US20030119734A1 - Stable formulation of modified GLP-1 - Google Patents
Stable formulation of modified GLP-1 Download PDFInfo
- Publication number
- US20030119734A1 US20030119734A1 US10/185,923 US18592302A US2003119734A1 US 20030119734 A1 US20030119734 A1 US 20030119734A1 US 18592302 A US18592302 A US 18592302A US 2003119734 A1 US2003119734 A1 US 2003119734A1
- Authority
- US
- United States
- Prior art keywords
- glp
- compound
- formulation
- concentration
- present
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/605—Glucagons
-
- 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
- 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
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/183—Amino acids, e.g. glycine, EDTA or aspartame
-
- 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
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/08—Solutions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P3/08—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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- 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
- A61K9/0043—Nose
-
- 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
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
Definitions
- the present invention relates to pharmaceutical formulations comprising GLP-1 compounds, uses thereof and methods for preparing said formulations.
- the hormones regulating insulin secretion belong to the so-called enteroinsular axis, designating a group of hormones, released from the gastrointestinal mucosa in response to the presence and absorption of nutrients in the gut, which promote an early and potentiated release of insulin.
- the enhancing effect on insulin secretion, the so-called incretin effect is probably essential for a normal glucose tolerance.
- Many of the gastrointestinal hormones, including gastrin and secretin (cholecystokinin is not insulinotropic in man), are insulinotropic, but the only physiologically important ones, those that are responsible for the incretin effect, are the glucose-dependent insulinotropic polypeptide, GIP, and glucagon-like peptide-1(GLP-1).
- GIP insulin dependent diabetes mellitus
- NIDDM non insulin-dependent diabetes mellitus
- GLP-1 a product of the proglucagon
- GLP-1 is one of the youngest members of the secretin-VIP family of peptides, but is already established as an important gut hormone with regulatory function in glucose metabolism and gastrointestinal secretion and metabolism.
- the glucagon gene is processed differently in the pancreas and in the intestine.
- glucagon In the pancreas, the processing leads to the formation and parallel secretion of 1) glucagon itself, occupying positions 33-61 of proglucagon (PG); 2) an N-terminal peptide of 30 amino acids (PG (1-30)) often called glicentin-related pancreatic peptide, GRPP; 3) a hexapeptide corresponding to PG (64-69); 4) and, finally, the so-called major proglucagon fragment (PG (72-158)), in which the two glucagon-like sequences are buried.
- PG glicentin-related pancreatic peptide
- PG major proglucagon fragment
- GLP-1 and analogues of GLP-1 and fragments thereof are potentially useful i.a. in the treatment of type 1 and type 2 diabetes.
- solubility limitations and the low stability against the actions of endogenous diaminopeptidyl peptidase limits the usefulness of these compounds, and thus there still is a need for improvements in this field.
- WO 99/43341 are disclosed certain pharmaceutical formulations comprising GLP-1 having a lipophilic substituent. All of the disclosed formulations are maintained at pH 7.4.
- WO 00/37098 are disclosed shelf-stable formulations comprising GLP-1, a preservative, and a tonicity modifier, at pH 8.2 to 8.8.
- Human GLP-1 is a 37 amino acid residue peptide originating from preproglucagon which is synthesised i.a. in the L-cells in the distal ileum, in the pancreas and in the brain. Processing of preproglucagon to give GLP-1(7-36)amide, GLP-1(7-37) and GLP-2 occurs mainly in the L-cells. A simple system is used to describe fragments and analogues of this peptide. Thus, for example, Val 8 -GLP-1(7-37) (or Val8GLP-1(7-37)) designates a fragment of GLP-1 formally derived from GLP-1 by deleting the amino acid residues Nos.
- Lys 34 (N ⁇ -tetradecanoyl)-GLP-1(7-37) designates GLP-1(7-37) wherein the ⁇ -amino group of the Lys residue in position 34 has been tetradecanoylated.
- amino acid sequence of GLP-1(7-37) is given below, wherein the N-terminal His is no. 7 and the C-terminal Gly is no. 37:
- modified GLP-1 or analogues thereof when formulated in aqueous solution together with a buffer, are physically stable at high concentrations of the modified GLP-1 or analogues thereof, when kept in the pH range from about 7 to about 10.
- the present formulations are physically stable within a given shelf life period at the recommended storage temperature (typically 2-3 years at 2-8° C.).
- the present formulations are physically stable during in-use (typically 1 month at accelerated temperatures e.g. 25° C. or 37° C.).
- the formulations of the invention are also chemically stable thus rendering them shelf-stable and suitable for invasive (eg.
- One object of the present invention is to provide a pharmaceutical formulation comprising a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10;
- Another object of the present invention is to provide a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the formulation contains a GLP-1 compound in a concentration from 1 mg/ml to 100 mg/ml.
- the formulation has a pH from 7.5 to 10.
- the GLP-1 compound is Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37).
- the invention relates to a pharmaceutical formulation comprising a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10;
- the invention in another aspect relates to a pharmaceutical formulation comprising a GLP-1compound, and a buffer, wherein said GLP-1 compound is GLP-1 (7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10;
- the invention relates to a pharmaceutical formulation comprising a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a pharmaceutical formulation comprising a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a pharmaceutical formulation comprising a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a pharmaceutical formulation comprising a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising prepararing a formulation containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising prepararing a formulation containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising prepararing a formulation containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, water, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, water, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, water, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.5 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, water, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.5 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.5 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.5 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10; provided that if an isotonic agent is present and pH is 7.4 then mannitol or NaCl is not the isotonic agent.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparing a formulation containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10; provided that if an isotonic agent is present and pH is 7.4 then mannitol or NaCl is not the isotonic agent.
- the pharmaceutical formulation is an aqueous formulation, i.e. a formulation comprising water. Such formulation is typically a solution or a suspension.
- the pharmaceutical formulation is an aqueous solution.
- aqueous formulation is defined as a formulation comprising at least 50% w/w water.
- aqueous solution is defined as a solution comprising at least 50% w/w water
- aqueous suspension is defined as a suspension comprising at least 50% w/w water.
- the pharmaceutical formulation is a freeze-dried formulation, whereto the physician or the patient adds the solvent prior to use.
- the invention relates to a pharmaceutical formulation
- a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a pharmaceutical formulation
- a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a pharmaceutical formulation
- a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a pharmaceutical formulation
- a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a pharmaceutical formulation
- a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10; provided that if an isotonic agent is present and pH is 7.4 then mannitol or NaCl is not the isotonic agent.
- the invention relates to a pharmaceutical formulation
- a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10; provided that if an isotonic agent is present and pH is 7.4 then mannitol or NaCl is not the isotonic agent.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparation of an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparation of an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml or above, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparation of an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparation of an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparation of an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10; provided that if an isotonic agent is present and pH is 7.4 then mannitol or NaCl is not the isotonic agent.
- the invention relates to a method of preparing a physically stable pharmaceutical formulation of a GLP-1 compound wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof, wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, comprising preparation of an aqueous solution containing the GLP-1 compound, and a buffer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10; provided that if an isotonic agent is present and pH is 7.4 then mannitol or NaCl is not the isotonic agent.
- the present invention relates to a method of reducing blood glucose levels, treating diabetes type I, diabetes type II, obesity, or inhibiting gastric acid secretion, inhibiting apoptosis of ⁇ -cells, or stimulating the proliferation of ⁇ -cells, comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of reducing blood glucose levels, treating diabetes type I, diabetes type II, obesity, or inhibiting gastric acid secretion, inhibiting apoptosis of ⁇ -cells, or stimulating the proliferation of ⁇ -cells
- a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of treating gastric ulcers comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of treating gastric ulcers comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of treating myocardial infarct comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of treating myocardial infarct comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of treating impaired glucose tolerance (IGT) comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- ITT impaired glucose tolerance
- the present invention relates to a method of treating impaired glucose tolerance (IGT) comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- ITT impaired glucose tolerance
- the present invention relates to a method of reducing body weight in a subject in need of body weight reduction comprising administering to the subject an effective amount sufficient to cause reduction in body weight for a period of time effective to produce weight loss, said time being at least 4 weeks, of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of reducing body weight in a subject in need of body weight reduction comprising administering to the subject an effective amount sufficient to cause reduction in body weight for a period of time effective to produce weight loss, said time being at least 4 weeks, of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of treating dyslipidemia, stroke, left ventricular hypertrophy, arrhythmia, bacteraemia, septicaemia, irritable bowel disease, functional dyspepsia, comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- the present invention relates to a method of treating dyslipidemia, stroke, left ventricular hypertrophy, arrhythmia, bacteraemia, septicaemia, irritable bowel disease, functional dyspepsia, comprising administering to a patient in need thereof an effective amount of a pharmaceutical formulation comprising an aqueous solution of a GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10.
