US20180169190A1 - Insulin containing pharmaceutical compositions - Google Patents

Insulin containing pharmaceutical compositions Download PDF

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US20180169190A1
US20180169190A1 US15/843,016 US201715843016A US2018169190A1 US 20180169190 A1 US20180169190 A1 US 20180169190A1 US 201715843016 A US201715843016 A US 201715843016A US 2018169190 A1 US2018169190 A1 US 2018169190A1
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Prior art keywords
pharmaceutical composition
compound
formulation
phenol
cresol
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Inventor
Mathias Norrman
Susanne Hostrup
Dorte Bjerre Steensgaard
Holger Martin Strauss
Rosa Rebecca Erritzoee Hansen
Svend Havelund
Morten Schlein
Jesper Soendergaard Pedersen
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Novo Nordisk AS
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Novo Nordisk AS
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Assigned to NOVO NORDISK A/S reassignment NOVO NORDISK A/S ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HAVELUND, SVEND, HANSEN, ROSA REBECCA ERRITZOEE, HOSTRUP, Susanne, NORRMAN, MATHIAS, PEDERSEN, JESPER SOENDERGAARD, SCHLEIN, MORTEN, STEENSGAARD, DORTE BJERRE, STRAUSS, HOLGER MARTIN
Publication of US20180169190A1 publication Critical patent/US20180169190A1/en
Priority to US16/023,328 priority Critical patent/US10265385B2/en
Priority to US16/280,603 priority patent/US10596231B2/en
Priority to US16/984,990 priority patent/US20200384088A1/en
Priority to US17/692,238 priority patent/US20220202909A1/en
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A61K38/28—Insulins
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A61K38/26—Glucagons
    • 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
    • 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
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones

Definitions

  • the present invention is in the field of pharmaceutical compositions for the treatment of medical conditions relating to diabetes. More specifically the invention provides pharmaceutical compositions comprising a long-acting acylated derivative of a human insulin analogue, and to the medical use of such compositions for basal insulin administration therapy.
  • the primary objective of insulin therapy in the treatment of metabolic disorders is to produce sustained near-normal glycemia by replacing or supplementing endogenous insulin secretion in as physiological a manner as possible, post-prandially as well as between meals and overnight. Separating basal and meal-related (bolus) insulin requirements represents a systematic approach to subcutaneous insulin therapy.
  • Non-covalent zinc mediated oligomerisation is a well-described property of insulin products. Under physiological pH, human insulin is soluble but has a tendency to self-associate into well-defined hexamers (i.e. a unit of six insulin molecules), by coordination of two zinc ions (Zn ++ ) to high affinity (B10His) binding sites. It is also well-known that phenolic ligands, especially phenol, bind specifically to the insulin hexamer and promote R-state hexamer formation. Upon injection, phenolic ligands diffuses quickly from the injection site. In the absence of phenol at the injection site, the conformation and size of the insulin oligomer may change, as well as the viscosity of the insulin-containing solution, contributing to a prolonged action profile.
  • WO 2009/115469 describes various long-acting insulin derivatives with acylated fatty di-acid chains.
  • WO 2013/153000 describes the formulation of those long-acting insulin derivatives for subcutaneous administration, which contains high level of zinc (no less than 3.5 Zn ++ /six moles of insulin derivatives). It was designed in order to obtain the prolonged duration of action commensurate with a once-weekly administration profile. High content of Zn ++ in the formulations described in WO 2009/115469 lead to a prolonged PK profile.
  • WO 2009/063072 discloses pharmaceutical compositions for parenteral administration comprising a basal insulin derivative (e.g. degludec) and a GLP-1 derivative (e.g, liraglutid). Because liraglutide monomer binds with zinc to form di-heptmer, zinc level higher than the degludec mono formulation is necessary in the combo formulation, to achieve comparable PK profile of degludec, and achieve acceptable physical stability.
  • a basal insulin derivative e.g. degludec
  • GLP-1 derivative e.g, liraglutid
  • a new formulation of the long-acting insulin derivatives has been developed, which is capable of promoting a conformational state and oligomerisation pattern more closely resembling that of human insulin, i.e. hexamers, especially R6 hexamers.
  • the invention provides a pharmaceutical composition comprising a selected long-acting insulin derivative in a unique combination of excipients carefully formulated in order to reduce formation of oligomers at the injection site, while still showing PK/PD properties suited for a once-weekly administration.
