WO2017147274A1 - An improved formulation of long-acting levonorgestrel butanoate injectable depot suspension - Google Patents
An improved formulation of long-acting levonorgestrel butanoate injectable depot suspension Download PDFInfo
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- WO2017147274A1 WO2017147274A1 PCT/US2017/019092 US2017019092W WO2017147274A1 WO 2017147274 A1 WO2017147274 A1 WO 2017147274A1 US 2017019092 W US2017019092 W US 2017019092W WO 2017147274 A1 WO2017147274 A1 WO 2017147274A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
- A61K31/567—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in position 17 alpha, e.g. mestranol, norethandrolone
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/02—Inorganic compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/38—Cellulose; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
- A61K9/0024—Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/18—Feminine contraceptives
Definitions
- the present invention relates to an improved formulation of a long-acting injectable depot suspension of Levonorgestrel Butanoate (LB) for contraceptive use and treatment or prevention of reproductive tract disorders.
- LB Levonorgestrel Butanoate
- Contraceptive compositions based on esters of Levonorgestrel (LNG) have been disclosed in European Patent EP0129947B1.
- LNG is a safe and effective progestin contraceptive agent however its duration of action is relatively short when dosed orally and must be taken daily.
- LB is an esterified version of LNG with longer acting contraceptive properties especially when injected as an aqueous suspension depot formulation (Long- Acting Contraceptive Agents: Design of the WHO Chemical Synthesis Programme. Steroids. 1983 Mar; 41(3):243-53).
- Progestin-only contraceptives are advantageous since they have a long-track record of safety and effectiveness and avoid estrogen-related side effects (Benefits and Risks of Oral Contraceptives. Am J Obstet Gynecol. 1999 Jun; 180(6 Pt 2): S343-8). Furthermore, long-acting progestin-only injectable contraceptives are desirable since they do not require daily dosing like oral contraceptives and are very effective when given at the required intervals. There are currently two injectable progestins, medroxyprogesterone acetate and norethindrone enanthate (also known as norethisterone enanthate), in use as long-acting contraceptive agents.
- medroxyprogesterone acetate and norethindrone enanthate also known as norethisterone enanthate
- DMPA Depot medroxyprogesterone acetate
- NET -EN Norethindrone enanthate
- LB injectable is particularly advantageous since LB is more potent than the two existing agents (DMPA and NET -EN) exerting its contraceptive activity for a longer period while allowing for a decreased steroid load.
- LB has been shown to suppress ovulation in women for 5-6 months when injected at a single dose of 50 mg formulated as a micronized aqueous suspension (Garza-Flores J, Hall PE, Perez-Palacios G. Long- Acting Hormonal Contraceptives for Women. J Steroid Biochem Molec Biol 1991;40: 697-704).
- injectable LB were found to aggregate over time, resulting in loss of product stability and reproducibility of the clinical batches.
- a new stable formulation of LB has been developed and clinical testing at a dose of 20 mg (in 1 mL) showed a 3 -month suppression of ovulation (Levonorgestrel Butanoate Intramuscular Injection Does Not Reliably Suppress Ovulation for 90 Days in Obese and Normal BMI Women: A Pilot Study, http://dx.doi.Org/10.1016/i .contraception.2016.07.018). While the duration of action of new LB formulation is similar to that of DMPA and NET -EN, it falls short of the previously demonstrated 5-6 months and the preferred target product profile. Additional optimization of the formulation was conducted, and tested in non-human primates. With an improved and stable particle size formulation, duration of action up to 6 months was observed in non-human primates.
- the decreased steroid load of LB may reduce the potential for undesirable side effects such as amenorrhea and hypoestrogenism which is frequently seen with DMPA.
- DMPA is also increasingly being associated with higher risk for sexual HIV acquisition, possibly related to its significant hypoestrogenism (DMPA Use and HIV Acquisition: Time to Switch to NET-EN? The Lancet HIV,
- long-acting progestins such as LB
- LB long-acting progestins
- the present application discloses modified formulation compositions and manufacturing processes that address the limitations of earlier compositions.
