AU2013202020B2 - Subcutaneous anti-HER2 antibody formulation - Google Patents

Abstract

Abstract The present invention relates to a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody, such as e.g. Trastuzumab (HERCEPINTM), Pertuzumab or T-DM1, or a mixture of such antibody molecules for 5 subcutaneous injection. In particular, the present invention relates to formulations comprising, in addition to a suitable amount of the anti-HER2 antibody, an effective amount of at least one hyaluronidase enzyme as a combined formulation or for use in form of a co-formulation. The said formulations comprise additionally at least one buffering agent, such as e.g. a histidine buffer, a stabilizer or a mixture of two or more stabilizers (e.g. a saccharide, such as 10 e.g. a,a-trehalose dihydrate or sucrose, and optionally methionine as a second stabilizer), a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. Methods for preparing such formulations and their uses thereof are also provided. 4179172_1 (GHMatters) P89111 .AU.1

Description

-2 Subcutaneous anti-HER2 antibody formulation The entire disclosure in the complete specification of our Australian Patent Application No. 2010277657 is by this cross-reference incorporated into the present specification. The present invention relates to highly concentrated, stable pharmaceutical 5 formulations of a pharmaceutically active anti-HER2 antibody or a mixture of such antibody molecules for subcutaneous injection. Such formulations comprise, in addition to the high amounts of anti-HER2 antibody or mixture thereof, a buffering agent, a stabilizer or a mixture of two ore more stabilizing agents, a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. The invention also relates to a process for the preparation 10 of the said formulation and to the uses of such formulation. The pharmaceutical use of antibodies has increased over the past years. In many instances such antibodies are injected via the intravenous (IV) route. Unfortunately the amount of antibody that can be injected via the intravenous route is limited by the physico chemical properties of the antibody, in particularly by its solubility and stability in a suitable 15 liquid formulation and by the volume of the infusion fluid. Alternative administration pathways are subcutaneous or intramuscular injection. These injection pathways require high protein concentration in the final solution to be injected [Shire, S.J., Shahrokh, Z. et al., "Challenges in the development of high protein concentration formulations", J. Pharm. Sci. 2004; 93(6): 1390-1402; Roskos, L.K., Davis C.G. et al., "The clinical pharmacology of 20 therapeutic antibodies", Drug Development Research 2004; 61(3): 108-120]. In order to increase the volume, and thereby the therapeutic dose, which can be safely and comfortably administered subcutaneously it has been proposed to use glycosaminoglycanase enzyme(s) in order to increase the interstitial space into which the antibody formulation can be injected [W02006/091871]. 25 Examples of stable formulations of pharmaceutically active antibodies for therapeutic use currently on the market are as follows: HERCEPTINTM (Trastuzumab) is a monoclonal antibody directed against the HER2 receptor (anti HER2 antibody) which is currently marketed in Europe in form of a 150 mg lyophilized powder (containing the antibody, a,a-trehalose dihydrate, L-histidine and L 30 histidine hydrochloride and polysorbate 20) which should be reconstituted for infusions with 4179172_1 (GHMallers) PS9111.AUA -3 water for injection to yield an injection dose of approximately 21 mg/ml. In the USA and many other countries a multiple dosage vial containing 440 mg Trastuzumab is marketed. AVASTINTM (Bevacizumab) is a monoclonal antibody directed against the vascular endothelial growth factor (VEGF) which is currently marketed in Europe as a liquid 5 formulation in two types of vials: a) 100 mg Bevacizumab in 4 ml and b) 400 mg Bevacizumab in 16 ml, respectively, providing a final concentration of 25 mg/ml in water for injection containing the following excipients: trehalose dihydrate, sodium phosphate and polysorbate 20. While the above antibody formulations have been found suitable for intravenous 10 administration there is a desire to provide highly concentrated, stable pharmaceutical formulations of therapeutically active antibodies for subcutaneous injection. The advantage of subcutaneous injections is that it allows the medical practitioner to perform it in a rather short intervention with the patient. Moreover the patient can be trained to perform the subcutaneous injection by himself. Such self-administration is particularly useful during 15 maintenance dosing because no hospital care is needed (reduced medical resource utilization). Usually injections via the subcutaneous route are limited to approximately 2 ml. For patients requiring multiple doses, several unit dose formulations can be injected at multiple sites of the body surface. The following two antibody products for subcutaneous administration are already on 20 the market. HUMIRATM (Adalimumab) is a monoclonal antibody directed against tumor necrosis factor alpha (TNF alpha) which is currently marketed in Europe in form of a 40 mg dose in 0.8 ml injection volume for subcutaneous application (concentration: 50 mg antibody /ml injection volume). 25 XOLAIRTM (Omalizumab) a monoclonal antibody directed against immunoglobulin E (anti IgE antibody) which is currently marketed in form of a 150 mg lyophilized powder (containing the antibody, sucrose, histidine and histidine hydrochloride monohydrate and polysorbate 20) which should be reconstituted with water for subcutaneous injection to yield a 125 mg/ml injection dose. 41791721 (GHMOtters) PS9111AU.1 -4 No highly concentrated, stable pharmaceutical anti-HER2 antibody formulation suitable for subcutaneous administration is currently available on the market. There is therefore a desire to provide such highly concentrated, stable pharmaceutical formulations of therapeutically active antibodies for subcutaneous injection. 5 The injection of parenteral drugs into the hypodermis is generally limited to volumes of less than 2 ml due to the viscoelastic resistance to hydraulic conductance in the subcutaneous (SC) tissue, due to the generated backpressure upon injection [Aukland K. and Reed R., "Interstitial-Lymphatic Mechanisms in the control of Extracellular Fluid Volume", Physiology Reviews", 1993; 73:1-78], as well as due to the perceptions of pain. 10 The preparation of high concentration protein formulations is rather challenging and there is a need to adapt each formulation to the particular proteins used because each protein has a different aggregation behavior. Aggregates are suspected to cause immunogenicity of therapeutic proteins in at least some of the cases. Immunogenic reaction against protein or antibody aggregates may lead to neutralizing antibodies which may render the therapeutic 15 protein or antibody ineffective. It appears that the immunogenicity of protein aggregates is most problematic in connection with subcutaneous injections, whereby repeated administration increases the risk of an immune response. While antibodies have a very similar overall structure, such antibodies differ in the amino acid composition (in particular in the CDR regions responsible for the binding to the 20 antigen) and the glycosylation pattern. Moreover there may additionally be post-translational modifications such as charge and glycosylation variants. In the particular case of anti-HER2 antibodies such post-translational modifications have been described e.g. for the humanized monoclonal antibody humMAb4D5-8 (= Trastuzumab). Particular purification methods for the removal of e.g. acidic variants have been developed and compositions comprising a 25 reduced amount of acidic variants (predominantly deamidated variants wherein one or more asparagine residue(s) of the original polypeptide have been converted to aspartate, i.e. the neutral amide side chain has been converted to a residue with an overall acidic character) have first been provided by Basey, C.D and Blank, G.S. in W099/57134. Stable lyophilized antibody formulations comprising a lyoprotectant, a buffer and a 30 surfactant have been described by Andya et al. (WO 97/04801 and US Patent Nos. 6,267,958, 6,685,940, 6,821,151 and 7,060,268). 4179172_1 (GHMaIers) P891 IIAV.1 -5 WO 2006/044908 provides antibody formulations, including monoclonal antibodies formulated in histidine-acetate buffer, pH 5.5 to 6.5, preferably 5.8 to 6.2. It is to be understood that, if any prior art publication is referred to herein, such reference does not constitute an admission that the publication forms a part of the common 5 general knowledge in the art, in Australia or any other country. SUMMARY The problem to be solved by the present invention is therefore to provide novel highly concentrated, stable pharmaceutical formulations of a pharmaceutically active anti-HER2 antibody or a mixture of such antibody molecules for subcutaneous injection. Such 10 formulations comprise, in addition to the high amounts of anti-HER2 antibody or mixture thereof, a buffering agent, a stabilizer or a mixture of two or more stabilizers, a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. The preparation of highly-concentrated antibody formulations is challenging because of a potential increase in viscosity at higher protein concentration and a potential increase in protein aggregation, a 15 phenomenon that is per se concentration-dependent. High viscosities negatively impact the process ability (e.g. pumping and filtration steps) of the antibody formulations and the administration (e.g. the syringe ability). By the addition of excipients high viscosities could be decreased in some cases. Control and analysis of protein aggregation is an increasing challenge. Aggregation is potentially encountered during various steps of the manufacturing 20 process, which include fermentation, purification, formulation and during storage. Different factors, such as temperature, protein concentration, agitation stress, freezing and thawing, solvent and surfactant effects, and chemical modifications, might influence the aggregation behavior of a therapeutic protein. During development of a highly concentrated antibody formulation the aggregation tendency of the protein has to be monitored and controlled by the 25 addition of various excipients and surfactants [Kiese S. et al., J. Pharm. Sci., 2008; 97(10); 4347-4366]. The challenge to prepare suitable highly concentrated, stable pharmaceutical formulation of the pharmaceutically active anti-HER2 antibody in accordance with the present invention is increased by the fact that two different proteins have to be formulated in one liquid formulation in such a way that the formulation remains stable over several weeks 30 and the pharmaceutically active ingredients remain active during proper storage. 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -6 A first aspect provides a highly concentrated, stable pharmaceutical liquid formulation of a pharmaceutically active anti-HER2 antibody for subcutaneous injection comprising: a. about 120 + 18 mg/ml Trastuzumab; b. about I to 50 mM of histidine/HCl providing a pH of 5.5 + 0.6; 5 c. about 15 to 250 mM of a,a-trehalose dihydrate or sucrose and about 5 to 25 mM of methionine; and d. about 0.01 to 0.08 % of a nonionic surfactant, wherein the highly concentrated, stable pharmaceutical liquid formulation lacks a hyaluronidase enzyme. 10 A second aspect provides a highly concentrated, stable pharmaceutical liquid formulation of a pharmaceutically active anti-HER2 antibody for subcutaneous injection essentially consisting of 120 mg/ml Trastuzumab, 20 mM L-histidine/HCl pH 5.5, 210 mM a,a-trehalose dihydrate, 10 mM methionine and 0.04% polysorbate 20. A third aspect provides a pharmaceutical formulation comprising a highly concentrated, 15 stable pharmaceutical anti-HER2 antibody liquid formulation according to the first or second aspect combined with 150 to about 16'000 U/ml, 2'000 U/ml, or 12'000 U/ml of a hyaluronidase enzyme. A fourth aspect provides use of: a. about 120 + 18 mg/ml Trastuzumab; 20 b. about I to 50 mM of histidine/HCl providing a pH of 5.5 + 0.6; c. about 15 to 250 mM of a,a-trehalose dihydrate or sucrose and about 5 to 25 mM of methionine; and d. about 0.01 to 0.08 % of a nonionic surfactant, in the manufacture of a medicament for treating in a subject a disease or disorder 25 amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease, wherein the medicament lacks a hyaluronidase enzyme. A fifth aspect provides use of a formulation according to the first to third aspects in the manufacture of a medicament for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease. 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -7 A sixth aspect provides use of a formulation according to the first or second aspect in combination with a hyaluronidase enzyme in the manufacture of a medicament for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease. 5 A seventh aspect provides use of a formulation according to the first or second aspect in combination with 10 mg/ml rHuPH20 in 20 mM His/Histidine HCl, pH 6.5, 130 mM NaCl, 0.05% (w/v) polysorbate 80 in the manufacture of a medicament for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease. 10 An eighth aspect provides a method for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease, comprising administering to the subject a formulation according to the first to third aspects in an amount effective to treat the disease or disorder. A ninth aspect provides a method for treating in a subject a disease or disorder 15 amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease, comprising administering to the subject a formulation according to the first or second aspect in combination with a hyaluronidase enzyme. A tenth aspect provides a method for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant 20 disease, comprising administering to the subject a formulation according to the first or second aspect in combination with 10 mg/ml rHuPH20 in 20 mM His/Histidine HCl, pH 6.5, 130 mM NaCl, 0.05% (w/v) polysorbate 80. An eleventh aspect provides an injection device comprising a formulation according to the first or second aspect. 25 A twelfth aspect provides an injection device comprising a formulation according to the third aspect. A thirteenth aspect provides a kit comprising one or more vials containing a formulation according to the first or second aspect, optionally when used according to a method according to any one of the eighth to tenth aspects. 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -7a A fourteenth aspect provides a kit comprising one or more vials containing a formulation according to the third aspect, optionally when used according to a method according to the eighth aspect. A fifteenth aspect provides a kit comprising the injection device according to the 5 eleventh or twelfth aspects. Disclosed herein is a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody or a mixture of such antibody molecules for subcutaneous injection, which is ready for use. More particularly the highly concentrated, stable pharmaceutical formulation of a 10 pharmaceutically active anti-HER2 antibody formulation may comprise: - about 50 to 350 mg/ml anti-HER2 antibody; - about I to 100 mM of a buffering agent providing a pH of 5.5 ± 2.0; - about I to 500 mM of a stabilizer or a mixture of two or more stabilizers, whereby optionally methionine is present as a secondary stabilizer e.g. in a concentration of 15 5 to 25 mM; - 0.01 to 0.1 % of a nonionic surfactant; and - an effective amount of at least one hyaluronidase enzyme. Also disclosed is use of a formulation for the preparation of a medicament useful for treating a disease or disorder amenable to treatment with an anti-HER2 antibody such as e.g. 20 cancer or a non-malignant disease in a subject comprising administering the formulation described herein to a subject in an amount effective to treat the said disease or disorder. The anti-HER2 antibody can be co-administered concomitantly or sequentially with a chemotherapeutic agent. Also disclosed are methods of treating a disease or disorder which is amenable to 25 treatment with an anti-HER2 antibody (e.g. cancer or a non-malignant disease) in a subject comprising administering the formulation described herein to a subject in an amount effective to treat the said disease or disorder. The cancer or a non-malignant disease will generally 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -7b involve HER2-expressing cells, such that the HER2 antibody in the therapeutic pharmaceutical SC formulation in accordance with the present disclosure is able to bind to the affected cells. Also disclosed are pharmaceutical compositions consisting of a highly concentrated, 5 stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody or a mixture of such antibody and a suitable amount of at least one hyaluronidase enzyme in the form of a kit comprising both injection components and suitable instructions for their subcutaneous administration. Also disclosed are injection devices comprising a highly concentrated, stable 10 pharmaceutical formulation in accordance with the present invention. Such formulation may consist of a pharmaceutically active anti-HER2 antibody or a mixture of such antibody molecules and suitable excipients as outlined below and may additionally comprise a soluble hyaluronidase glycoprotein either as a combined formulation or as a separate formulation for co-administration. 15 DETAILED DESCRIPTION The highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody formulation may be provided in liquid form or may be provided in lyophilized form. In accordance with the teachings in WO 97/04801 the antibody concentration in the reconstituted formulation can be increased by reconstitution of a 20 lyophilized formulation to provide a protein concentration in the reconstituted formulation which is about 2-40 times greater than the protein concentration in the mixture before the lyophilization step. The anti-HER2 antibody concentration is 100 to 150 mg/ml, e.g. 120 ± 18 mg/ml, about 110 mg/ml, about 120 mg/ml or about 130 mg/ml. 25 The concentration of the buffering agent providing a pH of 5.5 ± 2.0 is I to 50 mM, e.g. 10 to 30 mM or about 20 mM. Various buffering agents are known to the person skilled in the art as outlined further below. The buffering agent can be a histidine buffer, e.g. L histidine/HCl. In a particular embodiment the pH of the L-histidine/HCl buffer is about 5.5 or about 6.0. 