  • the invention provides a pharmaceutical composition with decreased viscosity upon injection and accordingly decreased propensity to create any discomfort upon injection.
  • the invention provides a pharmaceutical composition with improved stability.
  • the invention provides a pharmaceutical composition for use as a medicament for the treatment of a metabolic disorder.
  • the invention provides pharmaceutical composition comprising an insulin derivative selected from the group consisting of
  • A14E, B25H, desB27, B29K(N ⁇ -Octadecandioyl- ⁇ Glu), desB30 human insulin (Compound 4); and further comprising of from about 1 to about 2% (weight/weight) of glycerol; of from about 45 to about 75 mM of phenol; of from about 0 to about 19 mM of m-cresol; of from about 1.5 to about 2.5 moles of zinc ions per six moles of said insulin derivative; not more than about 75 mM of sodium chloride; and having a pH value in the range of from 7.2 to 8.0.
  • the invention provides pharmaceutical compositions further comprising an insulinotropic GLP-1 compound, and in particular the insulinotropic GLP-1 compound known as semaglutide.
  • Semaglutide may be described by the structure Aib8,Lys26(OEG-OEG-gamma-Glu-C18-diacid),Arg34)GLP-1 H(7-37)-OH, which may also be designated as (N-epsilon26-[2-(2- ⁇ 2-[2-(2- ⁇ 2-[(S)-4-Carboxy-4-(17-carboxyheptadecanoylamino) butyrylamino]ethoxy ⁇ ethoxy)acetylamino]ethoxy ⁇ ethoxy)-acetyl] [Aib8,Arg34]GLP-1-(7-37), c.f. disclosure in WO 2006/097537.
  • a pharmaceutical composition of the invention comprising an insulin derivative, which is A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]acetyl)), desB30 human insulin (Compound 1).
  • a pharmaceutical composition of the invention comprising an insulin derivative, which is A14E, B16H, B25H, B29K(N ⁇ -Hexadecandioyl- ⁇ Glu), desB30 human insulin (Compound 2).
  • a pharmaceutical composition of the invention comprising an insulin derivative, which is A14E, B16H, B25H, B29K(N ⁇ -Eicosanedioyl- ⁇ Glu), desB30 human insulin (Compound 3).
  • a pharmaceutical composition of the invention comprising an insulin derivative, which is A14E, B25H, desB27, B29K(N ⁇ -Octadecandioyl- ⁇ Glu), desB30 human insulin (Compound 4).
  • composition of the previous embodiments comprising of from about 1 to about 2% (weight/weight) of glycerol.
  • composition of the previous embodiments comprising of from about 1.4 to about 1.8% (weight/weight) of glycerol.
  • composition of the previous embodiments comprising about 1.5% or 1.6% (weight/weight) of glycerol.
  • composition of the previous embodiments comprising of from about 45 to about 75 mM of phenol.
  • composition of previous embodiments comprising of from about 50 to about 70 mM of phenol.
  • composition of previous embodiments comprising of from about 55 to about 65 mM of phenol.
  • composition of the previous embodiments comprising about 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, or 70 mM of phenol.
  • composition of the previous embodiments comprising of from about 0 to about 19 mM of m-cresol.
  • composition of the previous embodiments comprising 0 mM, 1 mM, 2 mM, 3 mM, 4 mM of m-cresol.
  • composition of the previous embodiments comprising of from about 0 to about 15 mM of m-cresol.
  • composition of the previous embodiments comprising about 5 mM, 6 mM, 7 mM, 8 mM, 9 mM, 10 mM, 11 mM, 12 mM, 13 mM, 14 mM, 15 mM, 16 mM, 17 mM, 18 mM or 19 mM of m-cresol.
  • composition of the previous embodiments comprising of from about 1.5 to about 2.5 moles of zinc ions per six moles of insulin derivative.
  • composition of the previous embodiments comprising of from about 2.0 to about 2.4 moles of zinc ions per six moles of insulin derivative.
  • composition of the previous embodiments comprising about 2.0 or 2.1 moles of zinc ions per six moles of insulin derivative.
  • composition of the previous embodiments comprising about 2.2 or 2.3 moles of zinc ions per six moles of insulin derivative.
  • composition of the previous embodiments comprising about 2.4 or 2.5 moles of zinc ions per six moles of insulin derivative.