- an effective amount is the effective dose to be determined by a qualified practitioner, who may titrate dosages to achieve the desired response. Factors for consideration of dose will include potency, bioavailability, desired pharmacokinetic/pharmacodynamic profiles, condition of treatment (e.g. diabetes, obesity, weight loss, gastric ulcers), patient-related factors (e.g. weight, health, age, etc.), presence of co-administered medications (e.g. insulin), time of administration, or other factors known to a medical practitioner.
- condition of treatment e.g. diabetes, obesity, weight loss, gastric ulcers
- patient-related factors e.g. weight, health, age, etc.
- co-administered medications e.g. insulin
- time of administration or other factors known to a medical practitioner.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for reducing blood glucose levels.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for reducing blood glucose levels.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating diabetes type I.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating diabetes type I.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating diabetes type II.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating diabetes type II.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1 (7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating obesity.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating obesity.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for reducing body weight, typically for reducing body weight in a type 2 diabetic subject.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for reducing body weight, typically for reducing body weight in a type 2 diabetic subject.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating gastric ulcers.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for treating gastric ulcers.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 0.1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for inhibition of apoptosis of ⁇ -cells.
- the present invention relates to use of a GLP-1 compound for the preparation of a pharmaceutical formulation comprising an aqueous solution of the GLP-1 compound, and a buffer, wherein said GLP-1 compound is GLP-1(7-37) or an analogue thereof wherein an amino acid residue of the parent peptide has a lipophilic substituent attached optionally via a spacer, wherein said GLP-1 compound is present in a concentration from 1 mg/ml to 100 mg/ml, and wherein said formulation has a pH from 7.0 to 10, for inhibition of apoptosis of ⁇ -cells.
- treatment is defined as the management and care of a patient, e.g. a mammal, in particular a human, for the purpose of combating the disease, condition, or disorder and includes the administration of a GLP-1 compound to prevent the onset of the symptoms or complications, or alleviating the symptoms or complications, or eliminating the disease, condition, or disorder.
- Pharmaceutical compositions containing a GLP-1 compound according to the present invention may be administered parenterally to patients in need of such a treatment. Parenteral administration may be performed by subcutaneous, intramuscular or intravenous injection by means of a syringe, optionally a pen-like syringe. Alternatively, parenteral administration can be performed by means of an infusion pump.
- compositions which may be a solution or suspension for the administration of the GLP-1 compound in the form of a nasal or pulmonal spray are also be adapted to transdermal administration, e.g. from a patch, optionally a iontophoretic patch, or transmucosal, e.g. bucal, administration.
- a pharmaceutical formulation is found to be physically unstable when it exhibits turbidity.
- a pharmaceutical formulation of GLP1(7-37) is found to be physically unstable as it turns out to be turbid momentaneously after preparation, whereas the same pharmaceutical formulation comprising a GLP-1 compound, for example Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), is found to be physically stable for more than 90 days at 5° C.
- Some of the present formulations are physically stable for more than 11 months and for more than 22 months at 5° C.
- Physical stability of the formulations is evaluated by means of visual inspection and turbidity after storage of the formulation at different temperatures in top filled glass cartridges for various time periods.
- Visual inspection of the formulations is performed in a sharp focused light with a dark background.
- the turbidity of the formulation is characterized by a visual score ranking the degree of turbidity from 0 to 3 (a formulation showing no turbidity corresponds to a visual score 0, and a formulation showing visual turbidity in daylight corresponds to visual score 3).
- a formulation is classified physical unstable with respect to protein aggregation, when it shows visual turbidity in daylight.
- the pharmaceutical formulation comprising the GLP-1 compound is physically stable for more than 12 weeks and for more than 15 months at 5° C. as measured by visual inspection.
- the pharmaceutical formulation comprising the GLP-1 compound is physically stable for more than 12 weeks at 25° C. as measured by visual inspection.
- the pharmaceutical formulation comprising the GLP-1 compound is physically stable for more than 12 weeks at 37° C. as measured by visual inspection.
- the formulation has a pH in the range from 7.5 to 10. In another embodiment of the invention the formulation has a pH in the range from 7.5 to 9.5. In a further embodiment of the invention the formulation has a pH in the range from 7.0 to 9.5. In a further embodiment of the invention the formulation has a pH in the range from 7.0 to 8.0. In a further embodiment of the invention the formulation has a pH in the range from 7.5 to 8.0. In a further embodiment of the invention the formulation has a pH in the range from 9.0 to 10.
- the buffer is selected from the group consisting of sodium acetate, sodium carbonate, citrate, glycylglycine, histidine, glycine, lysine, arginin, sodium dihydrogen phosphate, disodium hydrogen phosphate, sodium phosphate, and tris(hydroxymethyl)-aminomethan, or mixtures thereof.
- the buffer is glycylglycine, sodium dihydrogen phosphate, disodium hydrogen phosphate, sodium phosphate or mixtures thereof.
- the GLP-1 compound is present in a concentration from 0.1 mg/ml to 80 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 1 mg/ml to 80 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 0.1 mg/ml to 50 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 1 mg/ml to 50 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 0.1 mg/ml to 20 mg/ml.
- the GLP-1 compound is present in a concentration from 1 mg/ml to 20 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 0.1 mg/ml to 10 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 1 mg/ml to 10 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 0.1-5 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 1-5 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 0.1-0.5 mg/ml. In a further embodiment of the invention the GLP-1 compound is present in a concentration from 0.6-1 mg/ml. Each one of these specific concentration ranges constitutes an alternative embodiment of the invention.
- the formulation further comprises a pharmaceutically acceptable preservative.
- the preservative is selected from the group consisting of phenol, m-cresol, methyl p-hydroxybenzoate, propyl p-hydroxybenzoate, 2-phenoxyethanol, butyl p-hydroxybenzoate, 2-phenylethanol, benzyl alcohol, chlorobutanol, and thiomerosal, or mixtures thereof.
- the preservative is phenol or m-cresol.
- the preservative is present in a concentration from 0.1 mg/ml to 20 mg/ml. In a further embodiment of the invention the preservative is present in a concentration from 0.1 mg/ml to 5 mg/ml. In a further embodiment of the invention the preservative is present in a concentration from 5 mg/ml to 10 mg/ml. In a further embodiment of the invention the preservative is present in a concentration from 10 mg/ml to 20 mg/ml. Each one of these specific concentration ranges constitutes an alternative embodiment of the invention.
- the formulation further comprises an isotonic agent.
- the isotonic agent is selected from the group consisting of a salt (e.g. sodium chloride), a polyhydric alcohol (e.g. propyleneglycol, xylitol, mannitol, sorbitol or glycerol), a monosaccharide (e.g. glucose or maltose), a disccharide (e.g. sucrose), an amino acid (e.g.
- the isotonic agent is selected from the group consisting of sodium chloride, glycerol, mannitol, glucose, sucrose, L-glycine, L-histidine, arginine, lysine or mixtures thereof. Each one of these specific isotonic agents constitutes an alternative embodiment of the invention.
- the isotonic agent is mannitol or glycerol.
- the isotonic agent is present in a concentration from 1 mg/ml to 50 mg/ml. In a further embodiment of the invention the isotonic agent is present in a concentration from 1 mg/ml to 7 mg/ml. In a further embodiment of the invention the isotonic agent is present in a concentration from 8 mg/ml to 16 mg/ml. In a further embodiment of the invention the isotonic agent is present in a concentration from 17 mg/ml to 50 mg/ml. Each one of these specific concentration ranges constitutes an alternative embodiment of the invention.
- the formulation further comprises a chelating agent.
- the chelating agent is selected from salts of ethlenediaminetetraacetic acid (EDTA), citric acid, and aspartic acid, and mixtures thereof. Each one of these specific chelating agents constitutes an alternative embodiment of the invention.