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -7c The stabilizer (used synonymously with the term "stabilizing agent" in the present patent description) is e.g. a carbohydrate or saccharide or a sugar admitted by the authorities as a suitable additive or excipient in pharmaceutical formulations, e.g. a,a-trehalose dihydrate or sucrose. The concentration of the stabilizer is 15 to 250 mM, or 150 to 250 mM, or about 5 210 mM. The formulation may contain a secondary stabilizer, whereby this secondary stabilizer can be methionine, e.g in a concentration of 5 to 25 mM or in a concentration of 5 to 15 mM (e.g. methionine in a concentration of about 5mM, about 10 mM or about 15 mM). Suitable examples of pharmaceutically acceptable surfactants include polyoxyethylen sorbitan fatty acid esters (Tween), polyethylene-polypropylene glycols, polyoxyethylene 10 stearates, polyoxyethylene alkyl ethers, e.g. polyoxyethylene monolauryl ether, 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -8 alkylphenylpolyoxyethylene ethers (Triton-X), polyoxyethylene-polyoxypropylene copolymer (Poloxamer, Pluronic), and sodium dodecyl sulphate (SDS). Most suitable polyoxyethylenesorbitan-fatty acid esters are polysorbate 20, (sold under the trademark Tween 20TM) and polysorbate 80 (sold under the trademark Tween 80TM). Most suitable 5 polyethylene-polypropylene copolymers are those sold under the names Pluronic@ F68 or Poloxamer 188TM. Most suitable polyoxyethylene alkyl ethers are those sold under the trademark BrijTM. Most suitable alkylphenolpolyoxyethylene ethers are sold under the trade name Triton-X. The nonionic surfactant can be a polysorbate, e.g. selected from the group of polysorbate 20, polysorbate 80 and polyethylene-polypropylene copolymer. The 10 concentration of the nonionic surfactant is 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 0.02, 0.04 or 0.06 % (w/v). The concentration of the hyaluronidase enzyme depends on the actual hyaluronidase enzyme used in the preparation of the formulation in accordance with the invention. An effective amount of the hyaluronidase enzyme can easily be determined by the person skilled 15 in the art based on the disclosure further below. It should be provided in sufficient amount so that an increase in the dispersion and absorption of the co-administered anti-HER2 antibody is possible. The minimal amount of the hyaluronidase enzyme is > 150 U/ml. More particularly the effective amount of the hyaluronidase enzyme is about 1'000 to 16'000 U/ml, whereby the said amount corresponds to about 0.01 mg to 0.16 mg protein based on an 20 assumed specific activity of 100'000 U/mg. Alternatively the concentration of the hyaluronidase enzyme is about 1'500 to 12'000 U/ml, or more particularly about 2'000 U/ml or about 12'000 U/ml. The amounts specified hereinbefore correspond to the amount of hyaluronidase enzyme initially added to the formulation. As evidenced in the example formulations the hyaluronidase enzyme concentrations measured in the final formulation may 25 vary within a certain range. Thus, e.g. the actually measured hyaluronidase enzyme (HE) concentration measured just after adding 12'000 U/ml of enzyme showed variations between 12355 U/ml to 15178 U/ml (see Tables 1 Formulations A to F and Table 3 Formulation H). The hyaluronidase enzyme is present either as a combined final formulation or for use for co administration, e.g. as a co-formulation as further outlined below. The important issue for the 30 formulation in accordance with the present invention is that at the time it is ready for use and/or is injected it has the composition as set out in the appended claims. The ratio (w/w) of the hyaluronidase enzyme to the anti-HER2 antibody is in the range of 1 : 1'000 to 1 : 8'000, or in the range of 1 : 4'000 to 1 : 5'000 or about 1 : 6'000. 4179172_1 (GHMatters) P891 11.AU.1 -9 The hyaluronidase enzyme may be derived from animals, human samples or manufactured based on the recombinant DNA technology as described further below. In some embodiments the highly concentrated, stable pharmaceutical anti-HER2 antibody formulations in accordance with the present invention have one of the following 5 compositions: a) 100 to 150 mg/ml anti-HER2 antibody, e.g. selected from the group of Trastuzumab, Pertuzumab and T-DM1; I to 50 mM of a histidine buffer, e.g. L-histidine / HC1 at a pH of about 5.5; 15 to 250 mM of a stabilizer which is e.g. a,a-trehalose dihydrate, and optionally methionine as a second stabilizer at 10 a concentration of 5 to 25 mM; about 0.01 to 0.08 % of a nonionic surfactant; and >150 to 16'000 U/ml, more particularly 1'000 to 16'000 U/ml of a hyaluronidase enzyme such as e.g. rHuPH20, e.g. at a concentration of about 2'000 U/mi or about 12'000 U/ml. b) 120 ± 18 mg/ml anti-HER2 antibody, e.g. selected from the group of 15 Trastuzumab, Pertuzumab and T-DMI; 10 to 30 mM, or about 20 mM of a histidine buffer such as e.g. L-histidine / HCl at a pH of about 5.5; 150 to 250 mM or about 210 mM of a stabilizer, which is e.g. a,a-trehalose dihydrate, and optionally methionine as a second stabilizer at a concentration of 5 to 25 mM, or 5 to 15 mM, or about 10 mM; about 0.01 to 0.08 % of a nonionic surfactant; 20 and 1'000 to 16'000 U/ml, or 1'500 to 12'000 U/ml, about 2'000 U/ml or about 12'000 U/ml of a hyaluronidase enzyme such as e.g. rHuPH20. c) About 120 mg/ml anti-HER2 antibody, e.g. selected from the group of Trastuzumab, Pertuzumab and T-DM1; 10 to 30 mM, or about 20 mM of a histidine buffer, such as e.g. L-histidine / HCi at a pH of about 5.5; 150 to 250 25 mM, e.g. about 210 mM of a stabilizer, which is e.g. a,a-trehalose dihydrate, and optionally methionine as a second stabilizer at a concentration of 5 to 25 mM, or 5 to 15 mM, or about 10 mM; about 0.01 to 0.08 % of a nonionic surfactant; and 1'000 to 16'000 U/ml, or 1'500 to 12'000 U/ml, or more particularly about 2'000 U/ml or about 12'000 U/ml of a hyaluronidase 30 enzyme such as e.g. rHuPH20. 4179172_ (GHMatters) P809 1 .AU.1 -10 d) About 120 mg/mI anti-HER2 antibody, e.g. selected from the group of Trastuzumab, Pertuzumab and T-DM1; about 20 mM of a histidine buffer such as e.g. L-histidine / HCl at a pH of about 5.5; about 210 mM a,a-trehalose dihydrate, and optionally about 10 mM methionine as a second stabilizer; 0.04 5 or 0.06 % of polysorbate 20; and about 12'000 U/ml of a hyaluronidase enzyme such as rHuPH20; and particularly the Formulation A specified below. e) About 120 mg/ml anti-HER2 antibody, e.g. selected from the group of Trastuzumab, Pertuzumab and T-DM1; about 20 mM of a histidine buffer such as e.g. L-histidine / HCl at a pH of about 5.5; about 210 mM a,a-trehalose 10 dihydrate, and optionally 10 mM methionine as a second stabilizer; 0.04 or 0.06 % of polysorbate 20; and about 2'000 U/ml of a hyaluronidase enzyme such as rHuPH20; and particularly the Formulation X specified below. A lyophilized formulation comprising 120 mg/ml anti-HER2 antibody, e.g. selected from the group of Trastuzumab, Pertuzumab and T-DM1; 20 mM of a 15 histidine buffer such as e.g. L-histidine /HCL at a pH of about 5.5; 210 mM of a,a-trehalose dihydrate and optionally 10 mM methionine as a second stabilizer; about 0.04 to 0.06 % of a nonionic surfactant; and particularly Formulation Y specified below. These formulations can be reconstituted with 1'000 to 16'000 U/ml, or l'500 to 12'000 U/ml, or more particularly about 20 2'000 U/ml or about 12'000 U/ml of a hyaluronidase enzyme such as e.g. rHuPH20. In another embodiment the highly concentrated, stable pharmaceutical anti-HER2 antibody formulations in accordance with the present invention have one of the compositions specified in Table 1, 3 and 4, whereby the formulations C, D, E and F are less preferred 25 because of less desired properties as outlined in the Examples and in Table 1. It has been proposed to facilitate the subcutaneous injection of therapeutic proteins and antibodies by using small amounts of soluble hyaluronidase glycoproteins (sHASEGPs); see W02006/091871. It has been shown that the addition of such soluble hyaluronidase glycoproteins (either as a combined formulation or by co-administration) facilitates the 30 administration of therapeutic drug into the hypodermis. By rapidly depolymerizing hyaluronan HA in the extracellular space sHASEGP reduces the viscosity of the interstitium, 41791721 (GHMAtters) P89111AU.l -11 thereby increasing hydraulic conductance and allowing for larger volumes to be administered safely and comfortably into the subcutaneous tissue. The increased hydraulic conductance induced by sHASEGP through reduced interstitial viscosity allows for greater dispersion, potentially increasing the systemic bioavailability of SC administered therapeutic drug. 5 The highly concentrated, stable pharmaceutical formulations of the present invention comprising a soluble hyaluronidase glycoprotein are therefore particularly suited for subcutaneous injection. It is clearly understood by the person skilled in the art that such a formulation comprising an anti-HER2 antibody and a soluble hyaluronidase glycoprotein can be provided for administration in form of one single combined formulation or alternatively in 10 form of two separate formulations which can be mixed just prior to the subcutaneous injection. Alternatively the anti-HER2 antibody and the soluble hyaluronidase glycoprotein can be administered as separate injections at different sites of the body, preferably at sites which are immediately adjacent to each other. It is also possible to inject the therapeutic agents present in the formulation in accordance with the present invention as consecutive 15 injections, e.g. first the soluble hyaluronidase glycoprotein followed by the injection of the anti-HER2 antibody formulation. These injections can also be performed in the reversed order, viz. by first injecting the anti-HER2 antibody formulation followed by injecting the soluble hyaluronidase glycoprotein. In case the anti-HER2 antibody and the soluble hyaluronidase glycoprotein are administered as separate injections, one or both of the 20 proteins have to be provided with the buffering agent, the stabilizer(s) and the nonionic surfactant in the concentrations as specified in the appended claims but excluding the hyaluronidase enzyme. The hyaluronidase enzyme can then be provided e.g. in a L-histidine / HCl buffer at pH of about 6.5, 100 to 150 mM NaCl and 0.01 to 0.1 % (w/v) polysorbate 20 or polysorbate 80. In particular the hyaluronidase enzyme is provided in 20 mM L-histidine / 25 HCI buffer at pH 6.5, 130 mM NaCl, 0.05 % (w/v) polysorbate 80 as specifically exemplified in Formulation G of Table I below. As noted above the soluble hyaluronidase glycoprotein may be considered to be a further excipient in the anti-HER2 formulation. The soluble hyaluronidase glycoprotein may be added to the anti-HER2 formulation at the time of manufacturing the anti-HER2 30 formulation or may be added shortly before the injection. Alternatively the soluble hyaluronidase glycoprotein may be provided as a separate injection. In the latter case the soluble hyaluronidase glycoprotein may be provided in a separate vial either in lyophilized 41791721 (GHMatters) PS9111.AU.1 -12 form which must be reconstituted with suitable diluents before the subcutaneous inj ection takes place, or may be provided as a liquid formulation by the manufacturer. The anti-HER2 formulation and the soluble hyaluronidase glycoprotein may be procured as separate entities or may also be provided as kits comprising both injection components and suitable 5 instructions for their subcutaneous administration. Suitable instructions for the reconstitution and / or administration of one or both of the formulations may also be provided. Therefore, also disclosed are pharmaceutical compositions consisting of a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody or a mixture of such antibody and a suitable amount of at least one hyaluronidase 10 enzyme in the form of a kit comprising both injection components and suitable instructions for their subcutaneous administration. Also disclosed are injection devices comprising a highly concentrated, stable pharmaceutical formulation in accordance with the present invention. Such formulation may consist of a pharmaceutically active anti-HER2 antibody or a mixture of such antibody 15 molecules and suitable excipients as outlined below and may additionally comprise a soluble hyaluronidase glycoprotein either as a combined formulation or as a separate formulation for co-administration. A variety of anti-HER2 antibodies are known in the prior art. Such antibodies are preferably monoclonal antibodies. They may either be so-called chimaeric antibodies, 20 humanized antibodies or fully human antibodies. They may either be full length anti-HER2 antibodies; anti-HER2 antibody fragments having the same biological activity; including amino acid sequence variants and / or glycosylation variants of such antibodies or fragments. Examples of humanized anti-HER2 antibodies are known under the INN names Trastuzumab and Pertuzumab. Another suitable anti-HER2 antibody is T-DM1, which is an antibody-toxin 25 conjugate consisting of huMAb4D5-8 (HERCEPIN T M ) and a maytansinoide (viz. DM1 = N deacetyl-N 2 -(3-mercapto-1-oxopropyl)-maytansine; a highly potent antimicrotubule agent) which conjugate (with a MCC linker) is currently under development for metastatic breast cancer. Other HER2 antibodies with various properties have been described in Tagliabue et al., Int. J. Cancer, 47:933-937 (1991); McKenzie et al., Oncogene, 4:543-548 (1989); Cancer 30 Res., 51:5361-5369 (1991); Bacus et al., Molecular Carcinogenesis, 3:350-362 (1990); Stancovski et al., PNAS (USA), 88:8691-8695 (1991); Bacus et al., Cancer Research, 52:2580-2589 (1992); Xu et al., Int. J. Cancer, 53:401-408 (1993); W094/00136; Kasprzyk 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -13 et al., Cancer Research, 52:2771-2776 (1992); Hancock et al., Cancer Res., 51:4575-4580 (1991); Shawver et al., Cancer Res., 54:1367-1373 (1994); Arteaga et al., Cancer Res., 54:3758-3765 (1994); Harwerth et al., J. Biol. Chem., 267:15160-15167 (1992); U.S. Pat. No. 5,783,186; and Klapper et al., Oncogene, 14:2099-2109 (1997). The most successful 5 therapeutic anti-HER2 antibody is Trastuzumab sold by Genentech Inc. and F. Hoffmann-La Roche Ltd under the trade name HERCEPINTM. Further details on the HER2 antigen and antibodies directed thereto are described in many patent and non-patent publications (for a suitable overview see U.S. Patent No. 5,821,337 and WO 2006/044908). The anti-HER2 antibody is e.g. selected from the group of Trastuzumab, Pertuzumab 10 and T-DM1 and may also consist of a mixture of anti-HER2 antibodies such as e.g. Trastuzumab and Pertuzumab or T-DM 1 and Pertuzumab. It has been found that the combination of Pertuzumab and Trastuzumab is active and well tolerated in patients with metastatic HER2-positive breast cancer who had experienced progression during prior trastuzumab therapy [se e.g. Baselga, J. et al., Journal of Clin. Oncol. Vol 28 (7) 2010: pp. 15 1138-1144]. The formulation in accordance with the present invention is exemplified herein with the anti-HER2 antibody Trastuzumab. The terms "Trastuzumab", "Pertuzumab" and "T DM1" encompass all corresponding anti-HER2 antibodies that full-fill the requirements necessary for obtaining a marketing authorization as an identical or biosimilar product in a country or territory selected from the group of countries consisting of the USA, Europe and 20 Japan. Trastuzumab has the CDR regions defined in EP-B-590058. Pertuzumab has the CDR regions defined in WO 01/00245. The activity of Trastuzumab in the BT-474 antiproliferation assay [Nahta, R. et al., "The HER-2-targeting antibodies Trastuzumab and Pertuzumab synergistically inhibit the survival of breast cancer cells", Cancer Res. 2004; 64:2343.2346] has been found to be between 0.7 - 1.3 x 10 4 U/mg. T-DM1 is described in 25 WO 2005/117986. HERCEPINTM (Trastuzumab) has been approved in the EU for the treatment of patients with metastatic breast cancer (MBC) who have tumors that overexpress HER2 as follows: - As monotherapy for the treatment of patients who have received at least two chemotherapy regimens for their metastatic disease. Prior chemotherapy must have 30 included at least an anthracycline and a taxane unless patients are unsuitable for these treatments. Hormone receptor-positive patients must also have failed hormonal therapy, unless patients are unsuitable for these treatments. 4179172_1 (GHMaUers) P89111.AU.1 -14 - In combination with paclitaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease and for whom an anthracycline is not suitable. - In combination with docetaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease. 5 - In combination with an aromatase inhibitor for the treatment of postmenopausal patients with hormone receptor-positive MBC not previously treated with Trastuzumab. Trastuzumab has also been approved in the EU for the treatment of patients with MBC who have tumors that overexpress HER2 for the treatment of patients with HER2-positive early-stage breast cancer (EBC) following surgery, chemotherapy (neoadjuvant or adjuvant) 10 and radiotherapy (if applicable). Moreover Trastuzumab is currently being developed for the treatment of gastric cancer. Two dosing regimens are currently approved for Trastuzumab (Table 1); once weekly (qlw) and every 3 weeks (q3w) for both metastatic breast cancer (MBC) and early breast cancer (EBC). In the qlw dosing regime the loading dose is 4 mg/kg followed by subsequent 15 dose at 2 mg/kg. In the q3w dosing regime the loading dose is 8 mg/kg followed by subsequent dose at 6 mg/kg. As noted above HERCEPINTM (Trastuzumab) for intravenous administration is currently sold in lyophilized form in vials. In the formulation sold in Europe each vial contains the dry residue obtained after lyophilization of a filling volume of 6.25 ml of a 20 sterile aqueous solution containing the following components: 150 mg Trastuzumab (effective 156.3 mg to ensure that the nominal quantity of 150 mg can be withdrawn from the final product after reconstitution), 3.50 mg L-histidine hydrochloride, 2.25 mg L-histidine, 141.9 mg a,a-trehalose dihydrate, 0.63 mg Polysorbate 20. The dissolved lyophilisate contains about 24 mg/ml Trastuzumab, 5 mM L-histidine/HCl pH 6.0, 60 mM a,a-trehalose 25 dihydrate, 0.01% polysorbate 20. The solution is then added to the infusion solution and then the infusion is administered to the patient over 90 minutes (subsequent infusions can be given over 30 minutes in MBC, if well tolerated). A179172 1 (GHMatters) P89111AUA -15 A number of a soluble hyaluronidase glycoprotein are known in the prior art. In order to further define the function, the mechanism of action and the properties of such soluble hyaluronidase glycoproteins the following background information is provided. The SC (hypodermal) interstitial matrix is comprised of a network of fibrous proteins 5 embedded within a viscoelastic gel of glycosaminoglycans. Hyaluronan (HA), a non-sulfated repeating linear disaccharide, is the prominent glycosaminoglycan of the SC tissue. HA is secreted into the interstitium by fibroblasts as a high molecular weight, megadalton viscous polymer that is subsequently degraded locally, in the lymph, and in the liver, through the action of lysosomal hyaluronidases and exoglycosidases. Approximately 50% of the 10 hyaluronan in the body is produced by the SC tissue, where it is found at approximately 0.8 mg/gm wet weight tissue [Aukland K. and Reed R., supra]. It is estimated that the average 70 kg adult contains 15 grams of HA, of which 30 percent is turned over (synthesized and degraded) daily [Laurent L.B., et al., "Catabolism of hyaluronan in rabbit skin takes place locally, in lymph nodes and liver", Exp. Physiol. 