  • composition of the previous embodiments comprising less than about 75 mM of sodium chloride.
  • composition of the previous embodiments comprising of from about 5 to about 50 mM of sodium chloride.
  • composition of the previous embodiments comprising of from about 10 to about 25 mM of sodium chloride.
  • composition of the previous embodiments comprising of from about 15 to about 25 mM of sodium chloride.
  • composition of the previous embodiments comprising about 20 mM, 50 mM or 75 mM of sodium chloride.
  • composition of the previous embodiments which has a pH value in the range of from 7.2 to 8.0.
  • composition of the previous embodiments which has a pH value in the range of from 7.2 to 7.6.
  • composition of the previous embodiments which has a pH value about 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, or 7.9.
  • composition of the previous embodiments comprising of about 4.2 mM of insulin derivative; of from about 1 to about 2% (weight/weight) of glycerol; of from about 45 to about 75 mM of phenol; of from about 0 to about 15 mM of m-cresol; of from about 1.5 to about 2.5 moles of zinc ions per six moles of said insulin derivative; not more than about 50 mM of sodium chloride; and having a pH value in the range of from 7.2 to 8.0.
  • composition of the previous embodiments comprising about 0 mM of m-cresol.
  • composition of the previous embodiments comprising of from about 5 to about 10 mM of m-cresol.
  • composition of the previous embodiments comprising about 10 mM of m-cresol.
  • a pharmaceutical composition comprising A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]-acetyl)), desB30 human insulin (Compound 1); and semaglutide; and further comprising of from about 1 to about 2% (weight/weight) of glycerol; of from about 45 to about 75 mM of phenol; of from 0-15 mM of m-cresol; of from about 1.5 to about 2.5 moles of zinc ions per six moles of said insulin derivative; not more than about 25 mM of sodium chloride; and having a pH value in the range of from 7.2 to 8.0
  • composition according to the previous embodiments comprising from about 0.20 to about 0.70 mM semaglutide.
  • composition according to the previous embodiments comprising from about 0.30 to about 0.70 mM semaglutide.
  • composition comprising from about 3.5 mM to about 5.0 mM A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]-acetyl)), desB30 human insulin (Compound 1).
  • composition comprising from about 0.30 to about 0.70 mM semaglutide, and from about 3.5 mM to about 5.0 mM A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]acetyl)), desB30 human insulin (Compound 1).
  • composition comprising about 0.30 mM semaglutide, and from about 3.5 mM to about 5.0 mM A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]acetyl)), desB30 human insulin (Compound 1).
  • composition comprising about 0.40 mM semaglutide, and 4.2 mM A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]-acetyl)), desB30 human insulin (Compound 1).
  • composition according to the previous embodiments comprising about 0.49 mM or 0.50 mM semaglutide, and 4.2 mM A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)-ethoxy]acetyl)), desB30 human insulin (Compound 1).
  • composition comprising about 0.60 mM semaglutide, and 4.2 mM A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]-acetyl)), desB30 human insulin (Compound 1).
  • a pharmaceutical (coformulation) composition comprising A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ -ethoxy)ethoxy]acetyl)), desB30 human insulin (Compound 1); and semaglutide; and further comprising about 1.5% (weight/weight) of glycerol; of about 60 mM of phenol; about 0 mM of m-cresol; about 2.2 moles of zinc ions per six moles of said insulin derivative; about 20 mM of sodium chloride; and having a pH value of about 7.4.
  • a pharmaceutical (coformulation) composition comprising A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ -ethoxy)ethoxy]acetyl)), desB30 human insulin (Compound 1); and semaglutide; and further comprising about 1.5% (weight/weight) of glycerol; of about 60 mM of phenol; about 10 mM of m-cresol; about 2.2 moles of zinc ions per six moles of said insulin derivative; about 20 mM of sodium chloride; and having a pH value of about 7.4.
  • composition of the previous embodiments for administration to a subject in need hereof at intervals less frequent than once-daily (i.e. at intervals longer than 24 hours), during a period of time of at least 3 months, at least 6 months, or of at least 1 year.
  • composition of the previous embodiments for administration to a subject in need for administration to the subject with a frequency in the range of from every 2 nd day to every 11 th day, on average.
  • composition of the previous embodiments for administration to a subject in need for administration to the subject with a frequency in the range of from every 3 rd day to every 10 th day, on average.
