharmaceutical formulation of any one of paragraphs 1-54, wherein the formulation does not include sucrose or sorbitol.

56. The pharmaceutical formulation of any one of paragraphs 1-54, wherein the formulation does not include CaCh.

57. The pharmaceutical formulation of any one of paragraphs 1-54, wherein the formulation does not include MgCh.

58. The pharmaceutical formulation of any one of paragraphs 1-54, wherein the formulation does not include CaCb and wherein the formulation does not include MgCh.

59. The pharmaceutical formulation of any of paragraphs 1-54, wherein the formulation does not include a divalent cation additive.

60. The pharmaceutical formulation of any one of paragraphs 1-59, wherein the concentration of the antibody is about 185 mg/mL.

61. The pharmaceutical formulation of any one of paragraphs 1-60, wherein the formulation further comprises a hyaluronidase enzyme in an amount effective to increase the dispersion and/or absorption of the antibody following subcutaneous administration.

62. The pharmaceutical formulation of paragraph 61, wherein the formulation comprises from about 100 U/mL to about 20,000 U/mL of said hyaluronidase enzyme.

63. The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

(a) polysorbate 80 at a concentration from about 0.01 to about 0.08% w/v;

(b) L-arginine HCl at a concentration from about 150 mM to about 200 mM;

(c) sodium citrate at a concentration from about 10 mM to about 50 mM; and (d) about 150 mg/mL to about 200 mg/mL of the antibody.

The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

(a) polysorbate 80 at a concentration from about 0.01 to about 0.08% w/v;

(b) L-arginine HCl at a concentration from about 150 mM to about 200 mM;

(c) L-histidine at a concentration from about 10 mM to about 50 mM; and (d) about 150 mg/mL to about 200 mg/mL of the antibody.

65. The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

(a) polysorbate 80 at a concentration of about 0.01 w/v;

(b) L-arginine HCI at a concentration of about 200 mM;

(c) sodium citrate at a concentration of about 20 mM; and (d) about 175 mg/mL to about 195 mg/mL of the antibody.

66. The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

(a) polysorbate 80 at a concentration of about 0.01% w/v;

(b) L-arginine HCl at a concentration of about 200 mM;

(c) L-histidine at a concentration of about 20 mM; and (d) about 175 mg/mL to about 195 mg/mL of the antibody.

67. The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

(a) polysorbate 80 at a concentration of about 0.01% w/v;

(b) L-arginine HCl at a concentration of about 200 mM;

(c) sodium citrate at a concentration of about 20 mM; and (d) about 175 mg/mL to about 195 mg/mL of the antibody.

68. The pharmaceutical formulation of paragraph 1, wherein the formulation comprises:

(a) polysorbate 80 at a concentration of about 0.01% w/v;

(b) L-arginine HCl at a concentration of about 200 mM;

(c) L-histidine at a concentration of about 20 mM; and (d) about 175 mg/mL to about 195 mg/mL of the antibody.

69. The pharmaceutical formulation of any of paragraphe 63 to 68 wherein the formulation further comprises from about 100 U/mL to about 20,000 U/mL of a hyaluronidase enzyme effective to increase the dispersion and/or absorption of the antibody following subcutaneous administration.

70. A stable aqueous pharmaceutical formulation suitable for parentéral administration to a mammalian subject, the formulation consisting essentially of:

(a) polysorbate 80 at a concentration from about 0.01 to about 0.08% w/v;

(b) L-arginine HCl at a concentration from about 150 mM to about 200 mM;

(c) sodium citrate at a concentration from about 10 mM to about 50 mM; and (d) a monoclonal antibody or fragment thereof that specifically binds to human MASP-2 at a concentration of about 150 mg/mL to about 200 mg/mL, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising CDR-H1, CDRH2 and CDR-H3 of SEQ ID NO:2 and (ii) a light chain variable région comprising CDR-L1, CDR-L2 and CDR-L3 of SEQ ID NO:3, or a variant thereof comprising a heavy chain variable région having at least 95% identity to SEQ ID NO:2 and a light chain variable région having at least 95% identity to SEQ ID NO:3;

wherein the formulation has a pH from about 5.0 to about 7.0, a viscosity of between 2 and 50 centipoise (cP), and wherein the formulation is stable when stored at between 2°C and 8°C for at least one month.