1991; 76: 695-703]. As a major constituent 15 of the gel-like component of the hypodermal matrix, HA contributes significantly to its viscosity. Glycosaminoglycans (GAGs) are complex linear polysaccharides of the extracellular matrix (ECM). GAGs are characterized by repeating disaccharide structures of an N substituted hexosamine and an uronic acid (in the case of hyaluronan (HA), chondroitin 20 sulfate (CS), chondroitin (C), dermatan sulfate (DS), heparan sulfate (HS), and heparin (H)), or a galactose (in the case of keratan sulfate (KS)). Except for HA, all exist covalently bound to core proteins. The GAGs with their core proteins are structurally referred to as proteoglycans (PGs). Hyaluronan (HA) is found in mammals predominantly in connective tissues, skin, 25 cartilage, and in synovial fluid. Hyaluronan is also the main constituent of the vitreous of the eye. In connective tissue, the water of hydration associated with hyaluronan creates hydrated matrices between tissues. Hyaluronan plays a key role in biological phenomena associated with cell motility including rapid development, regeneration, repair, embryogenesis, embryological development, wound healing, angiogenesis, and tumorigenesis (Toole, Cell 30 Biol. Extracell. Matrix, Hay (ed), Plenum Press, New York, 1991; pp. 1384-1386; Bertrand et al., Int. J. Cancer 1992; 52:1-6; Knudson et al., FASEB J. 1993; 7:1233-1241]. In addition, hyaluronan levels correlate with tumor aggressiveness [Ozello et al., Cancer Res. 1960; 4179172_1 (GHMatters) P69111.AU.1 -16 20:600-604; Takeuchi et al., Cancer Res. 1976; 36:2133-2139; Kimata et al., Cancer Res. 1983; 43:1347-1354]. HA is found in the extracellular matrix of many cells, especially in soft connective tissues. HA has been assigned various physiological functions, such as in water and plasma 5 protein homeostasis [Laurent T.C. et al., FASEB J., 1992; 6: 2397-2404]. HA production increases in proliferating cells and may play a role in mitosis. It has also been implicated in locomotion and cell migration. HA seems to play important roles in cell regulation, development, and differentiation [Laurent et al., supra]. HA has widely been used in clinical medicine. Its tissue protective and theological 10 properties have proved useful in ophthalmic surgery (e.g. to protect the corneal endothelium during cataract surgery). Serum HA is diagnostic of liver disease and various inflammatory conditions, such as rheumatoid arthritis. Interstitial edema caused by accumulation of HA may cause dysfunction in various organs [Laurent et al., supra]. Hyaluronan protein interactions also are involved in the structure of the extracellular 15 matrix or "ground substance". Hyaluronidases are a group of generally neutral- or acid-active enzymes found throughout the animal kingdom. Hyaluronidases vary with respect to substrate specificity, and mechanism of action (WO 2004/078140). There are three general classes of hyaluronidases: 20 1. Mammalian-type hyaluronidases, (EC 3.2.1.35) which are endo-beta-N acetylhexosaminidases with tetrasaccharides and hexasaccharides as the major end products. They have both hydrolytic and transglycosidase activities, and can degrade hyaluronan and chondroitin sulfates (CS), generally C4-S and C6-S. 2. Bacterial hyaluronidases (EC 4.2.99.1) degrade hyaluronan and, and to various extents, CS 25 and DS. They are endo-beta-N-acetylhexosaminidases that operate by a beta elimination reaction that yields primarily disaccharide end products. 3. Hyaluronidases (EC 3.2.1.36) from leeches, other parasites, and crustaceans are endo-beta glucuronidases that generate tetrasaccharide and hexasaccharide end products through hydrolysis of the beta 1-3 linkage. 4179172_1 (GHMaters) P89111.AU.1 -17 Mammalian hyaluronidases can be further divided into two groups: neutral-active and acid-active enzymes. There are six hyaluronidase-like genes in the human genome, HYAL, HYAL2, HYAL3, HYAL4, HYALPI and PH20/SPAM1. HYALPI is a pseudogene, and HYAL3 has not been shown to possess enzyme activity toward any known substrates. 5 HYAL4 is a chondroitinase and exhibits little activity towards hyaluronan. HYALl is the prototypical acid-active enzyme and PH20 is the prototypical neutral-active enzyme. Acid active hyaluronidases, such as HYALI and HYAL2 generally lack catalytic activity at neutral pH (i.e. pH 7). For example, HYALI has little catalytic activity in vitro over pH 4.5 [Frost I.G. and Stem, R., "A microtiter-based assay for hyaluronidase activity not requiring 10 specialized reagents", Anal. Biochemistry, 1997; 251:263-269]. HYAL2 is an acid-active enzyme with a very low specific activity in vitro. The hyaluronidase-like enzymes can also be characterized by those which are generally locked to the plasma membrane via a glycosylphosphatidyl inositol anchor such as human HYAL2 and human PH20 [Danilkovitch-Miagkova et al., Proc. Natl. Acad. Sci. U SA, 2003; 15 100(8):4580-4585; Phelps et al., Science 1988; 240(4860): 1780-1782], and those which are generally soluble such as human HYALl [Frost, I.G. et al., "Purification, cloning, and expression of human plasma hyaluronidase", Biochem. Biophys. Res. Commun. 1997; 236(l):10-15]. However, there are variations from species to species: bovine PH20 for example is very loosely attached to the plasma membrane and is not anchored via a 20 phospholipase sensitive anchor [Lalancette et al., Biol. Reprod., 2001; 65(2):628- 36]. This unique feature of bovine hyaluronidase has permitted the use of the soluble bovine testes hyaluronidase enzyme as an extract for clinical use (Wydase T M , HyalaseTM). Other PH20 species are lipid anchored enzymes that are generally not soluble without the use of detergents or lipases. For example, human PH20 is anchored to the plasma membrane via a 25 GPI anchor. Attempts to make human PH20 DNA constructs that would not introduce a lipid anchor into the polypeptide resulted in either a catalytically inactive enzyme, or an insoluble enzyme [Arming et al., Eur. J. Biochem., 1997; 247(3):810-4]. Naturally occurring macaque sperm hyaluronidase is found in both a soluble and membrane bound form. While the 64 kDa membrane bound form possesses enzyme activity at pH 7.0, the 54 kDa form is only active at 30 pH 4.0 [Cherr et al., Dev. Biol., 1996;10; 175(1): 142-53]. Thus, soluble forms of PH20 are often lacking enzyme activity under neutral conditions. 4179172_1 (GHMatters) P89111 AUA -18 As noted above and in accordance with the teachings in W02006/091871 small amounts of soluble hyaluronidase glycoproteins (sHASEGPs) can be introduced into a formulation in order to facilitate the administration of therapeutic drug into the hypodermis. By rapidly depolymerizing HA in the extracellular space sHASEGP reduces the viscosity of 5 the interstitium, thereby increasing hydraulic conductance and allowing for larger volumes to be administered safely and comfortably into the SC tissue. The increased hydraulic conductance induced by sHASEGP through reduced interstitial viscosity allows for greater dispersion, potentially increasing the systemic bioavailability of SC administered therapeutic drug. 10 When injected in the hypodermis, the depolymerization of HA by sHASEGP is localized to the injection site in the SC tissue. Experimental evidence shows that the sHASEGP is inactivated locally in the interstitial space with a half life of 13 to 20 minutes in mice, without detectable systemic absorption in blood following single intravenous dose in CD-I mice. Within the vascular compartment sHASEGP demonstrates a half life of 2.3 and 5 15 minutes in mice and Cynomolgus monkeys, respectively, with doses up to 0.5 mg/kg. The rapid clearance of sHASEGP, combined with the continual synthesis of the HA substrate in the SC tissue, results in a transient and locally-active permeation enhancement for other co injected molecules, the effects of which are fully reversible within 24 to 48 hours post administration [Bywaters G.L., et al., "Reconstitution of the dermal barrier to dye spread 20 after Hyaluronidase injection", Br. Med. J., 1951; 2 (4741): 1178-1183]. In addition to its effects on local fluid dispersion, sHASEGP also acts as absorption enhancer. Macromolecules greater than 16 kilodaltons (kDa) are largely excluded from absorption through the capillaries via diffusion and are mostly absorbed via the draining lymph nodes. A subcutaneously administered macromolecule such as e.g. a therapeutic 25 antibody (molecular weight approximately 150 kDa) must therefore traverse the interstitial matrix before reaching the draining lymphatics for subsequent absorption into the vascular compartment. By increasing local dispersion, sHASEGP increases the rate (Ka) of absorption of many macromolecules. This leads to increased peak blood levels (C..) and potentially to increased bioavailability relative to SC administration in the absence of sHASEGP 30 [Bookbinder L.H., et al., "A recombinant human enzyme for enhanced interstitial transport of therapeutics", J. Control. Release 2006; 114: 230-241]. 4179172.1 (GHMatters) P89111.AU.1 -19 Hyaluronidase products of animal origin have been used clinically for over 60 years, primarily to increase the dispersion and absorption of other co-administered drugs and for hypodermoclysis (SC injection/infusion of fluid in large volume) [Frost G.I., "Recombinant human hyaluronidase (rHuPH20): an enabling platform for subcutaneous drug and fluid 5 administration", Expert Opinion on Drug Delivery, 2007; 4: 427-440]. The details on the mechanism of action of hyaluronidases have been described in detail in the following publications: Duran-Reynolds F., "A spreading factor in certain snake venoms and its relation to their mode of action", CR Soc Biol Paris, 1938; 69-8 1; Chain E., "A mucolytic enzyme in testes extracts", Nature 1939; 977-978; Weissmann B., "The transglycosylative action of 10 testicular hyaluronidase", J. Biol. Chem., 1955; 216: 783-94; Tammi, R., Saamanen, A.M., Maibach, H.I., Tammi M., "Degradation of newly synthesized high molecular mass hyaluronan in the epidermal and dermal compartments of human skin in organ culture", J. Invest. Dermatol. 1991; 97:126-130; Laurent, U.B.G., Dahl, L.B., Reed, R.K., "Catabolism of hyaluronan in rabbit skin takes place locally, in lymph nodes and liver", Exp. Physiol. 15 1991; 76: 695-703; Laurent, T.C. and Fraser, J.R.E., "Degradation of Bioactive Substances: Physiology and Pathophysiology", Henriksen, J.H. (Ed) CRC Press, Boca Raton, FL; 1991. pp. 249-265; Harris, E.N., et al., "Endocytic function, glycosaminoglycan specificity, and antibody sensitivity of the recombinant human 190-kDa hyaluronan receptor for endocytosis (HARE)", J. Biol. Chem. 2004; 279:36201-36209; Frost, G.I., "Recombinant human 20 hyaluronidase (rHuPH20): an enabling platform for subcutaneous drug and fluid administration", Expert Opinion on Drug Delivery, 2007; 4: 427-440. Hyaluronidase products approved in EU countries include Hylase@ "Dessau" and Hyalase@. Hyaluronidase products of animal origin approved in the US include VitraseTM, HydaseTM, and AmphadaseTM. 25 The safety and efficacy of hyaluronidase products have been widely established. The most significant safety risk identified is hypersensitivity and/or allergenicity, which is thought to be related to the lack of purity of the animal-derived preparations [Frost, G.I., "Recombinant human hyaluronidase (rHuPH20): an enabling platform for subcutaneous drug and fluid administration", Expert Opinion on Drug Delivery, 2007; 4 : 427-440]. It should be 30 noted that there are differences with respect to the approved dosages of animal-derived hyaluronidases between the UK, Germany and the US. In the UK, the usual dose as an adjuvant to subcutaneous or intramuscular injection is 1500 units, added directly to the injection. In the US, the usual dose used for this purpose is 150 units. In hypodermoclysis, 41791721 (GHMatters) P8911 1.AU-1 -20 hyaluronidase is used to aid the subcutaneous administration of relatively large volumes of fluids. In the UK, 1500 units of hyaluronidase are generally given with each 500 to 1000 ml of fluid for subcutaneous use. In the US, 150 units are considered adequate for each liter of hypodermoclysis solution. In Germany, 150 to 300 units are considered adequate for this 5 purpose. In the UK, the diffusion of local anesthetics is accelerated by the addition of 1500 units. In Germany and the US 150 units are considered adequate for this purpose. The dosage differences notwithstanding (the dosage in the UK is ten times higher than in the US), no apparent differences in the safety profiles of animal-derived hyaluronidase products marketed in the US and UK, respectively, have been reported. 10 On December 2, 2005, Halozyme Therapeutics Inc. received approval from the FDA for an injectable formulation of the recombinant human hyaluronidase, rHuPH20 (HYLENEXTM). The FDA approved HYLENEXTM at a dose of 150 units for SC administration of the following indications: - as an adjuvant to increase the absorption and dispersion of other injected drugs 15 - for hypodermoclysis - as an adjunct in SC urography for improving resorption of radiopaque agents. As part of that regulatory review it was established that rHuPH20 possesses the same properties of enhancing the dispersion and absorption of other injected drugs as the previously approved animal-derived hyaluronidase preparations, but with an improved safety 20 profile. In particular, the use of recombinant human hyaluronidase (rHuPH20) compared with animal-derived hyaluronidases minimizes the potential risk of contamination with animal pathogens and transmissible spongiform encephalopathies. Soluble Hyaloronidase glycoproteins (sHASEGP), a process for preparing the same and their use in pharmaceutical compositions have been described in WO 2004/078140. The use 25 of soluble Hyaloronidase glycoproteins in combination with variety of exemplary antibodies, such as e.g. Trastuzumab, has been mentioned in WO 2006/091871. The detailed experimental work as outlined further below has shown that the formulations of the present invention surprisingly have favorable storage stability and fulfill all necessary requirements for approval by the health authorities. 41791721 (GHMaIers) P891 11.AU.1 -21 The hyaluronidase enzyme in the formulations of the present invention enhances the delivery of the anti-HER2 antibody to the systemic circulation, e.g. by increasing the absorption of the active substance (it acts as a permeation enhancer). The hyaluronidase enzyme also increases the delivery of the therapeutic anti-HER2 antibody into the systemic 5 circulation via the subcutaneous application route by the reversible hydrolyzation of hyaluronan, an extracellular component of the SC interstitial tissue. The hydrolysis of hyaluronan in the hypodermis temporarily opens channels in the interstitial space of the SC tissue and thereby improves the delivery of the therapeutic anti-HER2 antibody into the systemic circulation. In addition, the administration shows reduced pain in humans and less 10 volume-derived swelling of the SC tissue. Hyaluronidase, when administered locally has its entire effect locally. In other word hyaluronidase is inactivated and metabolized locally in minutes and has not been noted to have systemic or long term effects. The rapid inactivation of hyaluronidase within minutes when it enters the blood stream precludes a realistic ability to perform comparable 15 biodistribution studies between different hyaluronidase products. This property also minimizes any potential systemic safety concerns because the hyaluronidase product cannot act at distant sites. The unifying feature of all hyaluronidase enzymes is their ability to depolymerize hyaluronan, regardless of differences in chemical structure, in species source, in tissue 20 sources, or in the batches of drug product sourced from the same species and tissue. They are unusual in that their activity is the same (except for potency) in spite of having different structures. The hyaluronidase enzyme excipient in accordance with the formulation of the present invention is characterized by having no adverse effect on the molecular integrity of the anti 25 HER2 antibody in the stable pharmaceutical formulation described herein. Furthermore, the hyaluronidase enzyme merely modifies the delivery of the anti-HER2 antibody to the systemic circulation but does not possess any properties that could provide or contribute to the therapeutic effects of systemically absorbed anti-HER2 antibody. The hyaluronidase enzyme is not systemically bioavailable and does not adversely affect the molecular integrity 30 of the anti-HER2 antibody at the recommended storage conditions of the stable pharmaceutical formulation in accordance with the invention. It is therefore to be considered as an excipient in the anti-HER2 antibody formulation in accordance with this invention. As 41917291 (GHMattems) P6911tAU.1 -22 it exerts no therapeutic effect it represents a constituent of the pharmaceutical form apart from the therapeutically active anti-HER2 antibody. A number of suitable hyaluronidase enzymes in accordance with the present invention are known from the prior art. The preferred enzyme is a human hyaluronidase enzyme, most 5 preferably the enzyme known as rHuPH20. rHuPH20 is a member of the family of neutral and acid-active 0-1,4 glycosyl hydrolases that depolymerize hyaluronan by the hydrolysis of the P-1,4 linkage between the C, position of N-acetyl glucosamine and the C 4 position of glucuronic acid. Hyaluronan is a polysaccharide found in the intracellular ground substance of connective tissue, such as the subcutaneous interstitial tissue, and of certain specialized 10 tissues, such as the umbilical cord and vitreous humor. The hydrolysis of hyaluronan temporarily decreases the viscosity of the interstitial tissue and promotes the dispersion of injected fluids or of localized transudates or exudates, thus facilitating their absorption. The effects of hyaluronidase are local and reversible with complete reconstitution of the tissue hyaluronan occurring within 24 to 48 hours [Frost, G.I., "Recombinant human hyaluronidase 15 (rHuPH20): an enabling platform for subcutaneous drug and fluid administration", Expert Opinion on Drug Delivery, 2007; 4:427-440]. The increase in the permeability of connective tissue through the hydrolysis of hyaluronan correlates with the efficacy of hyaluronidase for their capability to increase the dispersion and absorption of co-administered molecules. The human genome contains several hyaluronidase genes. Only the PH20 gene product 20 possesses effective hyaluronidase activity under physiologic extracellular conditions and acts as a spreading agent, whereas acid-active hyaluronidases do not have this property. rHuPH20 is the first and only recombinant human hyaluronidase enzyme currently available for therapeutic use. Naturally occurring human PH20 protein has a lipid anchor attached to the carboxy terminal amino acid that anchors it to the plasma membrane. The 25 rHuPH20 enzyme developed by Halozyme is a truncated deletion variant that lacks such amino acids in the carboxy terminus responsible for the lipid attachment. This gives rise to a soluble, neutral pH-active enzyme similar to the protein found in bovine testes preparations. The rHuPH20 protein is synthesized with a 35 amino acid signal peptide that is removed from the N-terminus during the process of secretion. The mature rHuPH20 protein contains 30 an authentic N-terminal amino acid sequence orthologous to that found in some bovine hyaluronidase preparations. 41791721 (GHMatters) P89111.AU.1 -23 The PH20 hyaluronidases, including the animal derived PH20 and recombinant human rHuPH20, depolymerize hyaluronan by the hydrolysis of the P-1,4 linkage between the C 1 position of N-acetyl glucosamine and the C 4 position of glucuronic acid. The tetrasaccharide is the smallest digestion product [Weissmann, B., "The transglycosylative action of testicular 5 hyaluronidase", J. Biol. Chem., 1955; 216: 783-94]. This N-acetyl glucosamine/glucuronic acid structure is not found in N-linked glycans of recombinant biological products and therefore rHuPH20 will not affect the glycosylation of antibodies it is formulated with, such as e.g. Trastuzumab. The rHuPH20 enzyme itself possesses six N-linked glycans per molecule with core structures similar to that found in monoclonal antibodies. As anticipated, 10 these N-linked structures do not change over time, confirming the lack of enzymatic activity of rHuPH20 on these N-linked glycan structures. The short half life of rHuPH20 and the constant synthesis of hyaluronan lead to a short and local action of the enzyme on tissues. The hyaluronidase enzyme which is an excipient in the subcutaneous formulation in accordance with the present invention can be prepared by using recombinant DNA 15 technology. In this way it is ensured that the same protein (identical amino acid sequence) is obtained all the time and that an allergic reaction, e.g. caused by contaminating proteins co purified during extraction from a tissue, is avoided. The hyaluronidase enzyme used in the formulation as exemplified herein is a human enzyme, viz. rHuPH20. The amino acid sequence of rHuPH20 (HYLENEX