  • composition of the previous embodiments for administration to a subject in need for administration to the subject with a frequency in the range of from every 4 th day to every 9 th day, on average.
  • composition of the previous embodiments for administration to a subject in need for administration to the subject with a frequency in the range of from every 5 th day to every 8 th day, on average.
  • composition of the previous embodiments for administration to a subject in need for administration to the subject with a frequency in the range of from every 6 th day to every 7 th day, on average.
  • composition of the previous embodiments for administration to a subject in need for administration to the subject once a week, i.e. on every 7 th day, on average, during a period of time of at least 3 months, at least 6 months, or of at least 1 year.
  • a method for making injectable pharmaceutical composition comprises:
  • the invention provides pharmaceutical compositions useful as medicaments for the treatment of metabolic diseases, disorders or conditions, and, in particular, diseases, disorders or conditions relating to diabetes.
  • the pharmaceutical composition of the invention is for use in the treatment or alleviation of a disease, disorder or condition relating to diabetes, Type 1 diabetes, Type 2 diabetes, impaired glucose tolerance, hyperglycemia, dyslipidemia, obesity, or metabolic syndrome (metabolic syndrome X, insulin resistance syndrome).
  • a disease, disorder or condition relating to diabetes Type 1 diabetes, Type 2 diabetes, impaired glucose tolerance, hyperglycemia, dyslipidemia, obesity, or metabolic syndrome (metabolic syndrome X, insulin resistance syndrome).
  • the pharmaceutical composition of the invention is for use in the treatment or alleviation of a disease, disorder or condition relating to diabetes, and in particular Type 1 diabetes, or Type 2 diabetes.
  • the actual dosage depends on the nature and severity of the disease being treated, and is within the discretion of the physician, and may be varied by titration of the dosage to the particular circumstances of this invention to produce the desired therapeutic effect.
  • FIG. 1A , FIG. 1B and FIG. 1C show oligomerisation of Compound 1 mono Formulations A, B, and C at simulated injection site conditions:
  • FIG. 1A Apparent average hydrodynamic radius (rH) [nm] measured by DLS;
  • FIG. 1B Apparent average molecular weight measured by CG-MALS
  • FIG. 1C Apparent average sedimentation coefficient (S) measured by AUC;
  • Black bars Compound 1, Formulation A containing 4.5 Zn++ per six insulins (mol:mol);
  • FIG. 2A and FIG. 2B show oligomerisation of Compound 1 mono Formulations 01-06 at simulated injection site conditions:
  • FIG. 2A Apparent average hydrodynamic radius (Rh, avg) [nm] measured by DLS;
  • FIG. 2B Apparent average sedimentation coefficient (S*) measured by AUC
  • FIG. 3A - FIG. 3D show apparent dynamic viscosity [cP] ( FIG. 3A , and FIG. 3C ) and specific viscosity [ ⁇ spec] ( FIG. 3B , FIG. 3D ) of different buffer-exchanged formulations of Compound 1 and interstitial fluid buffer (ISF), as a function of temperature [° C.];
  • FIG. 3A and FIG. 3B Formulation A; Formulation B; Formulation C; ISF buffer;
  • FIG. 3C and FIG. 3D Formulation 02; Formulation 03; Formulation 04; ISF buffer;
  • FIG. 4A and FIG. 4B show conformational state of Compound 1 in formulations:
  • FIG. 4A near-UV CD [ ⁇ 251 nm(M-1 cm-1)] showing conformational changes (T-state; mixed TR state; R-state) as a function of Zn++ per six insulins (mol:mol) for Formulations 01-06;
  • FIG. 4B near-UV CD [ ⁇ 251 nm(M-1 cm-1)] showing conformational changes (T-state; mixed TR state; R-state) as a function of Zn++ per six insulins (mol:mol) for Formulations B1-B6, D1-D7, and human insulin formulations with various zinc level:
  • Human insulin 600 nmol/ml human insulin, 30 mM phenol, 150 mM NaCl, pH 7.4.