- the chelating agent is present in a concentration from 0.1 mg/ml to 5 mg/ml. In a further embodiment of the invention the chelating agent is present in a concentration from 0.1 mg/ml to 2 mg/ml. In a further embodiment of the invention the chelating agent is present in a concentration from 2 mg/ml to 5 mg/ml.
- the formulation further comprises a stabiliser selected from the group of high molecular weight polymers or low molecular compounds.
- the stabilizer is selected from polyethylene glycol (e.g. PEG 3350), polyvinylalcohol (PVA), polyvinylpyrrolidone, carboxymethylcellulose, different salts (e.g. sodium chloride), L-glycine, L-histidine, imidazole, arginine, lysine, isoleucine, aspartic acid, tryptophan, threonine and mixtures thereof.
- PEG 3350 polyethylene glycol
- PVA polyvinylalcohol
- polyvinylpyrrolidone polyvinylpyrrolidone
- carboxymethylcellulose different salts (e.g. sodium chloride)
- the high molecular weight polymer is present in a concentration from 0.1 mg/ml to 50 mg/ml. In a further embodiment of the invention the high molecular weight polymer is present in a concentration from 0.1 mg/ml to 5 mg/ml. In a further embodiment of the invention the high molecular weight polymer is present in a concentration from 5 mg/ml to 10 mg/ml. In a further embodiment of the invention the high molecular weight polymer is present in a concentration from 10 mg/ml to 20 mg/ml. In a further embodiment of the invention the high molecular weight polymer is present in a concentration from 20 mg/ml to 30 mg/ml. In a further embodiment of the invention the high molecular weight polymer is present in a concentration from 30 mg/ml to 50 mg/ml.
- the low molecular weight compound is present in a concentration from 0.1 mg/ml to 50 mg/ml. In a further embodiment of the invention the low molecular weight compound is present in a concentration from 0.1 mg/ml to 5 mg/ml. In a further embodiment of the invention the low molecular weight compound is present in a concentration from 5 mg/ml to 10 mg/ml. In a further embodiment of the invention the low molecular weight compound is present in a concentration from 10 mg/ml to 20 mg/ml. In a further embodiment of the invention the low molecular weight compound is present in a concentration from 20 mg/ml to 30 mg/ml. In a further embodiment of the invention the low molecular weight compound is present in a concentration from 30 mg/ml to 50 mg/ml.
- the formulation further comprises a surfactant.
- the surfactant is selected from a detergent, ethoxylated castor oil, polyglycolyzed glycerides, acetylated monoglycerides, sorbitan fatty acid esters, poloxamers, such as 188 and 407, polyoxyethylene sorbitan fatty acid esters, polyoxyethylene derivatives such as alkylated and alkoxylated derivatives (tweens, e.g.
- Tween-20, or Tween-80 monoglycerides or ethoxylated derivatives thereof, diglycerides or polyoxyethylene derivatives thereof, glycerol, cholic acid or derivatives thereof, lecithins, alcohols and phospholipids, glycerophospholipids (lecithins, kephalins, phosphatidyl serine), glyceroglycolipids (galactopyransoide), sphingophospholipids (sphingomyelin), and sphingoglycolipids (ceramides, gangliosides), DSS (docusate sodium, CAS registry no [577-11-7]), docusate calcium, CAS registry no [128-49-4]), docusate potassium, CAS registry no [7491-09-0]), SDS (sodium dodecyl sulfate or sodium lauryl sulfate), dipalmitoyl phosphatidic acid, sodium caprylate,
- N-alkyl-N,N-dimethylammonio-1-propanesulfonates 3-cholamido-1-propyldimethylammonio-1-propanesulfonate
- dodecylphosphocholine myristoyl lysophosphatidylcholine
- hen egg lysolecithin cationic surfactants (quarternary ammonium bases) (e.g.
- acylcarnitines and derivatives N ⁇ -acylated derivatives of lysine, arginine or histidine, or side-chain acylated derivatives of lysine or arginine, N ⁇ -acylated derivatives of dipeptides comprising any combination of lysine, arginine or histidine and a neutral or acidic amino acid, N ⁇ -acylated derivative of a tripeptide comprising any combination of a neutral amino acid and two charged amino acids, or the surfactant may be selected from the group of imidazoline derivatives, or mixtures thereof. Each one of these specific surfactants constitutes an alternative embodiment of the invention.
- the GLP-1 compound is selected from GLP-1(7-36) or an analogue thereof having a lysine residue wherein a lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from a GLP-1(7-36) analogue having one lysine residue wherein one lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from Arg26,34,Lys36GLP-1(7-36) having one lysine residue wherein one lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from GLP-1(7-37) or an analogue thereof having a lysine residue wherein a lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from a GLP-1(7-37) analogue having one lysine residue wherein one lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from Arg34GLP-1(7-37), or Arg26GLP-1(7-37) having one lysine residue wherein one lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from GLP-1(7-38) or an analogue thereof having a lysine residue wherein a lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from a GLP-1(7-38) analogue having one lysine residue wherein one lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from Gly8,Arg26,34,Glu37,Lys38GLP-1(7-38) having one lysine residue wherein one lipophilic substituent optionally via a spacer is attached to the epsilon amino group of said lysine.
- the GLP-1 compound is selected from GLP-1(7-37) or an analogue thereof having one lipophilic substituent optionally attached via a spacer.
- the lipophilic substituent is attached to any one of the amino acid residues in position 18-37, typically 26-34.
- the lipophilic substituent is attached to any one of the amino acid residues in position 18-36, typically 26-34.
- the lipophilic substituent is attached to any one of the amino acid residues in position 18-38, typically 26-34.
- an analogue is used to designate a peptide wherein one or more amino acid residues of the parent peptide have been substituted by another amino acid residue and/or wherein one or more amino acid residues of the parent peptide have been deleted and/or wherein one or more amino acid residues have been added to the parent peptide. Such addition can take place either at the N-terminal end or at the C-terminal end of the parent peptide or both.
- GLP-1(7-37) or an analogue thereof comprises GLP-1(7-36), GLP-1(7-37), and GLP-1(7-38), and analogues thereof wherein at least one, preferably at least 3, more preferable at least 5 amino acid residues have been substituted by another amino acid residue.
- the GLP-1 compound binds to a GLP-1 receptor, preferably with an affinity constant (K D ) or a potency (EC 50 ) of below 1 ⁇ M, e.g. below 100 nM (measured as known in the art, see e.g. WO 98/08871).
- GLP-1 compound encompasses GLP-1(7-37) and analogues thereof as well as derivatives of any of the foregoing.
- Derivatives of GLP-1 analogues are GLP-1 analogues which are chemically modified by introducing e.g. ester, alkyl or lipophilic functionalities on one or more amino acid residues of GLP-1 analogues. Methods for identifying GLP-1 compounds are described in WO 93/19175 (Novo Nordisk A/S).
- lipophilic substituent is characterised by comprising 4-40 carbon atoms and having a solubility in water at 20° C. in the range from about 0.1 mg/100 ml water to about 250 mg/100 ml water, such as in the range from about 0.3 mg/100 ml water to about 75 mg/100 ml water.
- octanoic acid (C8) has a solubility in water at 20° C. of 68 mg/100 ml
- decanoic acid (C10) has a solubility in water at 20° C. of 15 mg/100 ml
- octadecanoic acid (C18) has a solubility in water at 20° C. of 0.3 mg/100 ml.
- the lipophilic substituent may be attached to an amino group of the GLP-1(7-37) or an analogue thereof by means of a carboxyl group of the lipophilic substituent which forms an amide bond with an amino group of the amino acid residue to which it is attached.
- the lipophilic substituent may be attached to said amino acid residue in such a way that an amino group of the lipophilic substituent forms an amide bond with a carboxyl group of the amino acid residue.
- the lipophilic substituent may be linked to the GLP-1(7-37) or an analogue thereof via an ester bond.
- the ester can be formed either by reaction between a carboxyl group of the GLP-1(7-37) or an analogue thereof and a hydroxyl group of the substituent-to-be or by reaction between a hydroxyl group of the GLP-1(7-37) or an analogue thereof and a carboxyl group of the substituent-to-be.
- the lipophilic substituent can be an alkyl group which is introduced into a primary amino group of the GLP-1(7-37) or an analogue thereof.