TM

) is well known and available 20 under CAS Registry No. 75971-58-7. The approximate molecular weight is 61 kDa. Multiple structural and functional comparisons have been performed between naturally sourced mammalian hyaluronidase and PH-20 cDNA clones from humans and other mammals. The PH-20 gene is the gene used for the recombinant product rHuPH20; however the recombinant drug product is a 447 amino acid truncated version of the full protein 25 encoded by the PH-20 gene. Structural similarities with respect to amino acid sequences rarely exceed 60% in any comparison. Functional comparisons show that the activity of rHuPH20 is very similar to that of previously approved hyaluronidase products. This information is consistent with the clinical findings during the past 50 years that regardless of the source of the hyaluronidase, the clinical safety and efficacy of units of hyaluronidase are 30 equivalent. 41791721 (GHMatters) P8911tAU.1 -24 The use of rHuPH20 in the anti-HER2 antibody SC formulation in accordance with the present disclosure allows the administration of higher volumes of drug product and to potentially enhance the absorption of subcutaneously administered Trastuzumab into the systemic circulation. 5 The osmolality of the stable pharmaceutical formulation in accordance with the disclosure is 330 ± 50 mOsm/kg. The stable pharmaceutical formulation is essentially free from visible (human eye inspection) particles. The sub-visible particles (as measured by light obscuration) should fulfill the following criteria: 10 - maximum number of particles > 10pm per vial -> 6000 - maximum number of particles > 25pim per vial -> 600 Also disclosed is use of a formulation for the preparation of a medicament useful for treating a disease or disorder amenable to treatment with an anti-HER2 antibody such as e.g. cancer or a non-malignant disease in a subject comprising administering the formulation 15 described herein to a subject in an amount effective to treat the said disease or disorder. The anti-HER2 antibody can be co-administered concomitantly or sequentially with a chemotherapeutic agent. Also disclosed is a method of treating a disease or disorder which is amenable to treatment with an anti-HER2 antibody (e.g. cancer or a non-malignant disease) in a subject 20 comprising administering the formulation described herein to a subject in an amount effective to treat the said disease or disorder. The cancer or a non-malignant disease will generally involve HER2-expressing cells, such that the HER2 antibody in the therapeutic pharmaceutical SC formulation in accordance with the present invention is able to bind to the affected cells. Various cancer or a non-malignant diseases that can be treated with a 25 formulation in accordance with the present disclosure are listed in the definitions section further below. The stable pharmaceutical formulation of the pharmaceutically active anti-HER2 antibody can be administered as subcutaneous injection, whereby the administration is repeated several times with time intervals of 3 weeks (q3w). 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 -25 The full volume of the injection fluid is in most case administered within a time period of 1 to 10 minutes, preferably 2 to 6 minutes, most preferably 3 ± 1 minutes. In adjuvant EBC patients and amongst patients with MBC receiving Trastuzumab monotherapy, where no other intravenous (IV) chemotherapeutic agents are given, such subcutaneous administration 5 leads to increased patient convenience with the potential for self- administration at home. This leads to improved compliance and reduces / eliminates costs associated with IV administration (viz., nursing costs for IV administration, rental of day-beds, patient travel etc). Subcutaneous administration in accordance with the present invention will most likely be associated with a reduced frequency and / or intensity of infusion-related reactions. 10 The addition of the hyaluronidase to the formulation allows increasing the injection volume which can be safely and comfortably administered subcutaneously. Under normal circumstances the injection volume is 1 to 15 ml. It has been observed that the administration of the formulation in accordance with the present invention increases the dispersion, absorption and the bioavailability of the therapeutic antibody. Large molecules (i.e. > 16 kDa) 15 that are administered via the SC route are preferentially absorbed into the vascular compartment through the draining lymphatic fluids [Supersaxo, A., et al., "Effect of Molecular Weight on the Lymphatic Absorption of Water-Soluble Compounds Following Subcutaneous Administration", 1990; 2:167-169; Swartz, M. A., "Advanced Drug Delivery Review, The physiology of the lymphatic system", 2001; 50: 3-20]. The rate of introduction 20 of these large molecules into the systemic circulation is thus slowed relative to intravenous infusion, therefore potentially resulting in reduced frequency/intensity of infusion related reactions. The production of the subcutaneous Trastuzumab formulation in accordance with the invention requires high antibody concentrations (approx. 120 mg/ml) in the final step of 25 purification of the manufacturing process. Therefore an additional process step (ultrafiltration/diafiltration) is added to the conventional manufacturing process of Trastuzumab. In accordance with the teachings in WO 97/04801 the highly concentrated, stable pharmaceutical anti-HER2 antibody formulation in accordance with the present invention can also be provided as stabilized protein formulation which can reconstituted with 30 a suitable diluent to generate a high anti-HER2 antibody concentration reconstituted formulation. 417917L2_ (GHMatters) P8911iAU.i -26 The HER2 antibody SC formulation in accordance with this invention is mainly used to treat cancer. Whereby the terms "cancer" and "cancerous" refer to or describe the physiological condition in mammals that is typically characterized by unregulated cell growth. Examples of cancer include, but are not limited to, carcinoma, lymphoma, blastoma 5 (including medulloblastoma and retinoblastoma), sarcoma (including liposarcoma and synovial cell sarcoma), neuroendocrine tumors (including carcinoid tumors, gastrinoma and islet cell cancer), mesothelioma, schwannoma (including acoustic neuroma), meningioma, adenocarcinoma, melanoma, and leukemia or lymphoid malignancies. More particular examples of such cancers include squamous cell cancer (e.g. epithelial squamous cell cancer), 10 lung cancer including small-cell lung cancer, non- small cell lung cancer, adenocarcinoma of the lung and squamous carcinoma of the lung, cancer of the peritoneum, hepatocellular cancer, gastric or stomach cancer including gastrointestinal cancer, pancreatic cancer, glioblastoma, cervical cancer, ovarian cancer, liver cancer, bladder cancer, hepatoma, breast cancer, colon cancer, rectal cancer, colorectal cancer, endometrial or uterine carcinoma, 15 salivary gland carcinoma, kidney or renal cancer, prostate cancer, vulval cancer, thyroid cancer, hepatic carcinoma, anal carcinoma, penile carcinoma, testicular cancer, esophageal cancer, tumors of the biliary tract, as well as head and neck cancer. In the claims which follow and in the description of the invention, except where the context requires otherwise due to express language or necessary implication, the word 20 "comprise" or variations such as "comprises" or "comprising" is used in an inclusive sense, i.e. to specify the presence of the stated features but not to preclude the presence or addition of further features in various embodiments of the invention. The term "about" as used in the present patent specification is meant to specify that the specific value provided may vary to a certain extent, such as e.g. means that variations in the 25 range of± 10 %, preferably ± 5 %, most preferably ± 2 % are included in the given value. A cancer which "overexpresses" a HER receptor is one which has significantly higher levels of a HER receptor, such as HER2, at the cell surface thereof, compared to a noncancerous cell of the same tissue type. Such overexpression may be caused by gene amplification or by increased transcription or translation. HER receptor overexpression may 30 be determined in a diagnostic or prognostic assay by evaluating increased levels of the HER protein present on the surface of a cell (e.g. via an immunohistochemistry assay; IHC). Alternatively, or additionally, one may measure levels of HER-encoding nucleic acid in the 4179172_1 (GHMatters) P891 11.AU.1 -27 cell, e.g. via fluorescent in situ hybridization (FISH; see W098/45479), Southern blotting, or polymerase chain reaction (PCR) techniques, such as real time quantitative PCR (RT-PCR). One may also study HER receptor overexpression by measuring shed antigen (e.g., HER extracellular domain) in a biological fluid such as serum [see, e.g., U.S. Patent No. 4,933,294 5 issued June 12, 1990; W091/05264 published April 18, 1991; U.S. Patent 5,401,638 issued March 28, 1995; and Sias et al., J. Immunol. Methods 1990; 132: 73-80]. Aside from the above assays, various in vivo assays are available to the skilled practitioner. For example, one may expose cells within the body of the patient to an antibody which is optionally labeled with a detectable label, e.g. a radioactive isotope, and binding of the antibody to cells 10 in the patient can be evaluated, e.g. by external scanning for radioactivity or by analyzing a biopsy taken from a patient previously exposed to the antibody. Conversely, a cancer which "does not overexpress HER2 receptor" is one which does not express higher than normal levels of HER2 receptor compared to a noncancerous cell of the same tissue type. 15 A cancer which "overexpresses" a HER ligand is one which produces significantly higher levels of that ligand compared to a noncancerous cell of the same tissue type. Such overexpression may be caused by gene amplification or by increased transcription or translation. Overexpression of the HER ligand may be determined diagnostically by evaluating levels of the ligand (or nucleic acid encoding it) in the patient, e.g. in a tumor 20 biopsy or by various diagnostic assays such as the IHC, FISH, southern blotting, PCR or in vivo assays well known in the art. It is contemplated that the HER2 antibody SC formulation in accordance with this invention may also be used to treat various non-malignant diseases or disorders, such a include autoimmune disease (e.g. psoriasis); endometriosis; scleroderma; restenosis; polyps 25 such as colon polyps, nasal polyps or gastrointestinal polyps; fibroadenoma; respiratory disease; cholecystitis; neurofibromatosis; polycystic kidney disease; inflammatory diseases; skin disorders including psoriasis and dermatitis; vascular disease; conditions involving abnormal proliferation of vascular epithelial cells; gastrointestinal ulcers; Menetrier's disease, secreting adenomas or protein loss syndrome; renal disorders; angiogenic disorders; ocular 30 disease such as age related macular degeneration, presumed ocular histoplasmosis syndrome, retinal neovascularization from proliferative diabetic retinopathy, retinal vascularization, diabetic retinopathy, or age related macular degeneration; bone associated pathologies such 4170172_ (GHMOtters) P8911 1AUA1 -28 as osteoarthritis, rickets and osteoporosis; damage following a cerebral ischemic event; fibrotic or edemia diseases such as hepatic cirrhosis, lung fibrosis, carcoidosis, throiditis, hyperviscosity syndrome systemic, Osier Weber-Rendu disease, chronic occlusive pulmonary disease, or edema following bums, trauma, radiation, stroke, hypoxia or ischemia; 5 hypersensitivity reaction of the skin; diabetic retinopathy and diabetic nephropathy; Guillain Barre syndrome; graft versus host disease or transplant rejection; Paget' s disease; bone or joint inflammation; photoaging (e.g. caused by UV radiation of human skin); benign prostatic hypertrophy; certain microbial infections including microbial pathogens selected from adenovirus, hantaviruses, Borrelia burgdorferi, Yersinia spp. and Bordetella pertussis; 10 thrombus caused by platelet aggregation; reproductive conditions such as endometriosis, ovarian hyperstimulation syndrome, preeclampsia, dysfunctional uterine bleeding, or menometrorrhagia; synovitis; atheroma; acute and chronic nephropathies (including proliferative glomerulonephritis and diabetes-induced renal disease); eczema; hypertrophic scar formation; endotoxic shock and fungal infection; familial adenomatosis polyposis; 15 neurodedenerative diseases (e.g. Alzheimer's disease, AIDS-related dementia, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, spinal muscular atrophy and cerebellar degeneration); myelodysplastic syndromes; aplastic anemia; ischemic injury; fibrosis of the lung, kidney or liver; T-cell mediated hypersensitivity disease; infantile hypertrophic pyloric stenosis; urinary obstructive syndrome; psoriatic arthritis; and 20 Hasimoto's thyroiditis. Exemplary non-malignant indications for therapy herein include psoriasis, endometriosis, scleroderma, vascular disease (e.g. restenosis, artherosclerosis, coronary artery disease, or hypertension), colon polyps, fibroadenoma or respiratory disease (e.g. asthma, chronic bronchitis, bronchieactasis or cystic fibrosis). Where the indication is cancer, the patient may be treated with a combination of the 25 antibody formulation, and a chemotherapeutic agent. The combined administration includes co-administration or concurrent administration, using separate formulations or a single pharmaceutical formulation, and consecutive administration in either order, wherein preferably there is a time period while both (or all) active agents simultaneously exert their biological activities. Thus, the chemotherapeutic agent may be administered prior to, or 30 following, administration of the antibody formulation in accordance with the present invention. In this embodiment, the timing between at least one administration of the chemotherapeutic agent and at least one administration of the antibody formulation in accordance with the present invention is preferably approximately 1 month or less, and most 4179172J (GHMaIers) P89111.AU.1 -29 preferably approximately 2 weeks or less. Alternatively, the chemotherapeutic agent and the antibody formulation in accordance with the present invention are administered concurrently to the patient, in a single formulation or separate formulations. Treatment with the said antibody formulation will result in an improvement in the signs 5 or symptoms of cancer or disease. For instance, where the disease being treated is cancer, such therapy may result in an improvement in survival (overall survival and/or progression free survival) and / or may result in an objective clinical response (partial or complete). Moreover, treatment with the combination of the chemotherapeutic agent and the antibody formulation may result in a synergistic or greater than additive, therapeutic benefit to the 10 patient. Normally the antibody in the formulation administered is a naked antibody. However, the antibody administered may be conjugated with a cytotoxic agent. The immunoconjugate and/or antigen to which it is bound is / are then internalized by the cell, resulting in increased therapeutic efficacy of the immunoconjugate in killing the cancer cell to which it binds. In 15 one embodiment, the cytotoxic agent targets or interferes with nucleic acid in the cancer cell. Examples of such cytotoxic agents include maytansinoids, calioheamicins, ribonucleases and DNA endonucleases. The clinically most advanced immunoconjugates are Trastuzumab maytansinoid immunoconjugates (T-DM1) as they are described in WO 2003/037992, in particular the immunoconjugate T-MCC-DM1, the chemical name of which is N 2 -deacetyl 20 N 2 '-(3-mercapto-1-oxopropyl)-maytansine-4-maleimidomethyl-cyclohexyl-1-carboxyl Trastuzumab. For subcutaneous delivery, the formulation may be administered via a suitable device, such as (but not limited to) a syringe; an injection device (e.g. the INJECT-EASETM and GENJECTTM device); an infusion pump (such as e.g. Accu-ChekTM); an injector pen (such as 25 the GENPENTM; an needleless device (e.g. MEDDECTORTM and BIOJECTORTM); or via a subcutaneous patch delivery system. A suitable delivery system for the formulations in accordance with the present invention is described in WO 2010/029054. Such device comprises about 5 to about 15 ml or more particularly 5 ml of the liquid formulation in accordance with the present invention. 30 For the prevention or treatment of disease, the appropriate dosage of the antibody will depend on the type of disease to be treated, as defined above, the severity and course of the 41791721 (GHMatters) P891 11AU.1 -30 disease, whether the antibody is administered for preventive or therapeutic purposes, on the previous therapy, the patient's clinical history and his response to the antibody, and the discretion of the attending physician. The antibody is suitably administered to the patient at one time or over a series of treatments. Depending on the type and severity of the disease, 5 about 1 pg/kg to 50 mg/kg of bodyweight or more specifically between about 0.1 mg/kg to 20 mg/kg of bodyweight) of the anti-HER2 antibody is a candidate initial dosage for administration to the patient, whether, for example, by one or more separate administrations, or by continuous infusion. More specifically the dosage of the antibody will be in the range from about 0.05 mg anti-HER2 antibody / kg of bodyweight to about 10 mg anti-HER2 10 antibody / kg of bodyweight. If a chemotherapeutic agent is administered, it is usually administered at dosages known therefore, or optionally lowered due to combined action of the drugs or negative side effects attributable to administration of the chemotherapeutic agent. Preparation and dosing schedules for such chemotherapeutic agents may be used according to manufacturers' instructions or as determined empirically by the skilled practitioner. 15 Preparation and dosing schedules for such chemotherapy are also described in Chemotherapy Service Ed., M.C. Perry, Williams & Wilkins, Baltimore, MD (1992). Other therapeutic regimens may be combined with the antibody including, but not limited to a second (third, fourth, etc) chemotherapeutic agent(s) (in another word a "cocktail" of different chemotherapeutic agents); another monoclonal antibody; a growth 20 inhibitory agent; a cytotoxic agent; a chemotherapeutic agent; a EGFR-targeted drug; a tyrosine kinase inhibitor; an anti-angiogenic agent; and/or cytokine, etc.; or any suitable combination thereof In addition to the above therapeutic regimes, the patient may be subjected to surgical removal of cancer cells and/or radiation therapy. 