  • Black squares Compound 1 formulated with 25 mM phenol, 25 mM m-cresol and 20 mM NaCl;
  • FIG. 5A and FIG. 5B show oligomer distribution of Compound 1 in formulations by SEC:
  • FIG. 5A shows native SEC chromatogram of Formulations 01, 02, 03, 04, 05, and 06;
  • FIG. 5B shows native SEC chromatogram of formulations A and B1-B6
  • FIG. 6A and FIG. 6B show SAXS scattering data [Intensity (a.u.) vs. s( ⁇ -1)] of Compound 1 and human insulin in the formulated state:
  • FIG. 6A Scattering curves of Compound 1 Formulation A shown in black and of human insulin shown in grey (Compound 1, 4.2 mM, 4.5 Zn/hexamer; Human insulin 0.6 mM, 2.2 Zn/hexamer);
  • FIG. 6B Scattering curves of Compound 1 Formulation C shown in black and of human insulin shown in grey (Compound 1, 4.2 mM, 2.2 Zn/hexamer; Human insulin 0.6 mM, 2.2 Zn/hexamer (R6-hexamer));
  • FIG. 7A and FIG. 7B show purity of Compound 1 in formulations:
  • FIG. 7A shows purity (% of total peptide) at 30° C. storage [Time Point (Month)] for Compound 1 Formulation A (black line), Formulation B (grey line) and Formulation C (dotted line);
  • FIG. 7B shows purity (% of total peptide) at 37° C. storage [Time Point (weeks)] for Compound 1 for Formulations 01, 04, 05 and 06;
  • FIG. 8 shows purity of Compound 1 (% of total Compound 1) at 37° C. storage [Time Point (weeks)] in combo formulations with semaglutide:
  • FIG. 9A and FIG. 9B show oligomerisation of combo formulations at simulated injection site conditions:
  • FIG. 9A Apparent average hydrodynamic radius (rH) [nm] measured by DLS;
  • FIG. 9B shows the oligomer size of combo formulations after buffer exchanged as observed by AUC (S*).
  • the API of the formulations is A14E, B16H, B25H, B29K((N ⁇ -Eicosanedioyl- ⁇ Glu-[2-(2- ⁇ 2-[2-(2-aminoethoxy)ethoxy]acetylamino ⁇ ethoxy)ethoxy]acetyl)), desB30 human insulin (Compound 1), obtained as described in e.g. WO 2009/115469, see Example 33.
  • Oligomerisation of Compound 1 was determined at simulated injection site conditions. Simulated injection site conditions were achieved by depletion of phenol and/or metacresol, respectively, and buffer exchange into simulated interstitial fluid buffer. This procedure virtually removed all phenolic ligands but maintained the zinc/insulin ratio of the parent formulation.
  • Formulations are buffer-exchanged into interstitial fluid (ISF-) buffer via PD-MidiTrap G-25 column according to the manufacturers protocol.
  • ISF- interstitial fluid
  • the columns are equilibrated with the target buffer by washing the column with a sufficient volume of target buffer, and the formulation is applied in a suitable volume and eluted with target buffer.
  • the ISF buffer consists of 140 mM NaCl, 4 mM KCl, 1 mM MgSO4, 2 mM CaCl2, 10 mM Hepes, pH 7.4.
  • r H Apparent average hydrodynamic radius was measured by Dynamic Light Scattering (DLS), using a DynaPro PRTM (Wyatt technology, Santa Barbara, Calif., USA). Before analysis samples were centrifuged for 5 minutes at 1200 rpm to remove any dust particles in the solution. Measurements were conducted at 25° C. using 40 acquisitions and 2 sec acquisition time.
  • CG-MALS Composition-Gradient, Multi-Angle Static Light Scattering
  • Sedimentation velocity (SV) experiments were performed with an XL-I Analytical Ultracentrifuge (BeckmanCoulter, Brea, Calif.) in 12-mm or 3-mm double-sector centrepieces capped with sapphire windows. Samples were spun at 40000 rpm and 20° C. until sedimentation was completed and monitored with the interference optics of the instrument. Sedimentation Coefficient Distributions (SCD) were calculated with SedFit, version 11.8 (www.analyticalultracentrifugation.com) using the c(s) model with a grid of 100 s-values over a range sufficient to describe all sedimenting material, as judged by the rmsd and the residual run pattern.
  • SCD Sedimentation Coefficient Distributions
  • the frictional ratio f/fo was treated as a variable to be optimized during fitting (P Schuck, M A Perugini, N R Gonzales, G J Howlett and D Schubert: Size-distribution analysis of proteins by analytical ultracentrifugation: strategies and application to model systems; ( Biophys. J. 2002 82:1096). Average sedimentation coefficient values were obtained via integration of the resulting c(s)-distributions.