- the present invention provides an extended duration injectable depot composition of Levonorgestrel Butanoate (LB) where the composition is a sterile aqueous depot suspension comprising non-aggregated LB particles with a median (Dso) particle size in the range of 5 - 50 ⁇ , more particularly in the range of 10-30 ⁇ and in other cases in the range of 13 - 35 ⁇ , 13 - 40 ⁇ , 13 - 50 ⁇ , 15 - 35 ⁇ , 15 - 40 ⁇ , 15 - 50 ⁇ , 20 - 35 ⁇ , 20 - 40 ⁇ , or 20 - 50 ⁇ .
- LB Levonorgestrel Butanoate
- the depot composition additionally comprises at least one ingredient selected from the group consisting of: surfactant(s), solubilizer(s), emulsifier(s), preservative(s), isotonicity agent(s), dispersing agent(s), wetting agent(s), filler(s), solvent(s), buffering agent(s), stabilize ⁇ s), lubricant(s), thickening agent(s), flocculating agent(s), suspending agent(s), electrolytes, antioxidants, and chelating agent(s).
- surfactant(s) solubilizer(s), emulsifier(s), preservative(s), isotonicity agent(s), dispersing agent(s), wetting agent(s), filler(s), solvent(s), buffering agent(s), stabilize ⁇ s), lubricant(s), thickening agent(s), flocculating agent(s), suspending agent(s), electrolytes, antioxidants, and chelating agent(s).
- the depot composition comprises at least one of a wetting agent, a dispersing agent, a thickening agent, a buffering agent, and a preservative.
- the concentration of LB in the composition is 1 - 50 mg/mL and more particularly 10 - 20 mg/ml.
- a method of treating, ameliorating or preventing a progestin/progesterone-sensitive reproductive tract dysfunction or disorder comprises administering to a patient in need thereof a therapeutically effective amount of the depot composition disclosed herein.
- the dysfunction or disorder is selected from the group consisting of dysfunctional uterine bleeding, endometrial hyperplasia and cancer, endometriosis, fibroids, and PMS.
- contraception comprises administering to a patient in need thereof a therapeutically effective amount of the depot composition disclosed herein.
- the depot provides an extended duration of progestational action of at least 4 months.
- the progestational action effects contraceptive activity for an extended duration of at least 4 months.
- the depot composition comprises a wetting agent and/or dispersing agent selected from the group consisting of polyethoxylated sorbitan fatty acid esters, sorbitan fatty acid esters, polyoxyalkylene derivatives of propylene glycol, phosphatides, lecithin, polyoxyethylated fats, polyoxyethylated oleotriglycerides, linolizated oleotriglycerides, polyethylene oxide condensation products of fatty alcohols, and
- the depot composition comprises polysorbate 80.
- the depot composition comprises a wetting agent.
- the wetting agent is present in the composition at a concentration in the range of 0.05 - 2% w/v and more particularly 0.2% w/v.
- the dispersing agent comprises sorbitan monopalmitate.
- the depot composition comprises a dispersing agent. In some cases, the dispersing agent is present in the composition at a concentration in the range of 0.05 - 2% w/v and preferably 0.2% w/v.
- the depot composition comprises at least one thickening agent.
- the thickening agent is selected from the group consisting of sodium carboxymethyl cellulose, methyl cellulose, hydroxypropyl cellulose, calcium carboxymethyl cellulose, crosslinked carboxymethyl cellulose, hydroxyethylcellulose, hydroxypropylmethyl cellulose, polyvinyl alcohol, acacia, gelatin, and polyvinyl pyrrolidone.
- the depot composition comprises a thickening agent, which is present in the composition at a concentration in the range of 0.1 - 5% w/v and preferably 0.5 - 1.0% w/v.
- the thickening agent comprises sodium
- the depot composition comprises at least one preservative.
- the preservative is selected from the group consisting of benzyl alcohol, parabens, methyl paraben, propyl paraben, butyl paraben, benzalkonium chloride, thiomerosal, phenol, meta-cresol, chlorobutanol, phenylmercuric salts, phenylmercuric acetate, phenylmercuric borate, and phenylmercuric nitrate.