25 In another embodiment of the invention, an article of manufacture is provided which contains the pharmaceutical formulation of the present invention and provides instructions for its use. This article of manufacture comprises a container. Suitable containers include, for example, bottles, vials (e.g. multiple or dual chamber vials), syringes (such as multiple or dual chamber syringes) and test tubes. The container may be formed from a variety of 30 materials such as glass or plastic. The container holds the formulation and the label on, or associated with, the container may indicate directions for use. The container holding the 4179172_1 (GHMatters) P891 11.AU.1 -31 formulation may be a multi-use vial, which allows for repeat administrations (e.g. from 2 to 6 administrations) of the reconstituted formulation. The article of manufacture may further include other materials desirable from a commercial and user standpoint, including other buffers, diluents, filters, needles, syringes, and package inserts with instructions for use. 5 The term "pharmaceutical formulation" refers to a preparation which is in such form as to permit the biological activity of the active ingredient to be effective, and which contains no additional components which are unacceptably toxic to a subject to which the formulation would be administered. Such formulations are sterile. A "sterile" formulation is aseptic or free from all living microorganisms and their 10 spores. A "stable" formulation is one in which all the protein therein essentially retain their physical stability and/or chemical stability and/or biological activity upon storage at the intended storage temperature, e.g. 2 - 8 0 C. It is desired that the formulation essentially retains its physical and chemical stability, as well as its biological activity upon storage. The 15 storage period is generally selected based on the intended shelf-life of the formulation. Furthermore, the formulation should be stable following freezing (to, e.g., -70 C) and thawing of the formulation, for example following 1, 2 or 3 cycles of freezing and thawing. Various analytical techniques for measuring protein stability are available in the art and are reviewed in Peptide and Protein Drug Delivery, 247-301, Vincent Lee Ed., Marcel Dekker, 20 Inc., New York, New York, Pubs. (1991) and Jones, A. Adv. Drug Delivery Rev. 10: 29-90 (1993), for example. Stability can be measured at a selected temperature for a selected time period. Stability can be evaluated qualitatively and/or quantitatively in a variety of different ways, including evaluation of aggregate formation (for example using size exclusion chromatography, by measuring turbidity, and/or by visual inspection); by assessing charge 25 heterogeneity using cation exchange chromatography or capillary zone electrophoresis; amino-terminal or carboxy-terminal sequence analysis; mass spectrometric analysis; SDS PAGE analysis to compare reduced and intact antibody; peptide map (for example tryptic or LYS-C) analysis; evaluating biological activity or antigen binding function of the antibody; etc. Instability may involve any one or more of: aggregation, deamidation (e.g. Asn 30 deamidation), oxidation (e.g. Met oxidation), isomerization (e.g. Asp isomeriation), clipping/hydrolysis/fragmentation (e.g. hinge region fragmentation), succinimide formation, unpaired cysteine(s), N-terminal extension, C-terminal processing, glycosylation changes, etc. 4179172_1 (GHMatters) P8911.AU.1 -32 A "deamidated" monoclonal antibody herein is one in which one or more asparagine residue thereof has been modified, e.g. to an aspartic acid or an iso-aspartic acid by a post translational modification. As used herein the term "buffering agent providing a pH of 5.5 ± 2.0" refers to an agent 5 which provides that the solution comprising it resists changes in pH by the action of its acid/base conjugate components. The buffer used in the formulations in accordance with the present invention has a pH in the range from about 5.0 to about 7.0, or from about 5.0 to about 6.5, or from about 5.3 to about 5.8. A pH of about 5.5 has to be found to be most suitable. Examples of buffering agents that will control the pH in this range include acetate, 10 succinate, gluconate, histidine, citrate, glycylglycine and other organic acid buffers. The most suitable buffer in accordance with the present invention is a histidine buffer, such as e.g. L histidine/HCl. A "histidine buffer" is a buffer comprising the amino acid histidine. Examples of histidine buffers include histidine chloride, histidine acetate, histidine phosphate, histidine 15 sulfate. The histidine buffer identified in the examples as being most suitable is a histidine chloride buffer. Such histidine chloride buffer is prepared by titrating L-histidine (free base, solid) with diluted hydrochloric acid. In particular the histidine buffer or histidine chloride buffer is at pH of 5.5 ± 0.6, more particularly at a pH from about 5.3 to about 5.8, and most particularly has a pH of 5.5. 20 By "isotonic" is meant that the formulation of interest has essentially the same osmotic pressure as human blood. Isotonic formulations will generally have an osmotic pressure from about 250 to 350 mOsm. Isotonicity can be measured using a vapor pressure or freezing point depression type osmometer. A "saccharide" herein comprises the general composition (CH 2 0). and derivatives 25 thereof, including monosaccharides, disaccharides, trisaccharides, polysaccharides, sugar alcohols, reducing sugars, nonreducing sugars, etc. Examples of saccharides herein include glucose, sucrose, trehalose, lactose, fructose, maltose, dextran, glycerin, dextran, erythritol, glycerol, arabitol, sylitol, sorbitol, mannitol, mellibiose, melezitose, raffinose, mannotriose, stachyose, maltose, lactulose, maltulose, glucitol, maltitol, lactitol, iso-maltulose, etc. 30 Particularly the formulations described herein comprise a non-reducing disaccharide as a 4179172_1 (GHMattors) P8911.I AUA -33 stabilizing agent, such as a saccharide selected from the group of trehalose (e.g. in the form of a,a-trehalose dihydrate) and sucrose. Herein, a "surfactant" refers to a surface-active agent, e.g. a nonionic surfactant. Examples of surfactants herein include polysorbate (for example, polysorbate 20 and, 5 polysorbate 80); poloxamer (e.g. poloxamer 188); Triton; sodium dodecyl sulfate (SDS); sodium laurel sulfate; sodium octyl glycoside; lauryl-, myristyl-, linoleyl-, or stearyl sulfobetaine; lauryl-, myristyl-, linoleyl- or stearyl-sarcosine; linoleyl-, myristyl-, or cetyl betaine; lauroamidopropyl-, cocamidopropyl-, linoleamidopropyl-, myristamidopropyl-, palmidopropyl-, or isostearamidopropyl-betaine (e.g. lauroamidopropyl); myristamidopropyl-, 10 palmidopropyl-, or isostearamidopropyl-dimethylamine; sodium methyl cocoyl-, or disodium methyl oleyl-taurate; and the MONAQU ATTM series (Mona Industries, Inc., Paterson, New Jersey); polyethyl glycol, polypropyl glycol, and copolymers of ethylene and propylene glycol (e.g. Pluronics, PF68 etc); etc. Polysorbate 20 (PS20) and Polysorbate 80 (PS80), respectively have been found to be particularly suitable in the formulations described herein. 15 The term "antibody" herein is used in the broadest sense and specifically covers full length monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g. bispecific antibodies) formed from at least two full length antibodies, and antibody fragments, so long as they exhibit the desired biological activity. The term "monoclonal antibody" as used herein refers to an antibody obtained from a 20 population of substantially homogeneous antibodies, i.e., the individual antibodies comprising the population are identical and/or bind the same epitope, except for possible variants that may arise during production of the monoclonal antibody, such variants generally being present in minor amounts. In contrast to polyclonal antibody preparations that typically include different antibodies directed against different determinants (epitopes), each 25 monoclonal antibody is directed against a single determinant on the antigen. In addition to their specificity, the monoclonal antibodies are advantageous in that they are uncontaminated by other immunoglobulins. The modifier "monoclonal" indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not to be construed as requiring production of the antibody by any particular method. For 30 example, the monoclonal antibodies to be used in accordance with the present invention may be made by the hybridoma method first described by Kdhler et al, Nature, 256:495 (1975), or may be made by recombinant DNA methods (see, e.g., U.S. Patent No. 4,816,567). The 4179172_1 (GHMaUers) P89111.AU.1 -34 "monoclonal antibodies" may also be isolated from phage antibody libraries using the techniques described in Clarkson et al., Nature, 352:624-628 (1991) and Marks et al., J. Mol. Biol., 222:581-597 (1991). An "antibody fragment" comprises a portion of a full length antibody, in particular 5 comprises the antigen-binding or variable region thereof Examples of antibody fragments include Fab, Fab', F(ab') 2 , and Fv fragments; diabodies; linear antibodies; single-chain antibody molecules; and multispecific antibodies formed from antibody fragment(s). A "full length antibody" is one which comprises an antigen-binding variable region as well as a light chain constant domain (CL) and heavy chain constant domains, CH1, CH2 and 10 CH3. The constant domains may be native sequence constant domains (e.g. human native sequence constant domains) or amino acid sequence variants thereof. In particular the full length antibody has one or more effector functions. An "amino acid sequence variant" antibody herein is an antibody with an amino acid sequence which differs from a main species antibody. Ordinarily, amino acid sequence 15 variants will possess at least about 70% homology with the main species antibody, and preferably, they will be at least about 80%, more preferably at least about 90% homologous with the main species antibody. The amino acid sequence variants possess substitutions, deletions, and/or additions at certain positions within or adjacent to the amino acid sequence of the main species antibody. Examples of amino acid sequence variants herein include acidic 20 variant (e.g. deamidated antibody variant), basic variant, the antibody with an amino-terminal leader extension (e.g. VHS-) on one or two light chains thereof, antibody with a C-terminal lysine residue on one or two heavy chains thereof, etc, and includes combinations of variations to the amino acid sequences of heavy and/or light chains. The antibody variant of particular interest herein is the antibody comprising an amino-terminal leader extension on 25 one or two light chains thereof, optionally further comprising other amino acid sequence and/or glycosylation differences relative to the main species antibody. A "glycosylation variant" antibody herein is an antibody with one or more carbohydrate moieties attached thereto which differ from one or more carbohydrate moieties attached to a main species antibody. Examples of glycosylation variants herein include antibody with a G1 30 or G2 oligosaccharide structure, instead a GO oligosaccharide structure, attached to an Fc region thereof, antibody with one or two carbohydrate moieties attached to one or two light 4179172_1 (GHMattem) P891 1tAU.1 -35 chains thereof, antibody with no carbohydrate attached to one or two heavy chains of the antibody, etc, and combinations of glycosylation alterations. Moreover the term "glycosylation variant" includes also glycoengineered antibodies such as those described in EP 1'331'266 and USP 7'517'670. 5 Antibody "effector functions" refer to those biological activities attributable to the Fc region (a native sequence Fe region or amino acid sequence variant Fc region) of an antibody. Examples of antibody effector finctions include C Iq binding; complement dependent cytotoxicity (CDC); Fc receptor binding; antibody-dependent cell-mediated cytotoxicity (ADCC); phagocytosis; down regulation of cell surface receptors (e.g. B cell receptor; BCR), 10 etc. Depending on the amino acid sequence of the constant domain of their heavy chains, full length antibodies can be assigned to different "classes". There are five major classes of full length antibodies: IgA, IgD, IgE, IgG, and IgM, and several of these may be further divided into subclassess" (isotypes), e.g., IgGl, IgG2, IgG3, IgG4, IgA, and IgA2. The heavy 15 chain constant domains that correspond to the different classes of antibodies are called a [alpha], 8 [delta], e [epsilon], y [gamma], and p. [mu], respectively. The subunit structures and three-dimensional configurations of different classes of immunoglobulins are well known. Herein, "biological activity" of a monoclonal antibody refers to the ability of the antibody to bind to antigen and result in a measurable biological response which can be 20 measured in vitro or in vivo. Such activity may be antagonistic (for example where the antibody is a HER2 antibody) or agonistic. In the case of Pertuzumab, in one embodiment, the biological activity refers to the ability of the formulated antibody to inhibit proliferation of the human breast cancer cell line MDA-MB-175-VII. The term "monoclonal antibodies" herein specifically include the so-called chimeric 25 antibodies in which a portion of the heavy and/or light chain is identical with or homologous to corresponding sequences in antibodies derived from a particular species or belonging to a particular antibody class or subclass, while the remainder of the chain(s) is identical with or homologous to corresponding sequences in antibodies derived from another species or belonging to another antibody class or subclass, as well as fragments of such antibodies, so 30 long as they exhibit the desired biological activity (U.S. Patent No. 4,816,567; and Morrison et al, Proc. Natl. Acad. Sci. USA, 81:6851-6855 (1984)). Chimeric antibodies of interest 4179172_1 (GHMatters) P89111.AU.1 -36 herein include "primatized" antibodies comprising variable domain antigen-binding sequences derived from a non-human primate (e.g. Old World Monkey, Ape etc) and human constant region sequences. "Humanized" forms of non-human (e.g., rodent) antibodies are chimeric antibodies that 5 contain minimal sequence derived from non-human immunoglobulin. For the most part, humanized antibodies are human immunoglobulins (recipient antibody) in which residues from a hypervariable region of the recipient are replaced by residues from a hypervariable region of a non-human species (donor antibody) such as mouse, rat, rabbit or nonhuman primate having the desired specificity, affinity, and capacity. In some instances, framework 10 region (FR) residues of the human immunoglobulin are replaced by corresponding non human residues. Furthermore, humanized antibodies may comprise residues that are not found in the recipient antibody or in the donor antibody. These modifications are made to further refine antibody performance. In general, the humanized antibody will comprise substantially all of at least one, and typically two, variable domains, in which all or 15 substantially all of the hypervariable loops correspond to those of a non-human immunoglobulin and all or substantially all of the FRs are those of a human immunoglobulin sequence. The humanized antibody optionally also will comprise at least a portion of an immunoglobulin constant region (Fc), typically that of a human immunoglobulin. For further details, see Jones et al., Nature 321:522-525 (1986); Riechmann et al., Nature 332:323-329 20 (1988); and Presta, Curr. Op. Struct. Biol. 2:593-596 (1992). Humanized HER2 antibodies include huMAb4D5-l, huMAb4D5-2, huMAb4D5-3, huMAb4D5-4, huMAb4D5-5, huMAb4D5-6, huMAb4D5-7 and huMAb4D5-8 or Trastuzumab (HERCEPTINTM) as described in Table 3 of U.S. Patent 5,821,337; humanized 520C9 (WO93/21319) and humanized 2C4 antibodies, such as Pertuzumab as described 25 further herein below. For the purposes herein, "Trastuzumab", "HERCEPTINTM" and "huMAb4D5-8" refer to an anti-HER2 antibody directed against the 4D5 epitope. Such antibody preferably comprises the light and heavy chain amino acid sequences disclosed e.g. in Fig. 14 of WO 2006/044908. 30 The "epitope 4D5" is the region in the extracellular domain of HER2 to which the antibody 4D5 (ATCC CRL 10463) and Trastuzumab bind. This epitope is close to the 41791721 (GHMatters) P89111 .AU.1 -37 transmembrane domain of HER2, and within Domain IV of HER2. To screen for antibodies which bind to the 4D5 epitope, a routine cross-blocking assay such as that described in Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory, Ed Harlow and David Lane (1988), can be performed. Alternatively, epitope mapping can be performed to assess 5 whether the antibody binds to the 4D5 epitope of HER2 (e.g. any one or more residues in the region from about residue 529 to about residue 625, inclusive, of HER2). The "epitope 7C2/7F3" is the region at the amino terminus, within Domain I, of the extracellular domain of HER2 to which the 7C2 and/or 7F3 antibodies bind. To screen for antibodies which bind to the 7C2/7F3 epitope, a routine cross-blocking assay such as that described in "Antibodies, A 10 Laboratory Manual" (Cold Spring Harbor Laboratory, Ed Harlow and David Lane (1988)) can be performed. Alternatively, epitope mapping can be performed to establish whether the antibody binds to the 7C2/7F3 epitope on HER2 (e.g. any one or more of residues in the region from about residue 22 to about residue 53 of HER2). Herein, "Pertuzumab" and "rhuMAb 2C4" refer to an antibody that binds to the 2C4 15 epitope and preferably comprising the variable light and variable heavy amino acid sequences disclosed in WO 2006/044908, more particularly the humanized 2C4 version 574 disclosed in Fig. 2 of WO 2006/044908. The "epitope 2C4" is the region in the extracellular domain of HER2 to which the antibody 2C4 binds. In order to screen for antibodies which bind to the 2C4 epitope, a routine 20 cross-blocking assay such as that described in Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory, Ed Harlow and David Lane (1988), can be performed. Alternatively, epitope mapping can be performed to assess whether the antibody binds to the 2C4 epitope of HER2. Epitope 2C4 comprises residues from domain II in the extracellular domain of HER2. 2C4 and Pertuzumab bind to the extracellular domain of HER2 at the junction of domains I, 25 II and III (Franklin et al. Cancer Cell 5:317-328 (2004)). A "growth inhibitory agent" when used herein refers to a compound or composition which inhibits growth of a cell, especially a HER expressing cancer cell either in vitro or in vivo. Thus, the growth inhibitory agent may be one which significantly reduces the percentage of HER expressing cells in S phase. Examples of growth inhibitory agents include 30 agents that block cell cycle progression (at a place other than S phase), such as agents that induce GI arrest and M-phase arrest. Classical M-phase blockers include the vincas (vincristine and vinblastine), taxanes, and topo II inhibitors such as doxorubicin, epirubicin, 41791721 (GHMatters) P8911 l.AU.1 -38 daunorubicin, etoposide, and bleomycin. Those agents that arrest G1 also spill over into S phase arrest, for example, DNA alkylating agents such as tamoxifen, prednisone, dacarbazine, mechlorethamine, cisplatin, methotrexate, 5-fluorouracil, and ara-C. Further information can be found in" The Molecular Basis of Cancer", Mendelsohn and Israel, eds., Chapter 1, 5 entitled "Cell cycle regulation, oncogenes, and antineoplastic drugs" by Murakami et al. (WB Saunders: Philadelphia, 1995), especially p. 13. Examples of "growth inhibitory" antibodies are those which bind to HER2 and inhibit the growth of cancer cells overexpressing HER2. Preferred growth inhibitory HER2 antibodies inhibit growth of SK-BR-3 breast tumor cells in cell culture by greater than 20%, 10 and preferably greater than 50% (e.g. from about 50% to about 100%) at an antibody concentration of about 0.5 to 30 .tg/ml, where the growth inhibition is determined six days after exposure of the SK-BR-3 cells to the antibody (see U.S. Patent No. 5,677,171 issued October 14, 1997). The preferred growth inhibitory antibody is a humanized variant of murine monoclonal antibody 4D5, e.g., Trastuzumab. 15 "Treatment" refers to both therapeutic treatment and prophylactic or preventative measures. Those in need of treatment include those already with the disease as well as those in which the disease is to be prevented. Hence, the patient to be treated herein may have been diagnosed as having the disease or may be predisposed or susceptible to the disease. The term "cytotoxic agent" as used herein refers to a substance that inhibits or prevents 20 the function of cells and/or causes destruction of cells. The term is intended to include radioactive isotopes (e.g. At m, I', JI25, y 9 o, Re 86 , Re 88 , Sm' 53 , Bim, p 2 and radioactive isotopes of Lu), chemotherapeutic agents, and toxins such as small molecule toxins or enzymatically active toxins of bacterial, fungal, plant or animal origin, including fragments and/or variants thereof 25 A "chemotherapeutic agent" is a chemical compound useful in the treatment of cancer. Examples of chemotherapeutic agents include alkylating agents such as thiotepa and cyclosphosphamide (CYTOXAN