71. A stable aqueous pharmaceutical formulation suitable for parentéral administration to a mammalian subject, the formulation consisting essentially of:

(a) polysorbate 80 at a concentration from about 0.01 to about 0.08% w/v;

(b) L-arginine HCl at a concentration from about 150 mM to about 200 mM;

(c) L-histidine at a concentration from about 10 mM to about 50 mM; and (d) a monoclonal antibody or fragment thereof that specifically binds to human MASP-2 at a concentration of about 150 mg/mL to about 200 mg/mL, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising CDR-H1, CDRH2 and CDR-H3 of SEQ ID NO:2 and (ii) a light chain variable région comprising CDR-L1,

CDR-L2 and CDR-L3 of SEQ ID NO:3, or a variant thereof comprising a heavy chain variable région having at least 95% identity to SEQ ID NO:2 and a light chain variable région having at least 95% identity to SEQ ID NO:3;

wherein the formulation has a pH from about 5.0 to about 7.0, a viscosity of between 2 and 50 centipoise (cP), and wherein the formulation is stable when stored at between 2°C and 8°C for at least one month.

72. The formulation of any of paragraphe l-7l wherein the antibody or fragment thereof comprises a heavy chain variable région comprising the amino acid sequence set forth in SEQ ID NO:2 and a light chain variable région comprising the amino acid sequence set forth in SEQ ID NO:3.

73. A sealed container containing a formulation according to any one of paragraphe 1-72.

74. A subcutaneous administration device containing the formulation of any one of paragraphe 1-72 therein.

75. A kit comprising a pre-fdled container comprising the pharmaceutical formulation comprising the MASP-2 antibody of any of paragraphe 1-72 and instructions for use of the formulation.

76. The kit of paragraph 75 wherein the pre-filled container is selected from the group consisting of: a syringe, a pen injector, a sealed vial, an auto-injector and a pump device (e.g., an on-body patch pump or a tethered pump).

77. A kit comprising:

(a) a first pre-filled container comprising the pharmaceutical formulation comprising the MASP-2 antibody of any of paragraphe 1-60 or paragraphs 63-72;

(b) a second pre-filled container comprising an amount of hyaluronidase enzyme effective to increase the dispersion and/or absorption of the MASP-2 antibody following subcutaneous administration; and (c) instructions for use.

78. The kit of paragraph 77 wherein at least one of the first or second pre-filled container(s) is selected from the group consisting of: a syringe, a pen injector, a sealed vial, an auto-injector and a pump device (e.g., an on-body patch pump or a tethered pump).

79. A pharmaceutical unit dosage form suitable for parental administration to a human, comprising a formulation according to any of paragraphe 1-72 in a suitable container.

80. A method of treating a subject suffering from a disease or disorder amenable to treatment with a MASP-2 inhibitory antibody comprising administering a formulation of any one of paragraphe 1-72 to the subject in need thereof.

81. The method of paragraph 80, wherein the formulation is administered subcutaneously to the subject.

82. The method of paragraph 80, wherein the method further comprises administering to the subject a hyaluronidase enzyme in an amount effective to increase the dispersion and/or absorption of the antibody.

83. The method of paragraph 82, wherein the hyaluronidase enzyme is administered simultaneously with the formulation comprising the MASP-2 inhibitory antibody.

84. The method of paragraph 82 or 83, wherein the formulation comprises the MASP-2 inhibitory antibody and the hyaluronidase enzyme.

85. The method of paragraph 82, wherein the hyaluronidase enzyme is administered to the subject prior to the formulation comprising the MASP-2 inhibitory antibody.

86. The method of paragraph82, wherein the hyaluronidase enzyme is administered to the subject after the formulation comprising the MASP-2 inhibitory antibody.