- the preservative comprises benzyl alcohol.
- the depot composition comprises a preservative, which is present in the composition at a concentration in the range of 0.1 - 5% v/v and preferably
- the depot composition comprises at least one buffer.
- the buffer is selected from the group consisting of acetate, citrate, tartrate, phosphate, and triethanolamine (TRIS).
- the buffer comprises phosphate
- a method of producing a sterile injectable depot composition of Levonorgestrel Butanoate comprises subjecting Levonorgestrel Butanoate to a size reduction and sterilization process to yield sterile micronized Levonorgestrel Butanoate with a median (Dso) particle size in the range of 5 - 50 ⁇ , more particularly in the range of 10-30 ⁇ and in other cases in the range of 13 - 35 ⁇ , 13 - 40 ⁇ , 13 - 50 ⁇ , 15 - 35 ⁇ , 15 - 40 ⁇ , 15 - 50 ⁇ , 20 - 35 ⁇ , 20 - 40 ⁇ , or 20 - 50 ⁇ and combining the sterile micronized Levonorgestrel Butanoate with a sterile aqueous vehicle to form the sterile injectable depot composition.
- Dso median
- the sterile micronized Levonorgestrel Butanoate is produced by sterile filtration and recrystallization followed by aseptic micronization.
- the sterile micronized Levonorgestrel Butanoate is produced by non-sterile dry or wet milling followed by gamma or e-beam irradiation sterilization.
- the sterile micronized Levonorgestrel Butanoate is produced by non-sterile spray drying followed by gamma or e-beam irradiation sterilization.
- the method includes preparing a first sterile aqueous solution comprising at least one pharmaceutically acceptable ingredient selected from the group consisting of a thickening agent, a buffering agent, and a preservative; preparing a second sterile aqueous solution comprising at least one pharmaceutically acceptable ingredient selected from the group consisting of a wetting agent and a dispersing agent; dispersing the sterile micronized Levonorgestrel Butanoate in the second sterile aqueous solution; and combining the second sterile aqueous solution containing the sterile micronized Levonorgestrel Butanoate with the first sterile aqueous solution to form the final sterile injectable depot composition.
- the first sterile aqueous solution comprises a thickening agent, buffering agent, and preservative.
- preparing the first sterile aqueous solution comprises adding the preservative to water for injection at a temperature of ⁇ 10°C; and dissolving the thickening agent in the water for injection containing the preservative. Following dissolution of the thickening agent, the buffering agent is added and dissolved.
- the second sterile aqueous solution comprises a wetting agent and dispersing agent.
- preparing the second sterile aqueous solution comprises adding the wetting agent and dispersing agent to water for injection; and homogenizing the mixture of wetting agent, dispersing agent, and water for injection to uniformly disperse the dispersing agent.
- combining the second sterile aqueous solution containing the sterile micronized Levonorgestrel Butanoate with the first sterile aqueous solution comprises adding the first sterile aqueous solution to the second sterile aqueous solution containing the sterile micronized Levonorgestrel Butanoate; and homogenizing the combined solutions to form a uniformly dispersed Levonorgestrel Butanoate suspension.
- FIG. 1 shows the results of a settling time study demonstrating that a sodium carboxymethyl cellulose concentration of 0.5 - 1.0% in the formulation is particularly useful for minimizing the effects of settling of the LB particles in the improved LB injectable depot suspension formulation.
- FIG. 2 shows the in vitro release data for the improved LB injectable depot suspension formulation micronized to different particle size ranges, demonstrating longer release of larger particle size LB formulations.
- FIG. 3 shows the particle size distribution obtained from dry milled levonorgestrel butanoate drug substance.
- FIG. 4 is a photomicrograph showing the particle size distribution obtained from dry milled levonorgestrel butanoate drug substance.
- FIG. 5 shows the particle size distribution obtained from rotor-stator wet milled (10% w/w suspension of LB in aqueous 0.05% Tween 80) levonorgestrel butanoate drug substance.