TM

); alkyl sulfonates such as busulfan, improsulfan and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; ethylenimines and methylamelamines including altretamine, triethylenemelamine, 30 trietylenephosphoramide, triethiylenethiophosphoramide and trimethylolomelarnine; acetogenins (especially bullatacin and bullatacinone); delta-9-tetrahydrocannabinol 4179172.1 (GHMatters) P89111AU.1 -39 (dronabinol, MARENOL T M ); beta-lapachone; lapachol; colchicines; betulinic acid; a camptothecin (including the synthetic analogue topotecan (HYCAMTIN

TM

), CPT- 11 (irinotecan, C AMPTOSARTM), acetylcamptothecin, scopolectin, and 9-aminocamptothecin); bryostatin; callystatin; CC-1065 (including its adozelesin, carzelesin and bizelesin synthetic 5 analogues); podophyllotoxin; podophyllinic acid; teniposide; cryptopihycins (particularly cryptophycin I and cryptophycin 8); dolastatin; duocarmycin (including the synthetic analogues,KW-2189 and CBl-TMl); eleutherobin; pancratistatin; a sarcodictyin; spongistatin; nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, 10 novembichin, phenesterine, prednimustine, trofosfa[pi]nide, uracil mustard; nitrosureas such as carmustine, chlorozotocin, fotemustine, lomustine, nimustine, and ranirnnustine; antibiotics such as the enediyne antibiotics (e. g., calicheamicin, especially calicheamicin gamma 11 and calicheamicin omega 11 (see, e.g., Angew, Chemie Intl. Ed. Engl., 33: 183 186 (1994)); dynemicin, including dynemicin A; an esperamicin; as well as neocarzinostatin 15 chromophore and related chromoprotein enediyne antiobiotic chromophores), aclacinomysins, actinomycin, authramycin, azaserine, bleomycins, cactinornycin, carabicin, carminomycin, carzinophilin, chromomycinis, dactinomycin, daunorubicin, detorubicin, 6-diazo-5-oxo-L norleucine, doxorubicin (including ADRIAMYCINTM, morpholino-doxorubicin, cyanomorpholino-doxorubicin, 2-pyrrolino- doxorubicin, doxorubicin HC1 liposome 20 injection (DOXILTM), liposomal doxorubicin TLC D-99 (MYOCET

TM

), peglylated liposomal doxorubicin (CAELYXTM), and deoxydoxorubicin), epirubicin, esorubicin, idarubicin, marcellomycin, mitomycins such as mitomycin C, mycophenolic acid, nogalamycin, olivomycins, peplomycin, potfiromycin, puromycin, quelamycin, rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex, zinostatin, zorubicin; anti-metabolites such as 25 methotrexate, gemcitabine (GEMZARTM), tegafur (UFTORAL T M ), capecitabine (XELODATM), an epothilone, and 5-fluorouracil (5-FU); folic acid analogues such as denopterin, methotrexate, pteropterin, trimetrexate; purine analogs such as fludarabine, 6 mercaptopurine, thiamiprine, thioguanine; pyrimidine analogs such as ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxuridine; 30 anti-adrenals such as aminoglutethimide, mitotane, trilostane; folic acid replenisher such as frolinic acid; aceglatone; aldophosphamide glycoside; aminolevulinic acid; eniluracil; amsacrine; bestrabucil; bisantrene; edatraxate; defofamine; demecolcine; diaziquone; elfornithine; elliptinium acetate; etoglucid; gallium nitrate; hydroxyurea; lentinan; 4179172.1 (GHMatters) P891 11.AU.1 -40 lonidainine; maytansinoids such as maytansine and ansamitocins; mitoguazone; mitoxantrone; mopidanmol; nitraerine; pentostatin; phenamet; pirarubicin; losoxantrone; 2-ethylhydrazide; procarbazine; PSKLTM polysaccharide complex (JHS Natural Products, Eugene, OR); razoxane; rhizoxin; sizofiran; spirogermaraium; tenuazonic acid; triaziquone; 2,2',2" 5 trichlorotriethylamine; trichothecenes (especially T-2 toxin, verracurin A, roridin A and anguidine); urethan; dacarbazine; mannomustine; mitobronitol; mitolactol; pipobroman; gacytosine; arabinoside ("Ara-C"); thiotepa; taxoid, e.g., paclitaxel (TAXOLTM), albumin engineered nanoparticle formulation of paclitaxel (ABRAXANETM ), and docetaxel

(TAXOTERE

TM

); chloranbucil; 6-thioguanine; mercaptopurine; metliotrexate; platinum 10 agents such as cisplatin, oxaliplatin, and carboplatin; vincas, which prevent tubulin polymerization from forming microtubules, including vinblastine (VELBANTM), vincristine (ONCOVINTM), vindesine (ELDISINE TM ), FILDESINTM), and vinorelbine (NAVELBINETM)); etoposide (VP-16); ifosfamide; mitoxantrone; leucovovin; novantrone; edatrexate; daunomycin; aminopterin; ibandronate; topoisomerase inhibitor RFS 2000; 15 difluorometlhylornithine (DMFO); retinoids such as retinoic acid, including bexarotene

(TARGRETIN

TM

); bisphosphonates such as clodronate (for example, BONEFOSTM or OSTACTM), etidronate (DIDROCAL

TM

), NE- 58095, zoledronic acid/zoledronate

(ZOMETA

TM

), alendronate (FOSAMAJXTM), pamidronate (AREDIATM), tiludronate (SKELIDTM), or risedronate (ACTONEL