- the lipophilic substituent may be attached to the GLP-1(7-37) or an analogue thereof by means of a spacer in such a way that a carboxyl group of the spacer forms an amide bond with an amino group of the GLP-1(7-37) or an analogue thereof.
- a spacer must contain at least two functional groups, one to attach to a functional group of the lipophilic substituent and the other to a functional group of the parent GLP-1(7-37) or an analogue thereof.
- spacer is used in the present text to designate a bivalent moiety which contain at least two functional groups, one to attach to a functional group of the lipophilic substituent and the other to a functional group of the GLP-1 compound.
- suitable spacers are succinic acid, lysyl, glutamyl, asparagyl, glycyl, beta-alanyl and gamma-aminobutanoyl, or a dipeptide such as Gly-Lys, each of which constitutes an individual embodiment.
- one carboxyl group thereof may form an amide bond with an amino group of the amino acid residue, and the other carboxyl group thereof may form an amide bond with an amino group of the lipophilic substituent.
- the spacer is lysyl, glutamyl, asparagyl, glycyl, beta-alanyl or gamma-aminobutanoyl
- the carboxyl group thereof may form an amide bond with an amino group of the amino acid residue
- the amino group thereof may form an amide bond with a carboxyl group of the lipophilic substituent.
- a further spacer may in some instances be inserted between the ⁇ -amino group of Lys and the lipophilic substituent.
- a further spacer is succinic acid which forms an amide bond with the ⁇ -amino group of Lys and with an amino group present in the lipophilic substituent.
- such a further spacer is Glu or Asp which forms an amide bond with the ⁇ -amino group of Lys and another amide bond with a carboxyl group present in the lipophilic substituent, that is, the lipophilic substituent is a N ⁇ -acylated lysine residue.
- the spacer is an amino acid residue except Cys or Met, or a dipeptide such as Gly-Lys.
- a dipeptide such as Gly-Lys means any combination of two amino acids except Cys or Met, typically a dipeptide wherein the C-terminal amino acid residue is Lys, His or Trp, typically Lys, and the N-terminal amino acid residue is Ala, Arg, Asp, Asn, Gly, Glu, Gln, lle, Leu, Val, Phe, Pro, Ser, Tyr, Thr, Lys, His and Trp.
- an amino group of the GLP-1 compound forms an amide bond with a carboxylic group of the amino acid residue or dipeptide spacer
- an amino group of the amino acid residue or dipeptide spacer forms an amide bond with a carboxyl group of the lipophilic substituent
- the lipophilic substituent has from 8 to 40 carbon atoms. In a further embodiment of the invention the lipophilic substituent has from 10 to 24 carbon atoms. In a further embodiment of the invention the lipophilic substituent has from 12 to 24 carbon atoms. In a further embodiment of the invention the lipophilic substituent has from 12 to 18 carbon atoms. In a further embodiment of the invention the lipophilic substituent has from 14 to 18 carbon atoms.
- the spacer is present. In a further embodiment of the invention the spacer is selected from an amino acid. In a further embodiment of the invention, the spacer is an amino acid residue except Cys or Met. In another embodiment, the spacer is a dipeptide such as Gly-Lys. In a further embodiment the spacer is selected from lysyl, glutamyl, asparagyl, glycyl, beta-alanyl and gamma-aminobutanoyl, each of which constitutes an individual embodiment. Typically used spacers are glutamyl, aminobutyroyl, and beta-alanyl (beta-Ala).
- the spacer is an unbranched alkane ⁇ , ⁇ -dicarboxylic acid group having from 1 to 7 methylene groups, which spacer forms a bridge between an amino group of the parent peptide and an amino group of the lipophilic substituent.
- the spacer is succinic acid.
- the lipophilic substituent(s) contain a functional group which can be attached to one of the following functional groups of an amino acid of the parent GLP-1(7-37) or an analogue thereof:
- the lipophilic substituent is attached to the carboxy group of the R group of any Asp and Glu residue.
- a lipophilic substituent is attached to the carboxy group attached to the alpha-carbon of the C-terminal amino acid.
- a lipophilic substituent is attached to the epsilon-amino group of any Lys residue.
- Each lipophilic substituent contains a functional group which may be attached to a functional group of an amino acid of the parent GLP-1(7-37) or an analogue thereof.
- a lipophilic substituent may contain a carboxyl group which can be attached to an amino group of the parent GLP-1(7-37) or an analogue thereof by means of an amide bond.
- the lipophilic substituent comprises a partially or completely hydrogenated cyclopentanophenathrene skeleton.
- the lipophilic substituent is a straight chain or branched alkyl group.
- the lipophilic substituent is an acyl group of a straight-chain or branched fatty acid.
- the lipophilic substituent is an acyl group having the formula CH 3 (CH 2 ) n CO—, wherein n is an integer from 4 to 38. In a further embodiment n is an integer from 12 to 38. In further embodiments the lipophilic substituent is selected from the following individual embodiments CH 3 (CH 2 ) 12 CO—, CH 3 (CH 2 ) 14 CO—, CH 3 (CH 2 ) 16 CO—, CH 3 (CH 2 ) 18 CO—, CH 3 (CH 2 ) 20 CO— and CH 3 (CH 2 ) 22 CO—. In a specific embodiment, the lipophilic substituent is tetradecanoyl. In another specific embodiment, the lipophilic substituent is hexadecanoyl.
- the lipophilic substituent has a group which is negatively charged such as a carboxylic acid group.
- the lipophilic substituent may be an acyl group of a straight-chain or branched alkane ⁇ , ⁇ -dicarboxylic acid of the formula HOOC(CH 2 ) m CO—, wherein m is an integer from 4 to 38, preferably an integer from 12 to 38, and most preferably is HOOC(CH 2 ) 14 CO—, HOOC(CH 2 ) 16 CO—, HOOC(CH 2 ) 18 CO—, HOOC(CH 2 ) 20 CO— or HOOC(CH 2 ) 22 CO—.
- the GLP-1 compound is Arg 26 , 34 ,Lys 36 -(N-epsilon-(gamma-L-glutamyl(N-alfa-hexadecanoyl)))-GLP-1(7-36).
- the GLP-1 compound is Arg 26 ,Lys 34 -(N-epsilon-(gamma-L-glutamyl(N-alfa-hexadecanoyl)))-GLP-1(7-37).
- the GLP-1 compound is Gly 8 ,Arg 26,34 , Glu 37 , Lys 38 -(N-epsilon-(gamma-L-glutamyl(N-alfa-hexadecanoyl)))-GLP-1(7-38).
- the GLP-1 compound is Arg 34 ,Lys 26 -(N-epsilon-(gamma-aminobutyroyl(N-gamma-hexadecanoyl)))-GLP-1(7-37).
- the GLP-1 compound is Arg 34 ,Lys 26 -(N-epsilon-(beta-alanyl(N-beta-hexadecanoyl)))-GLP-1(7-37).
- the GLP-1 compound is Arg 34 ,Lys 26 -(N-epsilon-(beta-alanyl-(N-beta-tetradecanoyl)))-GLP-1(7-37).
- the GLP-1 compound is Arg 34 ,Lys 26 -(N-epsilon-(gamma-aminobutyroyl)-(N-gamma-tetradecanoyl))-GLP-1-(7-37).
- the GLP-1 compound is Arg 34 ,Lys 26 -(N-epsilon-(beta-alanyl-(N-beta-16-hydroxyhexadecanoyl)))-GLP-1(7-37).
- the GLP-1 compound is Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37).