- FIG. 6 is a photomicrograph showing the particle size distribution obtained from rotor-stator wet milled (10% w/w suspension of LB in aqueous 0.05% Tween 80)
- FIG 7 shows the particle size distribution obtained from spray dried (5% w/w solution of LB in dichloromethane) levonorgestrel butanoate drug substance.
- FIG 8 is a photomicrograph showing the particle size distribution obtained from spray dried (5% w/w solution of LB in dichloromethane) levonorgestrel butanoate drug substance.
- the present invention provides an improved formulation and process for preparation of a long-acting injectable depot suspension formulation of LB.
- micronized LB within certain particle ranges and at least one dispersing and/or wetting agent (e.g., 0.2% w/v each of Tween ® 80 (polysorbate 80) and Span ® 40 (sorbitan monopalmitate)) corrected these problems and exhibited the most acceptable physical stability with respect to appearance, particle size distribution, resuspendability, and syringeability of the micronized steroid.
- dispersing and/or wetting agent e.g. 0.2% w/v each of Tween ® 80 (polysorbate 80) and Span ® 40 (sorbitan monopalmitate)
- a symptom of a disease refers to the lessening, decrease, or diminishing of a symptom, state, or condition.
- a symptom of a disease is ameliorated when the symptom decreases in severity of occurrence or effect in a patient.
- a symptom of a disease is ameliorated when the symptom is completely eradicated or eliminated from the patient.
- preventing refers to delaying and/or precluding the onset of a disorder, disease, or condition, and/or its attendant symptom(s); keeping a subject from acquiring a disease; or reducing a subject's risk of acquiring a disorder, disease, or condition.
- treating in relation to the present invention refers to preventing, curing, reversing, attenuating, alleviating, minimizing, suppressing, or halting the deleterious effects of a disease state, disease progression, or other abnormal condition.
- treatment may involve alleviating a symptom (i.e., not necessarily all symptoms) of a disease or attenuating the progression of a disease.
- the improved formulation and process comprises the following steps: Non-sterile, unmicronized LB drug substance first undergoes the process of sterile filtration and recrystallization.
- the process involves dissolving the levonorgestrel butanoate in dichloromethane or another suitable solvent and sterile filtering the solution.
- the levonorgestrel butanoate is then recrystallized from the sterile filtered solution, for example, in a rotary evaporator and washed with ethanol or other suitable solvent to reduce the amount of residual dichloromethane.
- the sterile filtered and recrystallized drug substance is then sterile micronized.
- the sterile micronization process involves reducing the particle size ofthe sterile filtered and recrystallized LB drug substance, such as by milling, under aseptic conditions to yield a median (D50) particle size for the LB that is in the range of 5 - 50 ⁇ , more particularly in the range of 10-30 ⁇ and in other cases in the range of 13 - 35 ⁇ , 13 - 40 ⁇ , 13 - 50 ⁇ , 15 - 35 ⁇ , 15 - 40 ⁇ , 15 - 50 ⁇ , 20 - 35 ⁇ , 20 - 40 ⁇ , or 20 - 50 ⁇ .
- D50 median
- non-sterile unmicronized LB drug substance is first milled (dry or wet) under non-aseptic conditions to yield a median (D50) particle size for the LB that is in the range of 5 - 50 ⁇ followed by sterilization using either gamma or e-beam irradiation to produce the sterile micronized LB drug substance.
- D50 median particle size
- the particle size is in the range of 10-30 ⁇ and in other cases in the range of 13 - 35 ⁇ , 13 - 40 ⁇ , 13 - 50 ⁇ , 15 - 35 ⁇ , 15 - 40 ⁇ , 15 - 50 ⁇ , 20 - 35 ⁇ , 20 - 40 ⁇ , or 20 - 50 ⁇
- non-sterile unmicronized LB drug substance is dissolved in dichloromethane or other suitable solvent followed by evaporation of the solvent by spraying the LB solution into a drying chamber to produce a median (D50) particle size for the LB that is in the range of 5 - 50 ⁇ , more particularly in the range of 10-30 ⁇ and in other cases in the range of 13 - 35 ⁇ , 13 - 40 ⁇ , 13 - 50 ⁇ , 15 - 35 ⁇ , 15 - 40 ⁇ , 15 - 50 ⁇ , 20 - 35 ⁇ , 20 - 40 ⁇ , or 20 - 50 ⁇ .