TM

); troxacitabine (a 1,3-dioxolane nucleoside 20 cytosine analog); antisense oligonucleotides, particularly those that inhibit expression of genes in signaling pathways implicated in aberrant cell proliferation, such as, for example, PKC-alpha, Raf, H-Ras, and epidermal growth factor receptor (EGF-R); vaccines such as THERATOPETM vaccine and gene therapy vaccines, for example, ALLOVECTINTM vaccine, LEUVECTINTM vaccine, and VAXIDTM vaccine; topoisomerase 1 inhibitor (e.g., 25 LURTOTECANTM); rmRH (e.g., ABARELIXTM); BAY439006 (sorafenib; Bayer); SU 11248 (Pfizer); perifosine, COX-2 inhibitor (e.g. celecoxib or etoricoxib), proteosome inhibitor (e.g. PS341); bortezomib (VELCADETM); CCI-779; tipifarnib (R1 1577); orafenib, ABT5 10; Bcl-2 inhibitor such as oblimersen sodium (GENASENSE

TM

); pixantrone; EGFR inhibitors (see definition below); tyrosine kinase inhibitors (see definition below); and 30 pharmaceutically acceptable salts, acids or derivatives of any of the above; as well as combinations of two or more of the above such as CHOP, an abbreviation for a combined therapy of cyclophosphamide, doxorubicin, vincristine, and prednisolone, and FOLFOX, an 4179172_1 (GHMatters) P89111.AU.1 -41 abbreviation for a treatment regimen with oxaliplatin (ELOXATIN

TM

) combined with 5-FU and leucovovin. Also included in this definition are anti-hormonal agents that act to regulate or inhibit hormone action on tumors such as anti-estrogens with mixed agonist/antagonist profile, 5 including, tamoxifen (NOLVADEXTM), 4-hydroxytamoxifen, toremifene (FARESTON

TM

), idoxifene, droloxifene, raloxifene (EVTSTATM), trioxifene, keoxifene, and selective estrogen receptor modulators (SERMs) such as SERM3; pure anti-estrogens without agonist properties, such as fulvestrant (FASLODEX T M ), and EM800 (such agents may block estrogen receptor (ER) dimerization, inhibit DNA binding, increase ER turnover, and/or suppress ER levels); 10 aromatase inhibitors, including steroidal aromatase inhibitors such as formestane and exemestane (AROMASIN

TM

), and nonsteroidal aromatase inhibitors such as anastrazole (ARIMIDEXTM), letrozole (FEMARATM) and aminoglutethimide, and other aromatase inhibitors including vorozole (RIVISOR T M ), megestrol acetate (MEGASETM), fadrozole, imidazole; lutenizing hormone-releasing hormone agonists, including leuprolide 15 (LUPRON T M and ELIGARDTM), goserelin, buserelin, and tripterelin; sex steroids, including progestines such as megestrol acetate and medroxyprogesterone acetate, estrogens such as diethylstilbestrol and premarin, and androgens/retinoids such as fluoxymesterone, all transretionic acid and fenretinide; onapristone; anti-progesterones; estrogen receptor down regulators (ERDs); anti-androgens such as flutamide, nilutamide and bicalutamide; 20 testolactone; and pharmaceutically acceptable salts, acids or derivatives of any of the above; as well as combinations of two or more of the above. As used herein, the term "EGFR-targeted drug" refers to a therapeutic agent that binds to EGFR and, optionally, inhibits EGFR activation. Examples of such agents include antibodies and small molecules that bind to EGFR. Examples of antibodies which bind to 25 EGFR include MAb 579 (ATCC CRL HB 8506), MAb 455 (ATCC CRL HB8507), MAb 225 (ATCC CRL 8508), MAb 528 (ATCC CRL 8509) (see, US Patent No. 4,943, 533, Mendelsohn et al.) and variants thereof, such as chimerized 225 (C225 or Cetuximab; ERBITUXTM) and reshaped human 225 (H225) (see, WO 96/40210, Imclone Systems Inc.); antibodies that bind type II mutant EGFR (US Patent No. 5,212,290); humanized and 30 chimeric antibodies that bind EGFR as described in US Patent No. 5,891,996; and human antibodies that bind EGFR, such as ABX-EGF (see W098/50433, Abgenix). The anti-EGFR antibody may be conjugated with a cytotoxic agent, thus generating an immunoconjugate 4179172_1 (GHMUers) P8911 1AU,1 -42 (see, e.g., EP-A-659439, Merck Patent GmbH). Examples of small molecules that bind to EGFR include ZD 1839 or Gefitinib (IRESSATM; Astra Zeneca), CP-358774 or Erlotinib HCI (TARCEVATM Genentech/Roche/OSI) and AG1478, AG1571 (SU 5271; Sugen) A "tyrosine kinase inhibitor" is a molecule which inhibits to some extent tyrosine 5 kinase activity of a tyrosine kinase such as a HER receptor. Examples of such inhibitors include the EGFR-targeted drugs noted in the preceding paragraph as well as small molecule HER2 tyrosine kinase inhibitor such as TAKI 65 available from Takeda, dual-HER inhibitors such as EKB-569 (available from Wyeth) which preferentially binds EGFR but inhibits both HER2 and EGFR-overexpressing cells, GW572016 (available from Glaxo) an oral HER2 and 10 EGFR tyrosine kinase inhibitor, and PKI- 166 (available from Novartis); pan-HER inhibitors such as canertinib (CI-1033; Pharmacia); Raf-1 inhibitors such as antisense agent ISIS-5132 available from ISIS Pharmaceuticals which inhibits Raf-1 signaling; non-HER targeted TK inhibitors such as Imatinib mesylate (GleevecTM) available from Novartis; MAPK extracellular regulated kinase I inhibitor CI-1040 (available from Pharmacia); quinazolines, 15 such as PD 153035,4-(3-chloroanilino) quinazoline; pyridopyrimidines; pyrimidopyrimidines; pyrrolopyrimidines, such as CGP 59326, CGP 60261 and CGP 62706; pyrazolopyrimidines, 4-(phenylamino-7H-pyrrolo[2,3-d] pyrimidines; curcumin (diferuloyl methane, 4,5-bis (4 fluoroanilino)phthalimide); tyrphostines containing nitrothiophene moieties; PD-0183805 (Warner-Larnber); antisense molecules (e.g. those that bind to HER-encoding nucleic acid); 20 quinoxalines (US Patent No. 5,804,396); tryphostins (US Patent No. 5,804,396); ZD6474 (Astra Zeneca); PTK-787 (Novartis/Schering AG); pan-HER inhibitors such as CI- 1033 (Pfizer); Affinitac (ISIS 3521; Isis/Lilly); PKI 166 (Novartis); GW2016 (Glaxo SmithKline); CI-1033 (Pfizer); EKB-569 (Wyeth); Semaxinib (Sugen); ZD6474 (AstraZeneca); PTK- 787 (Novartis/Schering AG); INC-IC l1 (Imelone); or as described in any of the following patent 25 publications: US Patent No. 5,804,396; W099/09016 (American Cyanamid); W098/43960 (American Cyanamid); W097/38983 (Warner Lambert); W099/06378 (Warner Lambert); W099/06396 (Warner Lambert); W096/30347 (Pfizer, Inc); W096/33978 (Zeneca); W096/3397 (Zeneca); and W096/33980 (Zeneca). An "anti-angiogenic agent" refers to a compound which blocks, or interferes with to 30 some degree, the development of blood vessels. The anti-angiogenic factor may, for instance, be a small molecule or antibody that binds to a growth factor or growth factor receptor involved in promoting angiogenesis. The preferred anti-angiogenic factor herein is an 41791721 (GHMatters) P89111.AU.1 -43 antibody that binds to Vascular Endothelial Growth Factor (VEGF), such as Bevacizumab (AVASTINTM). The term "cytokine" is a generic term for proteins released by one cell population which act on another cell as intercellular mediators. Examples of such cytokines are 5 lymphokines, monokines, and traditional polypeptide hormones. Included among the cytokines are growth hormone such as human growth hormone, N-methionyl human growth hormone, and bovine growth hormone, parathyroid hormone, thyroxine, insulin, proinsulin, relaxin; prorelaxin, glycoprotein hormones such as follicle stimulating hormone (FSH), thyroid stimulating hormone (TSH), and luteinizing hormone (LH), hepatic growth factor; 10 fibroblast growth factor, prolactin, placental lactogen, tumor necrosis factor a and P, mullerian-inhibiting substance, mouse gonadotropin-associated peptide, inhibin; activin, vascular endothelial growth factor, integrin, thrombopoietin (TPO), nerve growth factors such as NGF-P, platelet-growth factor; transforming growth factors (TGFs) such as TGF-a and TGF-, insulin-like growth factor-I and -II, erythropoietin (EPO), osteoinductive factors; 15 interferons such as interferon-a, -P, and -y, colony stimulating factors (CSFs) such as macrophage-CSF (M-CSF), granulocyte-macrophage-CSF (GM-CSF), and granulocyte-CSF (G-CSF), interleukins (ILs) such as IL-I, IL-la, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, a tumor necrosis factor such as TNF-a or TNF-3, and other polypeptide factors including LIF and kit ligand (KL). As used herein, the term cytokine includes proteins 20 from natural sources or from recombinant cell culture and biologically active equivalents of the native sequence cytokines. The term "effective amount" refers to an amount which provides the desired effect. In the case of a formulation ingredient such as the hyaluronidase enzyme in accordance with the present invention an effective amount is the amount necessary to increase the dispersion and 25 absorption of the co-administered anti-HER2 antibody in such a way that the anti-HER2 antibody can act in a therapeutically effective way as outline above. In the case of a pharmaceutical drug substance it is the amount of active ingredient effective to treat a disease in the patient. Where the disease is cancer, the effective amount of the drug may reduce the number of cancer cells; reduce the tumor size; inhibit (i.e., slow to some extent and 30 preferably stop) cancer cell infiltration into peripheral organs; inhibit (i.e., slow to some extent and preferably stop) tumor metastasis; inhibit, to some extent, tumor growth; and/or relieve to some extent one or more of the symptoms associated with the cancer. To the extent 41791721 (GHMOtOrs) P89111AU.1 -44 the drug may prevent growth and/or kill existing cancer cells, it may be cytostatic and/or cytotoxic. The effective amount may extend progression free survival, result in an objective response (including a partial response, PR, or complete response, CR), increase overall survival time, and/or improve one or more symptoms of cancer. 5 The antibody which is formulated in accordance with the present invention is preferably essentially pure and desirably essentially homogeneous (i.e. free from contaminating proteins etc, whereby the hyaluronidase enzyme in the formulation in accordance of this invention is not to be considered to be a contaminating protein of the anti HER2 monoclonal antibody in accordance of the present invention). An "essentially pure" 10 antibody means a composition comprising at least about 90% by weight of the antibody, based on total weight of the composition, preferably at least about 95% by weight. An "essentially homogeneous" antibody means a composition comprising at least about 99% by weight of antibody, based on total weight of the composition. The invention will be more fully understood by reference to the following Examples. 15 They should not, however, be construed as limiting the scope of the invention. All literature and patent citations are incorporated herein by reference. The Examples are further illustrated by the appended figures, which show the following experimental results: Fig. 1 Stability of the formulations A to F (see Table 1 below) after 8 weeks with 20 respect to Low Molecular Weight (LMW) Species detected by Size Exclusion-HPLC. As shown in this figure the PS20 formulations A, C and E showed a slightly better stability than the PS80 formulations B, D and F upon storage at 300 C. Fig. 2 Stability of the formulations A to F (see Table I below) after 8 weeks with respect to High Molecular Weight (HMW) Species detected by Size Exclusion-HPLC. As 25 shown in this figure the formulations A and B that contain trehalose without the addition of sodium chloride show a smaller increase of HMWs after 8 weeks storage time. Fig. 3 Stability after 8 weeks with respect to turbidity. As shown in this figure trehalose containing formulations A and B show a low turbidity; whereas NaCl containing formulations C to F show a much higher turbidity. Formulations E and F containing trehalose 4179172_1 (GHMatters) P89111AU.1 -45 as well as NaCl showed an intermediate turbidity. No significant increase was observed upon storage for 8 weeks. Fig. 4 Viscosity of liquid formulations A to F (see Table 1 below) as measured by using plate-cone viscosimetry at ambient temperature. All formulations are in a low viscosity 5 range that allows for subcutaneous injection. Examples The anti-HER2 formulations for subcutaneous administration according to the invention were developed based on the experimental results as provided below using the 10 general preparatory and analytical methods and assays as outlined below. A) Preparation of the components for the formulation Trastuzumab is manufactured by techniques generally known for the production of recombinant proteins. A genetically engineered Chinese hamster ovary cell (CHO) line prepared as described in EP-B-590058 is expanded in cell culture from a master cell bank. 15 The Trastuzumab monoclonal antibody is harvested from the cell culture fluid and purified using immobilized Protein A affinity chromatography, cation exchange chromatography (e.g. SP-Sepharose FF), a filtration step to remove viral contaminations (e.g. a PVDF membrane (sold by Milipore under the name Viresolve filters), followed by anion exchange chromatography (e.g. Q-Sepharose FF) and an ultrafiltration/diafiltration step. For preparing 20 the formulations in accordance with these examples the Trastuzumab was provided at a concentration of approx. 100 mg/ml in a 20 mM histidine buffer at a pH of approximately 6.0. rHuPH20 is manufactured by techniques generally known from the production of recombinant proteins. The process begins with thawing of cells from the working cell bank (WCB) or master cell bank (MCB) and expansion through cell culture in a series of spinner 25 flasks followed by expansion in a bioreactor. After completion of the production phase, the cell culture liquid is clarified by filtration, and is then treated with solvent/detergent to inactivate viruses. The protein is then purified by a series of column chromatography processes to remove process and product related impurities. A viral filtration step is performed, and the filtered bulk is then concentrated, formulated into the final buffer: 10 4179172.1 (GHMOIters) P0911l.AU.1 -46 mg/mL rHuPH20 in 20 mM L-histidine/HCl buffer, pH 6.5, 130 mM NaCl, 0.05% (w/v) polysorbate 80. The rHuPH20 bulk is stored below -70'C. The other excipients of the formulation in accordance with the present invention are widely used in the practice and known to the person skilled in the art. There is therefore no 5 need to be explained them here in detail. Liquid drug product formulations for subcutaneous administration according to the invention were developed as follows. Example 1: Preparation of the liquid formulations 10 For the preparation of the liquid formulations Trastuzumab was buffer-exchanged against a diafiltration buffer containing the anticipated buffer composition and, when required, concentrated by diafiltration to an antibody concentration of approx. 150 mg/ml. After completion of the diafiltration operation, the excipients (e.g. trehalose, rHuPH20) were added 15 as stock solutions to the antibody solution. The surfactant was then added as a 50 to 200-fold stock solution. Finally the protein concentration was adjusted with a buffer to the final Trastuzumab concentration of about 110 mg/ml, 120 mg/ml or 130 mg/ml as specified in the particular formulations further below. 20 All formulations were sterile-filtered through 0.22 pm low protein binding filters and aseptically filled into sterile 6 ml glass vials closed with ETFE (Copolymer of ethylene and tetrafluoroethylene)-coated rubber stoppers and alucrimp caps. The fill volume was approx. 3.0 ml. These formulations were stored at different climate conditions (5 0 C, 25*C and 30*C) for different intervals of time and stressed by shaking (1 week at a shaking frequency of 200 25 min-' at 5 0 C and 25*C) and freeze-thaw stress methods. The samples were analyzed before and after applying the stress tests by the following analytical methods: 1) UV spectrophotometry; 2) Size Exclusion Chromatography (SEC); 3) by Ion exchange chromatography (IEC); 30 4) by turbidity of the solution; 5) for visible particles; and 6) for rHuPH20 activity. 4179172_1 (GHMalters) P8911 1AU.1 -47 UV spectroscopy, used for determination of protein content, was performed on a Perkin Elmer 235 UV spectrophotometer in a wavelength range from 240 nm to 400 nm. Neat protein samples were diluted to approx. 0.5 mg/ml with the corresponding formulation buffer. 5 The protein concentration was calculated according to Equation 1. Equation 1: Protein content = A(280) - A(320) x dil.factor eKcm2 x d(cm) The UV light absorption at 280 rm was corrected for light scattering at 320 nm and multiplied with the dilution factor, which was determined from the weighed masses and densities of the neat sample and the dilution buffer. The numerator was divided by the 10 product of the cuvette's path length d and the extinction coefficient S. Size Exclusion Chromatography (SEC) was used to detect soluble high molecular weight species (aggregates) and low molecular weight hydrolysis products (LMW) in the formula tions. The method was performed on a Waters Alliance 2695 HPLC instrument with a Waters 15 W2487 Dual Absorbance Detector and equipped with 2 TosoHaas TSK Gel SuperSW3000, 4,6x300 mm columns in row. Intact monomer, aggregates and hydrolysis products were separated by an isocratic elution profile, using 50 mM sodium phosphate, 420 mM sodium perchlorate, pH 7. 0 as mobile phase, and were detected at a wavelength of 280 nm. 20 Ion Exchange Chromatography (IEC) was performed to detect chemical degradation products altering the net charge of Trastuzumab in the formulations. For this purpose Trastuzumab was digested with Carboxpeptidase B. The method used a suitable HPLC instrument equipped with a UV detector (detection wavelength 214 nm) and a Dionex ProPacTM WCX 10 Analytical cation-exchange column (4 x 250 mm). 10mM sodium phosphate buffer pH 7.5 25 in H 2 0 and 10 mM sodium phosphate buffer pH 7.5 and 100 mM NaCl were used as mobile phases A and B, respectively, with a flow rate of 0.8 ml/min. For the determination of the turbidity, opalescence was measured in FTU (turbidity units) using a HACH 2100AN turbidimeter at room temperature. Samples were analyzed for visible particles by using a Seidenader V90-T visual inspection 30 instrument. 4170172_1 (GHMatters) P8911l.AU.1 -48 An in vitro enzyme assay of rHuPH20 as hyaluronidase was used as activity assay. The assay is based on the formation of an insoluble precipitate when hyaluronan (sodium hyaluronate) binds to a cationic precipitant. Enzyme activity was measured by incubating rHuPH20 with hyaluronan substrate and then precipitating the undigested hyaluronan with acidified serum 5 albumin (horse serum). The turbidity was measured at a wavelength of 640 nim and the decrease in turbidity resulting from enzyme activity on the hyaluronan substrate is a measure of the enzyme activity. The procedure is run using a standard curve generated with dilutions of rHuPH20 assay reference standard, and sample activity is read from the curve. Further experiments were performed including following variations: 10 - variations in pH from about approx. 5.0 to approx. 6.0 - variations in protein content from about approx. 110 mg/ml to approx. 130 mg/ml - variations in surfactant from approx. 0.02% to approx. 0.06% - variations in stabilizer (methionine) from about 5 mM to about 15 mM 15 The compositions and the results of the stability testing for the liquid anti-HER-2 drug product formulations (Formulations A to X) are provided in Table 1 below wherein the following abbreviations are used: ffp:= free from particles; effp: = essentially free from particles; wafp: = with a few particles F/T: = freezing/thawing; skg: = shaking; nd: = not determined 20 The formulations specified below show that it is possible to provide liquid formulations with high concentrations of two different proteins. Such formulations can be prepared with greater ease and lower costs than lyophilized formulations. Moreover such formulations are easier to handle as no dissolving of the lyophilized final product (reconstitution) is required (ready to use). It has been found that the formulations specified in Tables 1, 3 and 4 are also suitable 25 for the formulation of highly concentrated, stable pharmaceutical formulation of pharmaceutically active anti-HER2 antibodies lacking the hyaluronidase enzyme. Therefore, in one aspect the present invention relates also to formulations having the specified ingredients but lacking the hyaluronidase enzyme. 41791721 (GHMOIttes) P09111AU.1 o o m tr m 0 0 m o o 00 I ca , V f ) zf - r ' T C -- - CD Cel 0 o - ON M N s to .-- e in on 0 t o0 e ~ o0 m0 t N in t N N N Nm a) 0, P. 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- - x o a 6b- rO ON o- t w - : o q 0-uC 00 - N - - N- 0 --- 00 r- - - - -C nCl Cl 0- Cl - C Cl enU O O 422 u T> 0~c 0 0 c ) N O N- O N- N- N- _ _ 0 ' '0 ' 0 . N4 Cl l c~8 0- N l- 0 N: Nl C' 0 ca cq Na2eiee o ~ ~ ~ c N q tf 0 LN N mO e t t o 0fll c q Cl CO In en e Io c N C N0 (C00 w N rn te Qo G oSo - 'n e no e rC C 0 r. bO C\ -\ (7 Cl 0 C D o0 0- - - r- - 0 N Nt 'C Cl -0 -0 ) 0- - "a - - r, r -go E e E - 'C 'C C n Lf 0n 0 en en Ct) -0 0 Cl H - - -- - - -- V 0 u 00 o So C. ON C C'O C ON ONON C 30 d.o 00) Nkx 4) -n -73 Example 2: Preparation of a lyophilized formulation A solution of approx. 60 mg/ml Trastuzumab was prepared as described above for liquid formulations. All excipients have been added at half of the concentration of the above 5 mentioned liquid formulation. The formulation was sterile filtered through 0.22 m filters and aseptically distributed in equal amounts into sterile 20 ml glass vials. The vials were partly closed with ETFE (Copolymer of ethylene and tetrafluoroethylene)-coated rubber stoppers suitable for the use in lyophilization processes and lyophilized using the freeze drying cycle reported in Table 2. 10 Table 2 Freeze-drying Cycle Shelf temperature Ramp Rate Hold time Vacuum Set point (*C)