The method of paragraph 80, wherein the formulation is administered via a pre-filled syringe containing the formulation therein.

88. A method of inhibiting MASP-2 dépendent complément activation in a subject suffering from, or at risk of developing, a complement-associated disease or disorder comprising administering a formulation of any one of paragraphe 1-72 to the subject in need thereof.

89. The method of paragraph 88, wherein the formulation is administered subcutaneously to the subject.

90. The method of paragraph 79, wherein the formulation is administered via a pre-filled syringe containing the formulation therein.

91. The method of paragraph 88, wherein the subject is suffering from or at risk of developing a complement-associated disease or disorder selected from the group consisting of a thrombotic microangiopathy (TMA), a rénal condition, an inflammatory reaction resulting from tissue or organ transplantation, an ischemia reperfusion injury, a complication associated with diabètes, a cardiovascular disease or disorder, an inflammatory gastrointestinal disorder, a pulmonary disorder, an ophthalmic disease or disorder, and disseminated intravascular coagulation.

92. The method of paragraph 91, wherein the thrombotic microangiopathy is atypical hemolytic syndrome (aHUS).

93. The method of paragraph 91, wherein the thrombotic microangiopathy is associated with hematopoietic stem cell transplant.

94. The method of paragraph 91, wherein the rénal condition is IgA nephropathy.

95. The method of paragraph 91, wherein the rénal condition is lupus nephritis.

96. A method of inhibiting MASP-2 dépendent complément activation in a subject suffering from, or at risk of developing, a complement-associated disease or disorder comprising diluting a formulation of any one of paragraphe 1-72 into a pharmaceuticallyacceptable diluent and administering the diluted formulation systemically to the subject in need thereof.

97. The method of paragraph 96, wherein the diluted formulation is administered intravenously to the subject.

98. The method of paragraph 96, wherein the subject is suffering from or at risk of developing a complement-associated disease or disorder selected from the group consisting of a thrombotic microangiopathy (TMA), a rénal condition, an inflammatory reaction resulting from tissue or organ transplantation, an ischemia reperfusion injury, a complication associated with diabètes, a cardiovascular disease or disorder, an inflammatory gastrointestinal disorder, a pulmonary disorder, an ophthalmic disease or disorder, and disseminated intravascular coagulation.

99. The method of paragraph 98, wherein the thrombotic microangiopathy is atypical hemolytic syndrome (aHUS).

100. The method of paragraph 98, wherein the thrombotic microangiopathy is associated with hematopoietic stem cell transplant.

101. The method of paragraph 98, wherein the rénal condition is IgA nephropathy.

102. The method of paragraph 98, wherein the rénal condition is lupus nephritis.

103. A pharmaceutical composition for use in treating a patient suffering from, or at risk for developing a MASP-2-dependent complement-associated disease or disorder, wherein the composition is a stérile, single-use dosage form comprising from about 350mg to about 400mg of MASP-2 inhibitory antibody, wherein the composition comprises about 1.8mL to about 2.2 mL of a 185mg/mL antibody formulation, wherein the antibody comprises (i) a heavy chain variable région comprising the amino acid sequence set forth in SEQ ID NO:2 and (ii) a light chain variable région comprising the amino acid sequence set forth in SEQ ID NO:3, and wherein the composition is stable when stored at between 2°C and 8°C for at least six months.

104. The composition of paragraph 103, wherein composition comprises a buffer System having a pH of 5.0 to 7.0.

105. The composition of paragraph 104, wherein the buffer System comprises at least one pharmaceutically acceptable buffering agent selected from the group consisting of succinate, histidine and citrate.

106. The composition of paragraph 103, wherein the composition comprises from 1.8mL to 2.2 mL of a 185 mg/mL MASP-2 inhibitory antibody formulation of any one of paragraphe 1-72.

107. The composition of any one of paragraphe 103-107, wherein the MASP-2 dépendent complement-associated disease or disorder is aHUS.

108. The composition of any one of paragraphe 103-107, wherein the MASP-2 dépendent complement-aesociated dieease or disorder is HSCT-TMA.