- the spray dried micronized LB drug substance is then sterilized using either gamma or e-beam irradiation to produce the sterile micronized LB drug substance.
- the sterile micronized LB is then formulated into a sterile aqueous vehicle to form the final sterile injectable suspension product.
- the sterile aqueous vehicle comprises: a wetting agent, a dispersing agent, a thickener, a buffering agent, and a preservative.
- the sterile aqueous vehicle comprises: polysorbate 80 (Tween ® 80), sorbitan monopalmitate (Span ® 40), sodium carboxymethyl cellulose, sodium phosphate dibasic anhydrous, sodium phosphate monobasic dihydrate, and benzyl alcohol.
- manufacturing of the sterile LB injectable suspension is conducted in two parts.
- the first part (Part I) comprises a sterile aqueous solution of a thickener (e.g., sodium carboxymethyl cellulose), buffering agent (e.g., sodium phosphate dibasic anhydrous, sodium phosphate monobasic dihydrate), and a preservative (e.g., benzyl alcohol).
- the second part (Part II) contains a sterile aqueous solution of a wetting agent (e.g., polysorbate 80) and dispersing agent (e.g., sorbitan monopalmitate).
- a wetting agent e.g., polysorbate 80
- dispersing agent e.g., sorbitan monopalmitate
- the Part I solution contributes to approximately 50-95%, more particularly about 60-80%), 70-80%> or 75% of the total batch size of the active suspension while the Part II solution contributes approximately 5-50%, 15-35%), 15-25%) or 20%.
- the sterile micronized levonorgestrel butanoate drug substance is aseptically added into the sterile Part II solution and mixed until dispersed.
- the sterile Part I solution is then aseptically added with mixing to the sterile Part II solution containing the LB to form the final drug product suspension.
- the final drug product suspension is then aseptically homogenized to ensure uniformity of the suspension.
- the final drug product suspension is then aseptically filled into an appropriate container such as a sealed vial or prefilled syringe for final use.
- the process of making the suspension formulation was also modified to improve the blend uniformity and physical stability of the drug product. Specifically, the order of addition of the LB and the formulation components has been modified along with the dispersion/mixing and homogenization of the LB and formulation components.
- the micronized LB is first mixed into a solution containing the wetting and dispersion agents.
- a separate solution is also prepared to dissolve the thickening agent, the buffering agents, and the preservative. These two separate solutions are then mixed together and homogenized to produce a uniform LB suspension product.
- the viscosity of the formulation has been modified to improve the physical stability of the suspension in terms of the settling rate of the LB particles. Slower settling rates are particularly important during the drug product manufacturing process to ensure product consistency and uniformity when holding and transferring the final bulk suspension product for downstream operations such as in-process sampling and testing, filling, etc.
- Fig. 1 shows the results of a settling time study demonstrating that a sodium carboxymethyl cellulose (NaCMC) concentration of 0.5 - 1.0% in the formulation is optimal for minimizing the effects of settling of the LB particles from the suspension.
- NaCMC sodium carboxymethyl cellulose
- Fig. 2 shows the in vitro release data for the improved LB injectable depot formulation micronized to different particle size ranges (Dso), demonstrating longer in vitro release rates for formulations prepared with larger particle sized LB drug substance.
- In vitro release was conducted using a flow through cell in a closed-loop mode with phosphate buffered saline pH 7.4 containing 0.75% sodium lauryl sulfate at 37 °C as the test medium and a flow rate of 20 mL/minute.
- the process of preparing the sterile micronized LB drug substance by sterile filtration and recrystallization followed by sterile micronization can also be improved to increase the efficiency and scalability of this part of the manufacturing process.