  • Temperature-dependent dynamic viscosities were measured with a Lovis2000 rolling-ball type viscosimeter (Anton Paar, Graz, Austria). The temperature was decreased from 40° C. to 4° C. in 2° C. steps, allowing 5 minutes of temperature equilibration between steps. The density of the buffer was simultaneously measured with a DMA5000 densitometer, also from Anton Paar.
  • Formulation A representative of the prior art (see e.g. WO 2013/153000), and Formulations B, C representative of the invention (60 mM phenol/10 mM m-cresol), were prepared.
  • Formulation 01 (same as Formulation A), and Formulations 02, 03, 04, 05 and 06 representative of the invention, were made (Table 1B).
  • the zinc content has been varied from 4.5 Zn ++ /six insulins to 2.4, 2.2, and 2.0 Zn ++ /six insulins.
  • preservative systems of either 25/25 mM phenol/m-cresol or 60/0 mM phenol/m-cresol have been tested.
  • the zinc content was decreased from 4.5 Zn++/six insulins in Formulation A to 2.4 and 2.2 Zn ++ /six insulins in formulations B and C (with increased phenol and decreased metacresol) respectively.
  • This decrease in zinc was accompanied by a reduction of oligomer size (see FIGS. 1A, 1B and 1C ) as determined at simulated injection site conditions by the method described above.
  • Results from formulation 01-06 further confirm that the oligomer size is reduced when Zn is reduced from 4.5 Zn++/six insulins to 2.2 ⁇ 0.2 Zn++/six insulins.
  • the oligomer size is further reduced when phenol/cresol is reduced from 25 mM/25 mM to 60 mM/0 mM. See FIGS. 2A and 2B .
  • t max represents the time to maximum concentration (maximal plasma exposure)
  • t 1/2 represents the elimination half-life in which half of the compound disappears from plasma following administration.
  • Example 1 The altered biophysical properties described in Example 1 are consistent with a PK profile exhibiting earlier t max in pigs (see Table 3). This indicates that the residence time of Compound 1 in the sub-cutis is reduced when formulated according to the invention, and in contrast to the same compound being provided in a formulation according to the prior art.
  • the reduced zinc level almost has no impact on the duration of action (i.e. elimination t 112 is not affected), which makes the formulation according to the invention and the formulation of the prior art equally suited for once-weekly administration.
  • Compound 1 when formulated according to the invention, forms smaller oligomers at the site of injection resulting in a PK/PD profile with a shorter residence time in the sub-cutis (decreased t max ).
  • human insulin exists as hexamers in formulation.
  • Human insulin hexamers can adopt two different conformational states depending on the conformation of the monomers.
  • the eight N-terminal amino acid residues of the insulin monomer B-chain can be in either an extended conformation (T-state) or an ⁇ -helical conformation (R-state).
  • T-state extended conformation
  • R-state ⁇ -helical conformation
  • human insulin adopts the R conformation, which is the favourable conformation with regards to physical and chemical stability (Dunn M F. Zinc-ligand interactions modulate assembly and stability of the insulin hexamer: A review. Biometals 2005; 18; 295-303).
  • FIG. 4A shows the conformational changes (T-state; mixed TR state; R-state) as a function of Zn ++ per six insulins (mol:mol) for formulations 01-06.
  • FIG. 4B shows conformational changes (T-state; mixed TR state; R-state) as a function of Zn++ per six insulins (mol:mol) for Series B and Series D formulations, and human insulin formulatoins.
  • formulations 01-06 show that R-state of Compound 1 in the formulations is are further enriched by decreasing Zn from 4.5 to 2.2Zn ⁇ 0.2Zn/6 Compound 1 and by omitting m-cresol ( FIG. 4A ).
  • Size Exclusion Chromatography is a sensitive method for quantifying the non-covalent oligomer distribution of insulin formulations.
  • SEC was conducted using a BEH200 column, 1.7 ⁇ m 4.6 ⁇ 150 mm with a running buffer consisting of 8.0 mM phenol, 140 mM NaCl, 10 mM Tris-HCl, pH 7.4. Chromatography was conducted at 22 C using 2 ⁇ L injection volume and a flow of 0.3 ml/min.
  • molecular weight standards albumin, a covalent insulin hexamer, and a monomeric insulin were used.