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 7 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 7 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.9
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 7 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 7 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.1.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycylglycine, 16.0 mg/ml glycerol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycylglycine, 16.0 mg/ml glycerol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1 (7-37), glycylglycine, 16.0 mg/ml glycerol, and 5 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycylglycine, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycylglycine, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycylglycine, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 7.9.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 38.5 mg/ml mannitol, and either 3 mg/ml mcresol or 1.5 mg/ml phenol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 38.5 mg/ml mannitol, and either 3 mg/ml mcresol or 1.5 mg/ml phenol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 38.5 mg/ml mannitol, and either 3 mg/ml mcresol or 1.5 mg/ml phenol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 38.5 mg/ml mannitol, and either 3 mg/ml mcresol or 1.5 mg/ml phenol, at pH 7.0.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.8.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.8.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.8.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate/sodium dihydrogen phosphate, 17.0 mg/ml mannitol, and 18 mg/ml benzylalcohol, at pH 7.8.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and either 1 mg/ml EDTA or 1.55 mg/ml L-His, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1 mg/ml EDTA/1.55 mg/ml L-His, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, 7 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, 7 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, 7 mg/ml phenol, and 1.55 mg/ml L-His, at pH 7.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and either 1 mg/ml EDTA or 1.55 mg/ml L-His, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and either 1 mg/ml EDTA or 1 .55 mg/ml L-His, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and either 4 mg/ml Poloxamer 188 or 30 mg/ml PEG 35000, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and either 4 mg/ml Poloxamer 188 or 30 mg/ml PEG 35000, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and either 4 mg/ml Poloxamer 188 or 30 mg/ml PEG 35000, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), glycine, 36.9 mg/ml mannitol, 5 mg/ml phenol, and either 4 mg/ml Poloxamer 188 or 30 mg/ml PEG 35000, at pH 9.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 7 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 16.0 mg/ml glycerol, and 7 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1 (7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 7 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, and 5 mg/ml phenol, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 1 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 2 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 3 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 5 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.4.
- the invention relates to a pharmaceutical formulation consisting of an aqueous solution of 7 mg/ml Arg 34 , Lys 26 (N- ⁇ -( ⁇ -Glu(N- ⁇ -hexadecanoyl)))-GLP-1(7-37), disodium hydrogen phosphate, 36.9 mg/ml mannitol, 5 mg/ml phenol, and 1.55 mg/ml L-His, at pH 8.4.
- the parent peptide, GLP-1(7-37) or analogue thereof can be produced by a method which comprises culturing a host cell containing a DNA sequence encoding the polypeptide and capable of expressing the polypeptide in a suitable nutrient medium under conditions permitting the expression of the peptide, after which the resulting peptide is recovered from the culture.
- the medium used to culture the cells may be any conventional medium suitable for growing the host cells, such as minimal or complex media containing appropriate supplements. Suitable media are available from commercial suppliers or may be prepared according to published recipes (e.g. in catalogues of the American Type Culture Collection).
- the peptide produced by the cells may then be recovered from the culture medium by conventional procedures including separating the host cells from the medium by centrifugation or filtration, precipitating the proteinaceous components of the supernatant or filtrate by means of a salt, e.g. ammonium sulphate, purification by a variety of chromatographic procedures, e.g. ion exchange chromatography, gel filtration chromatography, affinity chromatography, or the like, dependent on the type of peptide in question.
- a salt e.g. ammonium sulphate
- the DNA sequence encoding the parent peptide may suitably be of genomic or cDNA origin, for instance obtained by preparing a genomic or cDNA library and screening for DNA sequences coding for all or part of the peptide by hybridisation using synthetic oligonucleotide probes in accordance with standard techniques (see, for example, Sambrook, J, Fritsch, EF and Maniatis, T, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, New York, 1989).
- the DNA sequence encoding the peptide may also be prepared synthetically by established standard methods, e.g.
- the DNA sequence may also be prepared by polymerase chain reaction using specific primers, for instance as described in U.S. Pat. No. 4,683,202 or Saiki et al., Science 239 (1988), 487-491.
- the DNA sequence may be inserted into any vector which may conveniently be subjected to recombinant DNA procedures, and the choice of vector will often depend on the host cell into which it is to be introduced.
- the vector may be an autonomously replicating vector, i.e. a vector which exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g. a plasmid.
- the vector may be one which, when introduced into a host cell, is integrated into the host cell genome and replicated together with the chromosome(s) into which it has been integrated.
- the vector is preferably an expression vector in which the DNA sequence encoding the peptide is operably linked to additional segments required for transcription of the DNA, such as a promoter.
- the promoter may be any DNA sequence which shows transcriptional activity in the host cell of choice and may be derived from genes encoding proteins either homologous or heterologous to the host cell. Examples of suitable promoters for directing the transcription of the DNA encoding the peptide of the invention in a variety of host cells are well known in the art, cf. for instance Sambrook et al., supra.
- the DNA sequence encoding the peptide may also, if necessary, be operably connected to a suitable terminator, polyadenylation signals, transcriptional enhancer sequences, and translational enhancer sequences.
- the recombinant vector of the invention may further comprise a DNA sequence enabling the vector to replicate in the host cell in question.
- the vector may also comprise a selectable marker, e.g. a gene the product of which complements a defect in the host cell or one which confers resistance to a drug, e.g. ampicillin, kanamycin, tetracyclin, chloramphenicol, neomycin, hygromycin or methotrexate.
- a selectable marker e.g. a gene the product of which complements a defect in the host cell or one which confers resistance to a drug, e.g. ampicillin, kanamycin, tetracyclin, chloramphenicol, neomycin, hygromycin or methotrexate.
- a secretory signal sequence (also known as a leader sequence, prepro sequence or pre sequence) may be provided in the recombinant vector.
- the secretory signal sequence is joined to the DNA sequence encoding the peptide in the correct reading frame.
- Secretory signal sequences are commonly positioned 5′ to the DNA sequence encoding the peptide.
- the secretory signal sequence may be that normally associated with the peptide or may be from a gene encoding another secreted protein.
- the host cell into which the DNA sequence or the recombinant vector is introduced may be any cell which is capable of producing the present peptide and includes bacteria, yeast, fungi and higher eukaryotic cells.
- suitable host cells well known and used in the art are, without limitation, E. coli, Saccharomyces cerevisiae , or mammalian BHK or CHO cell lines.
- Compound 1 is intended to mean: Arg 34 , Lys 26 (N ⁇ -( ⁇ -Glu(N ⁇ -hexadecanoyl))) GLP-1(7-37).
- the turbidity of the formulation is characterized by a visual score ranking the degree of turbidity from 0 to 3 (a formulation showing no turbidity corresponds to a visual score 0, and a formulation showing visual turbidity in daylight corresponds to visual score 3).
- a formulation is classified physical unstable with respect to protein aggregation, when it shows visual turbidity in daylight.
- the turbidity is also measured in Nephelometric Turbidity Units (NTU) with a nephelometer, which has been calibrated with a Formazin standard.
- NTU Nephelometric Turbidity Units
- a formulation with a turbidity>>10 NTU is regarded as physical unstable.
- Preservative, isotonic agent and buffer were dissolved and pH was adjusted to the specified pH.
- the Compound 1 or GLP1(7-37) was dissolved under slow stirring.
- the pH was adjusted to the specified using Sodium Hydroxide and/or Hydrochloric Acid.
- the formulation was sterilised by filtration through a 0.22 ⁇ m sterile filter. Visual inspection at Turbidity Isotonic 5° C. (visual measurements Compound Amount pH Buffer agent Preservative score) at 5° C.
- Buffer was dissolved and pH was adjusted to the specified pH.
- the Compound 1 was dissolved under slow stirring.
- the pH was adjusted to the specified using Sodium Hydroxide and/or Hydrochloric Acid.
- the formulation was sterilised by filtration through a 0.22 ⁇ m sterile filter.
- Preservative and buffer was dissolved and pH was adjusted to the specified pH.
- the Compound 1 was dissolved under slow stirring.
- the pH was adjusted to the specified using Sodium Hydroxide and/or Hydrochloric Acid.
- the formulation was sterilised by filtration through a 0.22 ⁇ m sterile filter.
- Preservative, isotonic agent and buffer were dissolved and pH was adjusted to the specified pH.
- the Compound 1 was dissolved under slow stirring.
- the pH was adjusted to the specified using Sodium Hydroxide and/or Hydrochloric Acid.
- the formulation was sterilised by filtration through a 0.22 ⁇ m sterile filter.
- Preservative, isotonic agent, buffer, and further additive(s) selected from chelating agent, stabiliser and surfactant were dissolved and pH was adjusted to the specified pH.
- the Compound 1 was dissolved under slow stirring.
- the pH was adjusted to the specified using Sodium Hydroxide and/or Hydrochloric Acid.
- the formulation was sterilised by filtration through a 0.22 ⁇ m sterile filter.
- Preservative, isotonic agent and buffer were dissolved and pH adjusted to the specified pH.
- the Compound was dissolved under slow stirring.
- the pH was adjusted to the specified using Sodium Hydroxide and/or Hydrochloric Acid.