109. The composition of any one of paragraphe 103-107, wherein the MASP-2 dépendent complement-associated disease or disorder is IgAN.

110. The composition of any one of paragraphe 103-107, wherein the MASP-2 dépendent complement-associated disease or disorder is Lupus Nephritis (LN).

While the preferred embodiment of the invention has been illustrated and described, it will be appreciated that various changes can be made therein without departing from the spirit and scope of the invention.

Claims (5)

Claims

1. A stable pharmaceutical formulation suitable for parentéral administration to a mammalian subject, comprising:

(a) an aqueous solution comprising a buffer System having a pH of 5.0 to 7.0, wherein the buffer System comprises at least one buffering agent selected from the group consisting of citrate or histidine;

(b) a monoclonal antibody or fragment thereof that specifically binds to human MASP-2 at a concentration of about 50 mg/mL to about 250 mg/mL, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising the amino acid sequence set forth in SEQ ID NO:2 and (ii) a light chain variable région comprising the amino acid sequence set forth in SEQ ID NO:3; and (c) a tonicity modifying agent in a sufficient amount for the formulation to be hypertonie;

wherein the formulation has a viscosity of between 2 and 50 centipoise (cP), and wherein the formulation is stable when stored at between 2°C and 8°C for at least six months.

2. The pharmaceutical formulation of claim 1, wherein at least one or more of the following applies:

(a) wherein the concentration of the antibody in the formulation is from about 100 mg/mL to about 225 mg/mL, or from about 150 mg/mL to about 200 mg/mL, or from about 175 mg/mL to about 195 mg/mL;

(b) wherein the viscosity of the formulation is from about 2 cP to about 40 cP, or from about 2 cP to about 30 cP, or from about 2 cP to about 25 cP, or from about 2 cP to about 20 cP, or from about 2 cP to about 18 cP;

(c) wherein the viscosity is less than about 25 cP, or such as less than about 20 cP, or such as less than about 18 cP;

(d) wherein the concentration of the antibody is about 185 mg/mL;

(e) wherein the formulation is stable when stored between 2°C and 8°C for at least 12 months;

(f) wherein the injection glide force of the formulation is about 25 Newton or less when injected through a 27GA 1.25” needle at room température; and/or (g) wherein the injection glide force of the formulation is about 20 Newton or less when injected through a 25GA 1” needle at room température.

3. The pharmaceutical formulation of claim 1, wherein the at least one buffering agent is citrate, such as sodium citrate, such as wherein citrate is présent in the solution at a concentration of 10 mM to 50 mM.

4. The pharmaceutical formulation of claim 1, wherein the tonicity modifying agent is an amino acid with a charged side chain selected from the group consisting of:

(a) wherein the amino acid with a charged side chain is présent in the formulation at a concentration of from about 150 mM to about 300 mM;

(b) wherein the tonicity modifying agent is an amino acid with a negatively charged side chain; such as glutamate (c) wherein the tonicity modifying agent is an amino acid with a positively charged side chain, such as arginine or L-arginine-HCl, and (d) wherein arginine is présent in the solution at a hypertonie level of from 200 mM to 300 mM.

5. The pharmaceutical formulation of claim 3, wherein the solution comprises about 20 mM citrate and has a pH from about 5.5 to about 6.5, optionally wherein the solution further comprises arginine at a concentration of about 200 mM.

6. The pharmaceutical formulation of claim 1, wherein the solution further comprises a surfactant at a concentration from about 0.001% (w/v) and about 0.1% (w/v), optionally wherein the surfactant is a nonionic surfactant such as a polysorbate or a poloxamer, e.g., polysorbate 80

7. The pharmaceutical formulation of claim 1, wherein the formulation comprises:

about 20 mM sodium citrate, about 200 mM L-arginine HCl, wherein the concentration of the antibody in the formulation is from about 175 mg/mL to about 195 mg/mL, and wherein the viscosity is less than about 25cP, optionally wherein the formulation further comprises from 0.001% w/v to 0.05% w/v polysorbate 80.