- An alternative process for preparing the sterile micronized LB drug substance consists of first subjecting non-sterile, non-micronized LB drug substance to size reduction processes such as dry-milling or wet-milling or spray drying to achieve the desired particle size followed by sterilization of the micronized LB via gamma or e-beam irradiation.
- Example 1 An LB injectable depot suspension formulation comprising the following:
- Example 2 The sterile Part I solution can be prepared by adding a portion ( ⁇ 30%) of cold ( ⁇ 10°C) water for injection (WFI) to a mixing vessel and then adding benzoyl alcohol to the cold WFI in the vessel and stirring for 5 minutes. While mixing, slowly adding sodium carboxymethyl cellulose (NaCMC), medium viscosity fine grade in small aliquots to the vessel and mixing until visually completely dissolved. Once the NaCMC is visually dissolved the remaining WFI (at room temperature) is slowly added to the vessel and the solution is mixed for approximately 1.5 hours. Sodium phosphate dibasic anhydrous is then added to the vessel, while mixing, and the solution is then mixed until dissolved. Sodium phosphate monobasic dihydrate is then added to the vessel, while mixing, and the solution is then mixed until dissolved. The final Part I solution is then sterile filtered to produce a sterile solution.
- WFI cold ( ⁇ 10°C) water for injection
- benzoyl alcohol to the cold WFI in the vessel and stirring for 5 minutes
- Example 3 The sterile Part II solution can be prepared by adding a portion ( ⁇ 87.5%) of WFI to a mixing vessel and then adding polysorbate 80 to the WFI in the vessel and stirring for approximately 20 minutes. Sorbitan monopalmitate is then added to the vessel and the mixture is homogenized at approximately 3000 rpm for a minimum of 45 minutes until the sorbitan monopalmitate is dispersed. Once the sorbitan monopalmitate is dispersed the remaining WFI is added to the vessel and the solution is mixed for a minimum of 10 minutes. The final Part II solution is then autoclaved to produce a sterile solution.
- Example 4 The final sterile LB drug product suspension can be prepared by placing the sterile Part II solution into a sterile mixing vessel in an aseptic environment and then slowly adding, in small portions (approximately 0.5 g per minute), the sterile micronized LB to the sterile Part II solution in the vessel while mixing. Allow the LB to completely disperse after each addition before beginning the next addition. After the final addition of LB continue mixing for an additional 15 - 30 minutes. While mixing, slowly add the sterile Part I solution to the vessel over an approximately 5 minute period. Continue mixing for a minimum of 15 minutes. Q.S. the suspension with WFI and continue mixing for
- sterile LB suspension approximately 30 minutes. Homogenize the final sterile LB suspension at 3500 rpm for a minimum of 2 hours. With continuous mixing, aseptically fill the sterile homogenized LB suspension into an appropriate sterile container (e.g., sealed vial, prefilled syringe, etc.) for final use.
- an appropriate sterile container e.g., sealed vial, prefilled syringe, etc.
- Example 5 A LB injectable depot suspension formulation comprising the same composition as in Example 1 except with the LB micronized via milling or spray drying under non-sterile conditions and then sterilized by e-beam or gamma irradiation.
- Table 2 shows the physical stability data for the improved LB injectable depot suspension formulation containing wetting and/or dispersing agents, Tween ® 80 (polysorbate 80) and Span ® 40 (sorbitan monopalmitate) (0.2% each), demonstrating lack of particle size growth and aggregation of the product over a two year period when stored at 25°C and 65% relative humidity.
- the suspension sediment is easily redispersed with gently swirling and inversion and the redispersed suspension maintains its ability to be withdrawn by a 23-gauge syringe.
- Table 3 shows the results of the modified dispersion/mixing and homogenization processes for the improved manufacturing process for the improved LB injectable depot suspension formulation demonstrating the effectiveness of the dispersion/mixing and homogenization process steps. More specifically, Table 3 shows the uniformity of the LB particle size distribution and concentration following dispersion and mixing of the micronized LB with the formulation components followed by homogenization of the final LB suspension product. The data shows that a uniform mixture is obtained within 15 - 30 minutes of mixing following dispersion of the LB and the formulation components into solution. In addition, the final suspension product continues to maintain its uniformity following 74 - 144 minutes of homogenization.