  • Chromatograms were analysed by integration to represent species larger than hexamer (3.0-3.8 min), hexamer (3.8-4.3 min), and species smaller than hexamer (4.3-5.5 min). Please note that exact integration limits for each data set will vary slightly due to variations in column performance.
  • SAXS Small angle X-ray scattering
  • SEC data of Formulations 01-06 show that the oligomer distribution of Compound 1 Formulation 01 is characterised by broad bands with no clear dominant oligomer species.
  • the oligomer distribution of Compound 1 in Formulations 03-06 is narrower compared to Formulations 01 and 02.
  • the retention time of the main peak Formulations 03-06 is consistent with a hexamer and the small peak with a retention time of 5 minutes is consistent with a monomer or dimer.
  • SEC data of Formulations B1-B6 and A (Table 7, FIG. 5B ) also show that with 2.0-2.5 zinc/6 insulins, the hexamer peak is enriched, compared to 4.0 or 4.5 Zn.
  • the hexamer peak is enriched at low zinc (e.g., 2.0Zn to 2.5Zn) compared to high zinc (e.g. 4.0 or 4.5Zn).
  • low zinc e.g. 2.0Zn to 2.5Zn
  • high zinc e.g. 4.0 or 4.5Zn
  • the hexamer is enriched at 60 mM/0 or 10 mM phenol/m-cresol relative to 25/25 mM phenol/m-cresol.
  • the hexamer content is increased and the oligomerisation becomes more well-defined.
  • SAXS data also confirm that the oligomerisation pattern of Compound 1 Formulation A with 4.5 Zn++/hexamer does not resemble the classical human insulin hexamer while a hexamer-based structure of the Compound 1 is dominant in Formulation C ( FIG. 6 ).
  • Formulation C When formulated according to the invention (Formulation C) the oligomerisation pattern becomes more well-defined and consistent with a hexamer based structure similar to human insulin.
  • Purity was determined by reversed phase ultra-high performance liquid chromatography (RP-UHPLC) where the samples were analysed using a Acquity CSH Fluoro Phenyl, 130 ⁇ , 1.7 ⁇ m, 2.1 ⁇ 150 mm column, gradient elution by acetonitrile in a mobile phase of acetonitrile and phosphoric buffer in water with subsequent UV detection (215 nm) under a flow of 0.30 ml/min with a sample injection volume of 2-3 ⁇ l. Purity was evaluated as the area of the main peak divided by the area of all peaks ⁇ 100%.
  • the stability measured as (%) purity of total peptide with RP-UHPLC shows an significantly increased stability of Compound 1 in Formulation B and Formulation C, which comprised 60 mM phenol and 10 mM m-cresol, compared to Compound 1 Formulation A, which comprised 25 mM phenol and 25 mM m-cresol. See Table 8 and FIG. 7A .
  • the stability of formulations presented in table 9 measured as % purity of total peptide with RP-UHPLC further confirms that the chemical stability of Compound 1 increases as a function of zinc concentration in formulations with relatively high level of phenol and low level of m-cresol.
  • the results show an increased stability of Compound 1 when zinc was decreased from 4.5 Zn ++ /six insulins to 2.4, 2.2 and 2.0 Zn ++ /six insulins in formulations with a change in preservative system from 25/25 mM phenol/m-cresol to 60 mM phenol and 0 m-cresol. See Table 9 and FIG. 7B .
  • the Compound 1 formulations were tested in a 96-well microtiter plate with 4 replica of 200 ⁇ l.
  • ThT thioflavin T
  • Thioflavin T (ThT) assay for propensity to form amyloid fibrils was performed on Thermo Fluoroskan, 960 rpm shaking, 37° C., for 45 hours.
  • ThT emission was scanned before and after assay. The lag time until on-set of ThT fluorescence emission is a measurement of physical stability. Lag times were determined from fluorescence curves averaged over 4 replica. A longer lag-time is indicative of higher physical stability.
  • ThT results obtained from the described protocol may vary between experiments. Therefore it is desirable that measurements for a given set of formulations be compared within the same experiment and not across experiments.
  • the same reference formulation was tested together with various formulations of the invention in different experiments. For example, Formulation A vs. Formulation C; Formulation 01 vs. Formulations 04-06.
  • the lag-times obtained in the ThT assay indicates that the physical stability of Compound 1 is improved in formulations with low level of zinc, high level of phenol, and low level of m-cresol.