- the formulation was sterilised by filtration through a 0.22 ⁇ m sterile filter. The physical stability was followed at 5, 25 and 37° C.
- the physical stability is evaluated by visual inspection and Turbidity measurements in NTU as described in Example 1.
- Visual Turbidity Amount of Isotonic inspection measurements Compound 1 PH Buffer agent Preservative Temp. (visual score) (NTU) 3 mg/ml 8.4 Disodium Glycerol Phenol 5° C. 0.5 1.0 hydrogen 16.0 mg/ml 7 mg/ml (12 weeks) (6 weeks) phosphate 3 mg/ml 8.4 Disodium Glycerol Phenol 5° C. 1 0.6 hydrogen 16.0 mg/ml 7 mg/ml (15 months) (15 months) phosphate 3 mg/ml 8.4 Disodium Glycerol Phenol 25° C.
- the formulation is physically stable after storage at 5° C. for more than 15 months and after storage at, 25 and 37° C. it is physically stable for more than 12 weeks.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/185,923 US20030119734A1 (en) | 2001-06-28 | 2002-06-27 | Stable formulation of modified GLP-1 |
US11/786,095 US20080167226A1 (en) | 2001-06-28 | 2007-04-11 | Stable formulation of modified GLP-1 |
US12/343,722 US20090111752A1 (en) | 2001-06-28 | 2008-12-24 | Stable Formulation of Modified GLP-1 |
US12/785,861 US8846618B2 (en) | 2001-06-28 | 2010-05-24 | Stable formulation of modified GLP-1 |
Applications Claiming Priority (15)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DKPA200101011 | 2001-06-28 | ||
DKPA200101011 | 2001-06-28 | ||
DKPA200101010 | 2001-06-28 | ||
DKPA200101010 | 2001-06-28 | ||
DKPA200101053 | 2001-07-04 | ||
DKPA200101053 | 2001-07-04 | ||
DKPA200101052 | 2001-07-04 | ||
DKPA200101052 | 2001-07-04 | ||
US30832501P | 2001-07-27 | 2001-07-27 | |
US30829701P | 2001-07-27 | 2001-07-27 | |
DKPA200200093 | 2002-01-18 | ||
DKPA200200092 | 2002-01-18 | ||
DKPA200200093 | 2002-01-18 | ||
DKPA200200092 | 2002-01-18 | ||
US10/185,923 US20030119734A1 (en) | 2001-06-28 | 2002-06-27 | Stable formulation of modified GLP-1 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/786,095 Continuation US20080167226A1 (en) | 2001-06-28 | 2007-04-11 | Stable formulation of modified GLP-1 |
US12/343,722 Continuation US20090111752A1 (en) | 2001-06-28 | 2008-12-24 | Stable Formulation of Modified GLP-1 |
Publications (1)
Publication Number | Publication Date |
---|---|
US20030119734A1 true US20030119734A1 (en) | 2003-06-26 |
Family
ID=27545250
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/185,923 Abandoned US20030119734A1 (en) | 2001-06-28 | 2002-06-27 | Stable formulation of modified GLP-1 |
US11/786,095 Abandoned US20080167226A1 (en) | 2001-06-28 | 2007-04-11 | Stable formulation of modified GLP-1 |
US12/343,722 Abandoned US20090111752A1 (en) | 2001-06-28 | 2008-12-24 | Stable Formulation of Modified GLP-1 |
US12/785,861 Expired - Lifetime US8846618B2 (en) | 2001-06-28 | 2010-05-24 | Stable formulation of modified GLP-1 |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/786,095 Abandoned US20080167226A1 (en) | 2001-06-28 | 2007-04-11 | Stable formulation of modified GLP-1 |
US12/343,722 Abandoned US20090111752A1 (en) | 2001-06-28 | 2008-12-24 | Stable Formulation of Modified GLP-1 |
US12/785,861 Expired - Lifetime US8846618B2 (en) | 2001-06-28 | 2010-05-24 | Stable formulation of modified GLP-1 |
Country Status (10)
Country | Link |
---|---|
US (4) | US20030119734A1 (ja) |
EP (1) | EP1412384B1 (ja) |
JP (2) | JP5562510B2 (ja) |
AT (1) | ATE382057T1 (ja) |
AU (1) | AU2002316811A1 (ja) |
DE (1) | DE60224284T2 (ja) |
DK (1) | DK1412384T3 (ja) |
ES (1) | ES2298378T3 (ja) |
PT (1) | PT1412384E (ja) |
WO (1) | WO2003002136A2 (ja) |
Cited By (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040037818A1 (en) * | 1998-07-30 | 2004-02-26 | Brand Stephen J. | Treatment for diabetes |
US20040209816A1 (en) * | 1999-01-29 | 2004-10-21 | Indu Parikh | Treatment for diabetes |
US20040209801A1 (en) * | 2002-10-22 | 2004-10-21 | Brand Stephen J. | Treatment of diabetes |
US20050143303A1 (en) * | 2003-12-26 | 2005-06-30 | Nastech Pharmaceutical Company Inc. | Intranasal administration of glucose-regulating peptides |
US20050260259A1 (en) * | 2004-04-23 | 2005-11-24 | Bolotin Elijah M | Compositions for treatment with glucagon-like peptide, and methods of making and using the same |
US20060074025A1 (en) * | 2003-12-26 | 2006-04-06 | Nastech Pharmaceutical Company Inc. | Therapeutic formulations for transmucosal administration that increase glucagon-like peptide-1 bioavailability |
US20060211616A1 (en) * | 2003-08-21 | 2006-09-21 | Novo Nordisk A/S | Purification of glucagon-like peptides |
US20060234373A1 (en) * | 2002-05-24 | 2006-10-19 | Alex Rabinovitch | Treatment for diabetes |
US20060239924A1 (en) * | 2002-02-27 | 2006-10-26 | Bolotin Elijah M | Compositions for delivery of therapeutics and other materials, and methods of making and using the same |
US20060247167A1 (en) * | 2003-09-01 | 2006-11-02 | Novo Nordisk A/S | Stable formulations of peptides |
US20070010424A1 (en) * | 2003-11-20 | 2007-01-11 | Novo Nordisk A/S | Propylene glycol-containing peptide formulations which are optimal for production and for use in injection devices |
US20080015263A1 (en) * | 2002-02-27 | 2008-01-17 | Bolotin Elijah M | Compositions for delivery of therapeutics and other materials |
US20080171848A1 (en) * | 2004-08-31 | 2008-07-17 | Novo Nordisk A/S | Use of Tris(Hydroxymethyl) Aminomethane For the Stabilization of Peptides, Polypeptides and Proteins |
US20080234200A1 (en) * | 2003-12-26 | 2008-09-25 | Nastech Pharmaceutical Company Inc. | Method of treatment of a metabolic disease using intranasal administration of exendin peptide |
US20080318865A1 (en) * | 2003-06-03 | 2008-12-25 | Novo Nordisk A/S | Stabilized Pharmaceutical Peptide Compositions |
US20080318837A1 (en) * | 2003-12-26 | 2008-12-25 | Nastech Pharmaceutical Company Inc. | Pharmaceutical Formation For Increased Epithelial Permeability of Glucose-Regulating Peptide |
US20080318861A1 (en) * | 2005-12-08 | 2008-12-25 | Nastech Pharmaceutical Company Inc. | Mucosal Delivery of Stabilized Formulations of Exendin |
US20090053169A1 (en) * | 2007-08-20 | 2009-02-26 | Pharmain Corporation | Oligonucleotide Core Carrier Compositions for Delivery of Nucleic Acid-Containing Therapeutic Agents, Methods of Making and Using the Same |