(

0 C/min) (min) (pbar) Pre-cooling 5 0 C 0.0 60 Freezing -40 0 C 1.0 120 Primary Drying -25 0 C 0.5 4560 80 Secondary Drying +25 0 C 0.2 300 80 The product was first cooled from room temperature to approx 5 0 C (pre-cooling), followed by a freezing step at -40 0 C with a plate cooling rate of approx. 1 0 C/min, followed by a 15 holding step at -40*C for about 2 hours . The first drying step was performed at a plate temperature of approx. -25*C and a chamber pressure of approx. 80 pIbar for about 76 hours. Subsequently, the second drying step started with a temperature ramp of 0.2*C / min from 254C to 25*C, followed by a holding step at 25*C for at least 5 hours at a chamber pressure of approx. 80 tbar. 20 Lyophilization was carried out in a Usifroid SMH-90 LN2 freeze-dryer (Usifroid, Maurepas, France) or a LyoStar II Freeze-dryer (FTS Systems, Stone Ridge, NY, USA). The freeze dried samples were stored at different climate conditions (5 0 C, 25*C and 30'C) for different intervals of time. The lyophilized vials were reconstituted to a final volume of 2.65 ml with 25 water for injection (WFI) yielding an isotonic formulation with an antibody concentration of approx. 120 mg/ml. The reconstitution time of the freeze-dried cakes was around 10 min. 41791721 (HMatters) P89111.AU1 -74 Analysis of the reconstituted samples was performed after a 24 hour incubation period of the reconstituted liquid sample at ambient temperature. The samples were again analyzed by the following analytical methods described above: 1) UV spectrophotometry; 5 2) Size Exclusion Chromatography (SEC); 3) Ion exchange chromatography (IEC); 4) turbidity of the solution; and 5) for visible particles. The results of the stability testing for the Formulation Y is provided in the Table 3 below 10 wherein the following abbreviations are used: ffp: = free from particles; effp: = essentially free from particles; nd: = not determined 41791721 (GHMatters) PS911I.AU.1 o - o N N ' m in 00 E-~'0 ON N NC S .2: m oN N - o '0 C - - - - - S o e I Cl t. CC o= ) o e Q e 4 - o -os o o, -o - N a 0 . 0. 0 E w 6 6r 0 ', o C: o o Q 0 0 a o) ,N W, O, ON - 00 00 s o ONl oNN ON 6 6e - a6m 10o e oo Oo m - - 0 N . in oC 4 S2-l6 6 6 6 - -1 ~ n Cl) ON m -m mCN o N - - 8 CA CO C C 0 CA . 2 C 2 4 S0 .9t ~ ) ~ 2 ) C -~ 0. . . ffl CA 00 .. u o o eCt -76 The properties of the above formulations provided are summarized in the following Table 4: F Tr His tre NaCI Meth PS rHu 20 80 mg/mi m pH mM mM mM % % U/ml A 120 20 5.5 210 10 0.04 12'000 B 120 20 5.5 210 10 0.06 12'000 C 120 20 5.5 130 10 0.04 12'000 D 120 20 5.5 130 10 0.06 12'000 E 120 20 5.5 105 65 10 0.04 12'000 F 120 20 5.5 105 65 10 0.06 12'000 G 120 20 5.5 210 10 0.04 H 110 20 5.0 210 5 0.02 2'000 I 110 20 6.0 210 5 0.02 2'000 J 110 20 5.0 210 5 0.06 2'000 K 110 20 6.0 210 5 0.06 2'000 L 110 20 5.0 210 15 0.02 2'000 M 110 20 6.0 210 15 0.02 2'000 N 110 20 5.0 210 15 0.06 2'000 0 110 20 6.0 210 15 0.06 2'000 P 130 20 5.0 210 5 0.02 2'000 Q 130 20 6.0 210 5 0.02 2'000 R 130 20 5.0 210 5 0.06 2'000 S 130 20 6.0 210 5 0.06 2'000 T 130 20 5.0 210 15 0.02 2'000 U 130 20 6.0 210 15 0.02 2'000 V 130 20 5.0 210 15 0.06 2'000 W 130 20 6.0 210 15 0.06 2'000 X 120 20 5.5 210 10 0.04 2'000 Y 120 20 5.5 210 10 0.04 12'000 *) F = Formulation Tr = Trastuzumab His = L-histidine/HCl tre = a,a-trehalose dihydrate NaCl= Sodium Chloride met = methionine 5 PS = polysorbate in % (w/v) rHu = rHuPH20 = after reconstitution 4179172_1 (GHMaIers) P8911 1AU.1

Claims (33)

1. A highly concentrated, stable pharmaceutical liquid formulation of a pharmaceutically active anti-HER2 antibody for subcutaneous injection comprising: a. about 120 + 18 mg/ml Trastuzumab; 5 b. about I to 50 mM of histidine/HCl providing a pH of 5.5 + 0.6; c. about 15 to 250 mM of a,a-trehalose dihydrate or sucrose and about 5 to 25 mM of methionine; and d. about 0.01 to 0.08 % of a nonionic surfactant, wherein the highly concentrated, stable pharmaceutical liquid formulation lacks a 10 hyaluronidase enzyme.

2. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to claim 1 comprising about 110 mg/ml, about 120 mg/ml, or about 130 mg/ml of Trastuzumab. 15

3. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to claim 1 or claim 2 comprising 120 + 10 mg/ml of Trastuzumab.

4. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation 20 according to any one of claims 1 to 3 comprising about 120 mg/ml of Trastuzumab.

5. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to any one of claims 1 to 4, wherein the histidine buffer is 20 mM histidine/HCl. 25

6. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to any one of claims 1 to 5, wherein the a,a-trehalose dihydrate or sucrose concentration is about 210 mM. 30

7. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to any one of claims 1 to 6, wherein the nonionic surfactant is a polysorbate selected from the group consisting of polysorbate 20, polysorbate 80 and polyethylene-polypropylene copolymer. 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 78

8. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to claim 7, wherein the concentration of the polysorbate is 0.02 % (w/v), 0.04 % (w/v) or 0.06 % (w/v). 5

9. A highly concentrated, stable pharmaceutical liquid formulation of a pharmaceutically active anti-HER2 antibody for subcutaneous injection essentially consisting of 120 mg/ml Trastuzumab, 20 mM L-histidine/HCl pH 5.5, 210 mM a,a-trehalose dihydrate, 10 mM methionine and 0.04% polysorbate 20. 10

10. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to any one of claims 1 to 9 that is stable upon freezing and thawing.

11. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation 15 according to any one of claims I to 10 that is ready to use.

12. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to any one of claims I to 11 for combination with 150 to about 16'000 U/ml, 2'000 U/ml, or 12'000 U/ml of a hyaluronidase enzyme. 20

13. A pharmaceutical formulation comprising a highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to any one of claims I to 12 combined with 150 to about 16'000 U/ml, 2'000 U/ml, or 12'000 U/ml of a hyaluronidase enzyme. 25

14. Use of: a. about 120 + 18 mg/ml Trastuzumab; b. about I to 50 mM of histidine/HCl providing a pH of 5.5 + 0.6; c. about 15 to 250 mM of a,a-trehalose dihydrate or sucrose and about 5 to 30 25 mM of methionine; and d. about 0.01 to 0.08 % of a nonionic surfactant, 5859357_1 (GHMatters) P89111.AU.1 LEOWNR

15-Oct-14 79 in the manufacture of a medicament for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non malignant disease, wherein the medicament lacks a hyaluronidase enzyme. 5 15. Use of a formulation according to any one of claims I to 13 in the manufacture of a medicament for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease.

16. Use of a formulation according to any one of claims I to 12 in combination with a 10 hyaluronidase enzyme in the manufacture of a medicament for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease.

17. Use of a formulation according to any one of claims I to 12 in combination with 15 10 mg/ml rHuPH20 in 20 mM His/Histidine HCl, pH 6.5, 130 mM NaCl, 0.05% (w/v) polysorbate 80 in the manufacture of a medicament for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease. 20

18. A method for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease, comprising administering to the subject a formulation according to any one of claims I to 13 in an amount effective to treat the disease or disorder. 25

19. A method for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease, comprising administering to the subject a formulation according to any one of claims I to 12 in combination with a hyaluronidase enzyme. 30

20. A method for treating in a subject a disease or disorder amenable to treatment with an anti-HER2 antibody, optionally cancer or a non-malignant disease, comprising administering to the subject a formulation according to any one of claims I to 12 in 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 80 combination with 10 mg/ml rHuPH20 in 20 mM His/Histidine HCl, pH 6.5, 130 mM NaCl, 0.05% (w/v) polysorbate 80.

21. Use or a method according to any one of claims 14 to 20 wherein the cancer is gastric 5 cancer, metastatic breast cancer or early breast cancer.

22. Use or a method according to any one of claims 14 to 21 wherein treating comprises coadministering the medicament or formulation concomitantly or sequentially with a chemotherapeutic agent. 10

23. Use or a method according to any one of claims 14 to 22 wherein treating comprises administering the medicament or formulation to the subject subcutaneously.

24. An injection device comprising a formulation according to any one of claims I to 12. 15

25. The injection device according to claim 24 wherein the device provides for coadministration of 150 to about 16'000 U/ml, 2'000 U/ml, or 12'000 U/ml of a hyaluronidase enzyme. 20

26. An injection device comprising a formulation according to claim 13.

27. A kit comprising one or more vials containing a formulation according to any one of claims 1 to 12, optionally when used according to a method according to any one of claims 18 to 23. 25

28. A kit according to claim 27 further comprising one or more vials containing a hyaluronidase enzyme, wherein the kit provides for coadministration of 150 to about 16'000 U/ml, 2'000 U/ml, or 12'000 U/ml of the hyaluronidase enzyme. 30

29. A kit comprising one or more vials containing a formulation according to claim 13, optionally when used according to a method according to any one of claims 18 or 21 to 23. 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14 81

30. A kit according to any one of claims 27 to 29 further comprising an injection device that administers the formulation to a subject, optionally subcutaneously.

31. A kit comprising the injection device according to any one of claims 24 to 26. 5

32. A formulation according to claim 12 or claim 13, use according to claim 16, a method according to claim 19, an injection device according to claim 25, or a kit according to claim 28, wherein the hyaluronidase enzyme is rHuPH20. 10

33. A highly concentrated, stable pharmaceutical anti-HER2 antibody liquid formulation according to claim 1 or claim 9, a pharmaceutical formulation according to claim 13, use according to any one of claims 14 to 17, a method according to any one of claims 18 to 20, an injection device according to claim 24 or claim 26, or a kit according to any one of claims 27, 29 or 31, substantially as hereinbefore described 15 with reference to the examples and figures. 5859357_1 (GHMatters) P89111.AU.1 LEOWNR 15-Oct-14