  • the data showed that when decreasing zinc from 4.5Zn/6Ins to 2.2 ⁇ 0.2Zn/6Ins and concomitant increasing phenol from 25 mM to 60 mM and decreasing m-cresol from 25 mM to 10 mM lead to longer lag time and thus improved physical stability. With m-cresol being removed, the physical stability of Compound 1 was further improved in formulations with low zinc level (see Table 10B).
  • Compound 1 may be co-formulated together with the once-weekly GLP-1 analogue semaglutide for a fixed-ratio combination.
  • ThT thioflavin T
  • Thioflavin T (ThT) assay for propensity to form amyloid fibrils was performed on Thermo Fluoroskan, 960 rpm shaking, 37° C., for 45 hours. ThT emission was scanned before and after assay. The lag time until on-set of ThT fluorescence emission (formation of amyloid fibrils) is a measurement of physical stability. Lag times were determined from fluorescence curves averaged over 8 replica. Lag times were tested twice for combo formulations 1-4 and combo formulations 5 and 6, respectively; and each with mono formulation tested as a reference, to make the results comparable. A longer lag-time is indicative of higher physical stability.
  • the Compound 1 mono-formulation reference and the combo-formulations were tested in a 96-well microtiter plate Thioflavin T (ThT) assay for propensity to form amyloid fibrils.
  • Thioflavin T Thioflavin T
  • the ThT assay indicated that without increasing zinc level, combo formulations of Compound 1 and semaglutide did not compromise the physical stability of Compound 1 compared to that of the Compound 1 mono-formulation. In fact, the lag times of the combo-formulations were much longer than that of the Compound 1 mono-formulation, showing the co-formulating of Compound 1 with semaglutide in fact stabilizes the formulation towards the unwanted amyloid fibril formation. Compared with combo-formulation of other long acting insulin derivative and GLP-1 derivative (e.g. degludec and liraglutide), this finding is unexpected and surprising.
  • other long acting insulin derivative and GLP-1 derivative e.g. degludec and liraglutide
  • Table 14C results show that lowering the level of m-cresol can further improve the physical stability of the combo-formulation of Compound 1 and semaglutide; and increasing the level of phenol also improves the physical stability of the combo-formulation of Compound 1 and semaglutide.
  • Table 14C results also show that when co-formulating Compound 1 with semaglutide in a formulation according to the invention, the physical stability of Compound 1 increases, compared to using prior art formulation (Formulation I) for combo-formulation of Compound 1 and semaglutide.
  • Purity was determined by reversed phase ultra-high performance liquid chromatography (RP-UHPLC) where the samples were analysed using a Acquity CSH Fluoro Phenyl, 130 ⁇ , 1.7 um, 2.1 ⁇ 150 mm column, gradient elution by acetonitrile in a mobile phase of acetonitrile and phosphoric buffer in water with subsequent UV detection (215 nm) under a flow of 0.30 ml/min with a sample injection volume of 2-3 ⁇ l. Purity was evaluated as the area of the main peak divided by the area of all peaks ⁇ 100%.
  • the PK parameters for Compound 1 when co-formulated with semaglutide in Combo 1 and Combo 2 were not significantly changed compared to Compound 1 administrated as a mono-formulation.
  • the t max values were slightly lower for the co-formulations, but with the standard deviation for the Compound 1 reference the values are overlapping.
  • the t 1/2 and MRT were very similar for Compound 1 in the co-formulations compared to the reference mono-formulation. In conclusion the PK properties of Compound 1 were not significantly impacted by the co-formulation with semaglutide.
  • the average size of oligomers formed from combo-formulations at simulated injection site conditions is significantly reduced in formulations with low level of zinc (e.g., 2.4 and 2.2 Zn++/six insulins) compared to formulations with high level zinc (e.g. 4.5 Zn++/six insulin).
  • low level of zinc e.g., 2.4 and 2.2 Zn++/six insulins
  • high level zinc e.g. 4.5 Zn++/six insulin

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BR112022011291A2 (pt) 2019-12-10 2022-09-06 Sanofi Sa Método para formar um conjugado de uma sulfonamida e um polipeptídeo
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US10265385B2 (en) 2016-12-16 2019-04-23 Novo Nordisk A/S Insulin containing pharmaceutical compositions
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