US20090088387A1 (en) * | 2007-08-03 | 2009-04-02 | Pharmain Corporation | Composition for long-acting peptide analogs |
US20090176892A1 (en) * | 2008-01-09 | 2009-07-09 | Pharmain Corporation | Soluble Hydrophobic Core Carrier Compositions for Delivery of Therapeutic Agents, Methods of Making and Using the Same |
US7560425B2 (en) | 2002-06-07 | 2009-07-14 | Waratah Pharmaceuticals Inc. | Pharmaceutical composition consisting of rapamycine and gastrin 17(LEU15) and a method for treating diabetes |
US20090202494A1 (en) * | 2004-01-30 | 2009-08-13 | Antonio Cruz | Combined use of glp-1 agonists and gastrin for regulating blood glucose levels |
US20100056451A1 (en) * | 2003-06-03 | 2010-03-04 | Novo Nordisk A/S | Stabilized Pharmaceutical Peptide Compositions |
US20100173844A1 (en) * | 2004-11-12 | 2010-07-08 | Novo Nordisk A/S | Stable Formulations of Peptides |
US20100234299A1 (en) * | 2001-06-28 | 2010-09-16 | Novo Nordisk A/S | Stable formulation of modified glp-1 |
WO2011123943A1 (en) | 2010-04-09 | 2011-10-13 | Mount Sinai Hospital | Methods for treating disorders of the gastrointestinal tract using a glp-1 agonist |
US9670261B2 (en) | 2012-12-21 | 2017-06-06 | Sanofi | Functionalized exendin-4 derivatives |
US9694053B2 (en) | 2013-12-13 | 2017-07-04 | Sanofi | Dual GLP-1/glucagon receptor agonists |
US9737615B2 (en) | 2005-12-19 | 2017-08-22 | PharmalN Corporation | Hydrophobic core carrier compositions for delivery of therapeutic agents, methods of making and using the same |
US9750788B2 (en) | 2013-12-13 | 2017-09-05 | Sanofi | Non-acylated exendin-4 peptide analogues |
US9751926B2 (en) | 2013-12-13 | 2017-09-05 | Sanofi | Dual GLP-1/GIP receptor agonists |
US9758561B2 (en) | 2014-04-07 | 2017-09-12 | Sanofi | Dual GLP-1/glucagon receptor agonists derived from exendin-4 |
US9771406B2 (en) | 2014-04-07 | 2017-09-26 | Sanofi | Peptidic dual GLP-1/glucagon receptor agonists derived from exendin-4 |
US9775904B2 (en) | 2014-04-07 | 2017-10-03 | Sanofi | Exendin-4 derivatives as peptidic dual GLP-1/glucagon receptor agonists |
US9789165B2 (en) | 2013-12-13 | 2017-10-17 | Sanofi | Exendin-4 peptide analogues as dual GLP-1/GIP receptor agonists |
US9932381B2 (en) | 2014-06-18 | 2018-04-03 | Sanofi | Exendin-4 derivatives as selective glucagon receptor agonists |
US9982029B2 (en) | 2015-07-10 | 2018-05-29 | Sanofi | Exendin-4 derivatives as selective peptidic dual GLP-1/glucagon receptor agonists |
US10758592B2 (en) | 2012-10-09 | 2020-09-01 | Sanofi | Exendin-4 derivatives as dual GLP1/glucagon agonists |
US10806797B2 (en) | 2015-06-05 | 2020-10-20 | Sanofi | Prodrugs comprising an GLP-1/glucagon dual agonist linker hyaluronic acid conjugate |
CN112912100A (zh) * | 2018-10-26 | 2021-06-04 | 诺和诺德股份有限公司 | 稳定的司美鲁肽组合物及其用途 |
US11318191B2 (en) | 2020-02-18 | 2022-05-03 | Novo Nordisk A/S | GLP-1 compositions and uses thereof |
US11752198B2 (en) | 2017-08-24 | 2023-09-12 | Novo Nordisk A/S | GLP-1 compositions and uses thereof |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2545090T3 (es) | 2001-12-21 | 2015-09-08 | Human Genome Sciences, Inc. | Proteínas de fusión de albúmina y GCSF |
BR0306685A (pt) | 2002-05-21 | 2005-04-26 | Daiichi Suntory Pharma Co Ltd | Composição farmacêutica contendo grelina |
KR101198346B1 (ko) | 2003-04-08 | 2012-11-06 | 노보 노르디스크 에이/에스 | 크로마토그래피 고정상의 재생 |
WO2004089985A1 (en) * | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | Stable pharmaceutical compositions |
CN102174102A (zh) | 2003-05-15 | 2011-09-07 | 塔夫茨大学信托人 | 肽和多肽药物的稳定类似物 |
PL1633390T3 (pl) * | 2003-06-03 | 2012-06-29 | Novo Nordisk As | Stabilizowane kompozycje farmaceutyczne peptydu glp-1 |
CA2531988C (en) | 2003-08-05 | 2016-06-28 | Novo Nordisk A/S | Novel insulin derivatives |
EP1663295A2 (en) * | 2003-09-01 | 2006-06-07 | Novo Nordisk A/S | Stable formulations of peptides |
WO2005023291A2 (en) * | 2003-09-11 | 2005-03-17 | Novo Nordisk A/S | Use of glp1-agonists in the treatment of patients with type i diabetes |
EP1667724A2 (en) * | 2003-09-19 | 2006-06-14 | Novo Nordisk A/S | Albumin-binding derivatives of therapeutic peptides |
CA2539253A1 (en) | 2003-09-19 | 2005-03-31 | Novo Nordisk A/S | Albumin-binding derivatives of therapeutic peptides |
JP4865565B2 (ja) | 2003-12-09 | 2012-02-01 | ノヴォ ノルディスク アー/エス | Glp−1アゴニストを用いた食物選択の制御 |
TWI353250B (en) * | 2003-12-16 | 2011-12-01 | Ipsen Pharma Sas | Glp-1 pharmaceutical compositions |
EP1758575A1 (en) | 2004-06-11 | 2007-03-07 | Novo Nordisk A/S | Counteracting drug-induced obesity using glp-1 agonists |
CN101022822B (zh) * | 2004-08-24 | 2012-06-27 | 第一三共株式会社 | 生理学活性肽的液体制剂 |
WO2006037811A2 (en) | 2004-10-07 | 2006-04-13 | Novo Nordisk A/S | Protracted exendin-4 compounds |
JP2008515856A (ja) * | 2004-10-07 | 2008-05-15 | ノボ ノルディスク アクティーゼルスカブ | 遅延性glp−1化合物 |
NZ555464A (en) | 2004-12-02 | 2010-03-26 | Domantis Ltd | Bispecific domain antibodies targeting serum albumin and glp-1 or pyy |
US8871712B2 (en) | 2005-01-14 | 2014-10-28 | Camurus Ab | Somatostatin analogue formulations |
SI1845942T1 (sl) | 2005-01-14 | 2014-06-30 | Camurus Ab | Gnrh analogne formulacije |
US9649382B2 (en) | 2005-01-14 | 2017-05-16 | Camurus Ab | Topical bioadhesive formulations |
KR101245022B1 (ko) | 2005-01-21 | 2013-03-19 | 카무러스 에이비 | 약제학적 지질 조성물 |
TWI362392B (en) | 2005-03-18 | 2012-04-21 | Novo Nordisk As | Acylated glp-1 compounds |
KR20070120112A (ko) | 2005-03-18 | 2007-12-21 | 노보 노르디스크 에이/에스 | 연장형 glp-1 화합물 |
US20090227493A1 (en) * | 2005-05-27 | 2009-09-10 | Daiichi Sankyo Company, Limited | Combined drug for treating diabetes |
US8546326B2 (en) | 2005-06-06 | 2013-10-01 | Camurus Ab | Glp-1 analogue formulations |
DE602005017628D1 (de) | 2005-09-22 | 2009-12-24 | Biocompatibles Uk Ltd | Fusionspolypeptide vom glp-1 (glucagon-like peptide-1) mit erhöhten peptidaseresistenz |
PT1969004E (pt) | 2005-12-28 | 2011-11-25 | Novo Nordisk As | Composições que compreendem uma insulina acilada e zinco e método para criar tais composições |
DE602006009631D1 (de) * | 2006-05-10 | 2009-11-19 | Biocompatibles Uk Ltd | GLP-1 Peptide enthaltende kugelförmige Mikrokapseln, deren Produktion und deren Verwendung |
US9034818B2 (en) | 2007-06-13 | 2015-05-19 | Novo Nordisk A/S | Pharmaceutical formulations comprising an insulin derivative |