8. The pharmaceutical formulation of claim 1, wherein the formulation is stérile.

9. The pharmaceutical formulation of claim 1, wherein the monoclonal antibody is a full length monoclonal antibody, optionally wherein the antibody is a human IgG4 full length antibody, such as a human IgG4 antibody comprising a mutation in the hinge région.

10. The pharmaceutical formulation of claim 1, wherein one or more the following applies:

(a) wherein the formulation does not include sucrose or sorbitol;

(b) wherein the formulation does not include CaCh;

(c) wherein the formulation does not include MgCb;

(d) wherein the formulation does not include CaCb and wherein the formulation does not include MgCb, and/or (e) wherein the formulation does not include a divalent cation additive.

11. The pharmaceutical formulation of claim 1, wherein the formulation is selected from the group consisting of:

(i) a formulation comprising (a) polysorbate 80 at a concentration from about 0.01 to about 0.08% w/v;

(b) L-arginine HCl at a concentration from about 150 mM to about 200 mM;

(c) sodium citrate at a concentration from about 10 mM to about 50 mM; and (d) about 150 mg/mL to about 200 mg/mL of the antibody; and (ii) a formulation comprising (a) polysorbate 80 at a concentration of about 0.01 w/v;

(b) L-arginine HCl at a concentration of about 200 mM;

(c) sodium citrate at a concentration of about 20 mM; and (d) about 175 mg/mL to about 195 mg/mL of the antibody.

12. A stable aqueous pharmaceutical formulation suitable for parentéral administration to a mammalian subject, the formulation consisting essentially of:

(a) polysorbate 80 at a concentration from about 0.01 to about 0.08% w/v;

(b) L-arginine HCl at a concentration from about 150 mM to about 200 mM;

(c) sodium citrate at a concentration from about 10 mM to about 50 mM; and (d) a monoclonal antibody or fragment thereof that specifically binds to human MASP-2 at a concentration of about 150 mg/mL to about 200 mg/mL, wherein said antibody or fragment thereof comprises (i) a heavy chain variable région comprising the amino acid sequence set forth in SEQ ID NO:2 and (ii) a light chain variable région comprising the amino acid sequence set forth in SEQ ID NO:3;

wherein the formulation has a pH from about 5.0 to about 7.0, a viscosity of between 2 and 50 centipoise (cP), and wherein the formulation is stable when stored at between 2°C and 8°C for at least six months.

13. A sealed container containing a formulation according to Claim 1 or 12.

14. A subcutaneous administration device containing the formulation of Claim 1 or 12 therein.

15. A kit comprising a pre-filled container comprising the pharmaceutical formulation comprising the MASP-2 antibody of Claim 1 or 12 and instructions for use of the formulation, such as wherein the pre-filled container is selected from the group consisting of: a syringe, a pen injector, a sealed vial, an auto-injector and a pump device, optionally wherein the kit further comprises at least one injection device suitable for administering the formulation in the sealed vial to a human subject.

16. A pharmaceutical unit dosage form suitable for parental administration to a human, comprising a formulation according to claim 1 or 12 in a suitable container.

17. Use of a formulation of claim 1 or 12 in the manufacture of a médicament for treating a subject suffering from a MASP-2-dependent complement-associated disease or disorder.

18. The use of claim 17, wherein the formulation is suitable for subcutaneous administration.

19. The use of claim 18, wherein the formulation is contained within a pre-filled syringe.

5 20. A pharmaceutical composition for use in treating a patient suffering from, or at risk for developing a MASP-2-dependent complement-associated disease or disorder, wherein the composition is a stérile, single-use dosage form comprising from about 350mg to about 400mg of MASP-2 inhibitory antibody, wherein the composition comprises about 1.8mL to about 2.2 mL of a 185mg/mL antibody formulation, wherein the antibody 10 comprises (i) a heavy chain variable région comprising the amino acid sequence set forth in SEQ ID NO:2 and (ii) a light chain variable région comprising the amino acid sequence set forth in SEQ ID NO:3, and wherein the composition is stable when stored at between 2°C and 8°C for at least six months.