- Fig. 3 and Fig. 4 show typical particle size distributions and photomicrographs of LB drug substance prepared by dry milling.
- the dry milled LB powder was dispersed in 1% polysorbate 20 and three replicate measurements of the particle size distribution were made. Results for particle size ( ⁇ ) are provided in Table 4.
- Fig. 5 and Fig. 6 show typical particle size distributions and photomicrographs of LB drug substance prepared by wet milling. After wet milling for 15 minutes, the LB suspension was sampled and three replicate measurements of the particle size distribution were made. Results for particle size ( ⁇ ) are provided in Table 5.
- Fig. 7 and Fig. 8 show typical particle size distributions and photomicrographs of LB drug substance prepared by spray drying processes.
- the spray dried LB powder was dispersed in 0.5% polysorbate 80 and three replicate measurements of the particle size distribution were made. Results for particle size ( ⁇ ) are provided in Table 6.
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- Gynecology & Obstetrics (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA3015781A CA3015781C (en) | 2016-02-24 | 2017-02-23 | An improved formulation of long-acting levonorgestrel butanoate injectable depot suspension |
JP2018545362A JP2019506443A (en) | 2016-02-24 | 2017-02-23 | Improved sustained-release injectable depot levonogestrel butanoate for injection |
AU2017223595A AU2017223595B2 (en) | 2016-02-24 | 2017-02-23 | An improved formulation of long-acting levonorgestrel butanoate injectable depot suspension |
US16/079,811 US20190328749A1 (en) | 2016-02-24 | 2017-02-23 | Formulation of long-acting levonorgestrel butanoate injectable depot suspension |
EP17757194.0A EP3419604A4 (en) | 2016-02-24 | 2017-02-23 | An improved formulation of long-acting levonorgestrel butanoate injectable depot suspension |
Applications Claiming Priority (2)
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US201662299257P | 2016-02-24 | 2016-02-24 | |
US62/299,257 | 2016-02-24 |
Publications (1)
Publication Number | Publication Date |
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WO2017147274A1 true WO2017147274A1 (en) | 2017-08-31 |
Family
ID=59686574
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US2017/019092 WO2017147274A1 (en) | 2016-02-24 | 2017-02-23 | An improved formulation of long-acting levonorgestrel butanoate injectable depot suspension |
Country Status (6)
Country | Link |
---|---|
US (1) | US20190328749A1 (en) |
EP (1) | EP3419604A4 (en) |
JP (1) | JP2019506443A (en) |
AU (1) | AU2017223595B2 (en) |
CA (1) | CA3015781C (en) |
WO (1) | WO2017147274A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2023114205A1 (en) * | 2021-12-15 | 2023-06-22 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Levonorgestrel butanoate formulation and methods relating thereto |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0129947A2 (en) * | 1983-05-19 | 1985-01-02 | World Health Organisation | Contraceptive compositions based on esters of levo-norgestrel |
US5360616A (en) * | 1990-06-14 | 1994-11-01 | Applicaciones Farmaceuticas S.A. De C.V. | Injectable pharmaceutical composition |
US20010051656A1 (en) * | 1997-10-28 | 2001-12-13 | Place Virgil A. | Co-administration of a prostaglandin and an androgenic agent in the treatment of female sexual dysfunction |
US20080317844A1 (en) * | 2005-04-15 | 2008-12-25 | Clarus Therapeutics, Inc. | Pharmaceutical Delivery Systems for Hydrophobic Drugs and Compositions Compositions Comprising Same |
US20130018027A1 (en) * | 2010-03-22 | 2013-01-17 | Repros Therapeutics Inc. | Compositions and methods for non-toxic delivery of antiprogestins |
US9168264B2 (en) * | 2011-07-12 | 2015-10-27 | Preglem Sa | Treatment of excessive menstrual bleeding associated with uterine fibroids |
-
2017
- 2017-02-23 CA CA3015781A patent/CA3015781C/en active Active
- 2017-02-23 EP EP17757194.0A patent/EP3419604A4/en active Pending
- 2017-02-23 AU AU2017223595A patent/AU2017223595B2/en active Active
- 2017-02-23 WO PCT/US2017/019092 patent/WO2017147274A1/en active Application Filing
- 2017-02-23 US US16/079,811 patent/US20190328749A1/en active Pending
- 2017-02-23 JP JP2018545362A patent/JP2019506443A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0129947A2 (en) * | 1983-05-19 | 1985-01-02 | World Health Organisation | Contraceptive compositions based on esters of levo-norgestrel |
US5360616A (en) * | 1990-06-14 | 1994-11-01 | Applicaciones Farmaceuticas S.A. De C.V. | Injectable pharmaceutical composition |
US20010051656A1 (en) * | 1997-10-28 | 2001-12-13 | Place Virgil A. | Co-administration of a prostaglandin and an androgenic agent in the treatment of female sexual dysfunction |
US20080317844A1 (en) * | 2005-04-15 | 2008-12-25 | Clarus Therapeutics, Inc. | Pharmaceutical Delivery Systems for Hydrophobic Drugs and Compositions Compositions Comprising Same |
US20130018027A1 (en) * | 2010-03-22 | 2013-01-17 | Repros Therapeutics Inc. | Compositions and methods for non-toxic delivery of antiprogestins |
US9168264B2 (en) * | 2011-07-12 | 2015-10-27 | Preglem Sa | Treatment of excessive menstrual bleeding associated with uterine fibroids |
Non-Patent Citations (6)
Title |
---|
ABUHANOGLU ET AL.: "Radiation sterilization of new drug delivery systems", INTERVENTIONAL MEDICINE & APPLIED SCIENCE, vol. 6, 4 June 2014 (2014-06-04), pages 51 - 60, XP055412065 * |
BEETSMA: "The Differences Between Wetting Agents and Dispersants", PROSPECTOR, 10 April 2015 (2015-04-10), pages 1, XP055412067, Retrieved from the Internet <URL:https://knowledge.ulprospector.com/2282/pc-differences-between-wetting-agents -and-dispersants> * |
COULTAS: "AstraZeneca's pediatric asthma medication patent held invalid as obvious", INTELLECTUAL PROPERTY LAW DAILY, 17 February 2015 (2015-02-17), pages 1 - 3, XP009512362, Retrieved from the Internet <URL:http://www.dailyreportingsuite.com/ip/news/astrazeneca_s_pediatric_asthma_medication_patent_held_invalid_as_obvious> * |
CROSIGNANI ET AL.: "Levonorgestrel-releasing intrauterine device versus hysteroscopic endometrial resection in the treatment of dysfunctional uterine bleeding", OBSTETRICS & GYNECOLOGY, vol. 90, no. 2, 1 January 1997 (1997-01-01), pages 257 - 263, XP055575918, DOI: 10.1016/S0029-7844(97)00226-3 * |
See also references of EP3419604A4 * |
WU ET AL.: "Long-Acting Injectable Hormonal Dosage Forms for Contraception", PHARMACEUTICAL RESEARCH, vol. 32, no. 7, 22 April 2015 (2015-04-22), pages 2180 - 2191, XP035927599 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2023114205A1 (en) * | 2021-12-15 | 2023-06-22 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Levonorgestrel butanoate formulation and methods relating thereto |
Also Published As
Publication number | Publication date |
---|---|
EP3419604A1 (en) | 2019-01-02 |
CA3015781C (en) | 2024-04-23 |
CA3015781A1 (en) | 2017-08-31 |
AU2017223595B2 (en) | 2022-11-24 |
AU2017223595A1 (en) | 2018-10-11 |
EP3419604A4 (en) | 2019-10-09 |
JP2019506443A (en) | 2019-03-07 |
US20190328749A1 (en) | 2019-10-31 |
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