GB0711656D0 (en) | 2007-06-15 | 2007-07-25 | Camurus Ab | Formulations |
GB0716385D0 (en) | 2007-08-22 | 2007-10-03 | Camurus Ab | Formulations |
EA018471B1 (ru) | 2008-03-31 | 2013-08-30 | Глаксо Груп Лимитед | Слитые конструкции и конъюгаты лекарственного средства |
KR20110039348A (ko) | 2008-08-06 | 2011-04-15 | 노보 노르디스크 헬스 케어 악티엔게젤샤프트 | 연장된 생체내 효능을 가지는 콘쥬게이트된 단백질 |
GB0815435D0 (en) | 2008-08-22 | 2008-10-01 | Camurus Ab | Formulations |
EP2163243A1 (en) * | 2008-09-12 | 2010-03-17 | Biocompatibles UK Limited | Treatment of acute myocardial infarction (AMI) using encapsulated cells encoding and secreting GLP-1 peptides or analogs thereof |
AU2009309623B9 (en) | 2008-10-30 | 2014-10-02 | Novo Nordisk A/S | Treating diabetes melitus using insulin injections with less than daily injection frequency |
AU2009324037B2 (en) | 2008-12-05 | 2015-07-30 | Glaxo Group Limited | Methods for selecting protease resistant polypeptides |
KR20110122100A (ko) | 2009-01-22 | 2011-11-09 | 노보 노르디스크 헬스 케어 악티엔게젤샤프트 | 안정한 성장 호르몬 화합물 |
BRPI1013588A2 (pt) | 2009-03-27 | 2016-04-19 | Glaxo Group Ltd | composição |
EP2461831B1 (en) | 2009-08-06 | 2018-11-21 | Novo Nordisk Health Care AG | Growth hormones with prolonged in-vivo efficacy |
EA201290123A1 (ru) | 2009-09-30 | 2012-10-30 | Глаксо Груп Лимитед | Продукты слияния и конъюгаты лекарственных средств с увеличенным периодом полувыведения |
CN102834109B (zh) | 2010-01-22 | 2016-01-20 | 诺沃—诺迪斯克保健股份有限公司 | 稳定的生长激素化合物 |
JP5980689B2 (ja) | 2010-01-22 | 2016-08-31 | ノヴォ・ノルディスク・ヘルス・ケア・アーゲー | 安定な成長ホルモン化合物 |
JP6049625B2 (ja) | 2010-10-27 | 2016-12-21 | ノヴォ ノルディスク アー/エス | 様々な注射間隔を用いて施されるインスリン注射を使用する、真性糖尿病の治療 |
WO2012136790A1 (en) | 2011-04-07 | 2012-10-11 | Glaxo Group Limited | Compositions comprising fusion proteins or conjugates with an improved half -life |
WO2012136792A2 (en) | 2011-04-07 | 2012-10-11 | Glaxo Group Limited | Cck compositions |
US20150038417A1 (en) | 2011-12-09 | 2015-02-05 | Novo Nordisk A/S | GLP-1 Agonists |
ES2834318T3 (es) | 2012-05-25 | 2021-06-17 | Camurus Ab | Formulaciones de agonistas de receptores de la somatostatina |
BR112014032938A2 (pt) | 2012-07-01 | 2017-08-01 | Novo Nordisk As | uso de peptídeos de glp-1 de longa ação |
CN103893744B (zh) * | 2012-12-24 | 2017-12-19 | 杭州九源基因工程有限公司 | 一种治疗糖尿病的药物制剂及其制备方法 |
JP6464145B2 (ja) | 2013-04-05 | 2019-02-06 | ノヴォ・ノルディスク・ヘルス・ケア・アーゲー | 成長ホルモン化合物製剤 |
EP2991672A1 (en) | 2013-04-30 | 2016-03-09 | Novo Nordisk A/S | Novel administration regime |
CN103405753B (zh) * | 2013-08-13 | 2016-05-11 | 上海仁会生物制药股份有限公司 | 稳定的促胰岛素分泌肽水针药物组合物 |
WO2015169789A1 (en) * | 2014-05-07 | 2015-11-12 | Novo Nordisk A/S | Treatment of diabetes type 1 using glp-1 and anti-il-21 |
WO2016038521A1 (en) * | 2014-09-08 | 2016-03-17 | Sun Pharmaceutical Industries Limited | Pharmaceutical compositions of liraglutide |
CN104800572A (zh) * | 2015-04-20 | 2015-07-29 | 陈兴田 | 一种治疗伴抑郁焦虑状态的功能性消化不良的中药制剂 |
CN107249620B (zh) * | 2015-05-13 | 2018-06-26 | 杭州九源基因工程有限公司 | 一种包含glp-1类似物的药物制剂及其制备方法 |
EP3424521A4 (en) * | 2016-03-01 | 2019-12-18 | Hybio Pharmaceutical Co., Ltd | PHARMACEUTICAL COMPOSITION AND PRODUCTION METHOD THEREFOR |
WO2018057977A1 (en) | 2016-09-23 | 2018-03-29 | Delpor, Inc. | Stable compositions for incretin mimetic compounds |
CA3076664C (en) | 2017-09-21 | 2023-10-10 | EMULATE, Inc. | Physiology and pathophysiology of human gut: intestine-on-chip |
US10335464B1 (en) | 2018-06-26 | 2019-07-02 | Novo Nordisk A/S | Device for titrating basal insulin |
EP3897570A1 (en) | 2018-12-19 | 2021-10-27 | KRKA, d.d., Novo mesto | Pharmaceutical composition comprising glp-1 analogue |
WO2020208541A1 (en) | 2019-04-08 | 2020-10-15 | Enzene Biosciences Limited | Composition comprising glp-1 analogue |
US20220372072A1 (en) * | 2019-09-19 | 2022-11-24 | Dr. Reddy's Laboratories Limited | Improved purification processes for liraglutide |
GB201917723D0 (en) | 2019-12-04 | 2020-01-15 | Nv Rose Llc | Stable liquid formulations of glucagon-like peptide 1 or analogues thereof |
WO2021123228A1 (en) | 2019-12-18 | 2021-06-24 | Krka, D.D., Novo Mesto | Pharmaceutical composition comprising glp-1 analogue |
AU2022263996A1 (en) | 2021-04-27 | 2023-11-02 | Aardvark Therapeutics, Inc. | Combination of bitter receptor agonist and gut-signaling compound |
CN113249288B9 (zh) * | 2021-07-13 | 2021-11-09 | 奥锐特药业(天津)有限公司 | 一种表达glp-1类似物的重组菌及其应用 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5652216A (en) * | 1994-05-26 | 1997-07-29 | Novo Nordisk A/S | Pharmaceutical preparation |
US5869602A (en) * | 1995-03-17 | 1999-02-09 | Novo Nordisk A/S | Peptide derivatives |
US6268343B1 (en) * | 1996-08-30 | 2001-07-31 | Novo Nordisk A/S | Derivatives of GLP-1 analogs |
US6380357B2 (en) * | 1997-12-16 | 2002-04-30 | Eli Lilly And Company | Glucagon-like peptide-1 crystals |
US6384016B1 (en) * | 1998-03-13 | 2002-05-07 | Novo Nordisk A/S | Stabilized aqueous peptide solutions |
US20030220255A1 (en) * | 2002-04-04 | 2003-11-27 | Knudsen Liselotte Bjerre | GLP-1 agonist and cardiovascular complications |
Family Cites Families (85)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4483849A (en) * | 1983-01-07 | 1984-11-20 | Carter William A | Stabilization and purification of interferon with propylene glycol, resulting in a non-toxic product |
US4468346A (en) * | 1983-10-27 | 1984-08-28 | The United States Of America As Represented By The Secretary Of Agriculture | Monoclonal antibodies to porcine immunoglobulins |
EP0368864B1 (en) * | 1987-05-14 | 1993-11-03 | Commonwealth Scientific And Industrial Research Organisation | Whey protein fractions |
EP0422124A4 (en) | 1988-06-27 | 1991-10-16 | Genex Corporation | Thermal release of recombinant protein into culture media |
DE69013471T2 (de) | 1989-12-05 | 1995-03-30 | Merck & Co Inc | Methode zur Stabilisierung von rekombinanten Hepatitis-B-Virus-Oberflächenproteinen aus Hefe. |
DE4002066A1 (de) | 1990-01-25 | 1991-08-01 | Basf Ag | Verfahren zur abtrennung von riboflavin aus fermentationssuspensionen |
US5272135A (en) * | 1991-03-01 | 1993-12-21 | Chiron Ophthalmics, Inc. | Method for the stabilization of methionine-containing polypeptides |
SE9101381D0 (sv) | 1991-05-07 | 1991-05-07 | Tomas Moks | Peptide hormone solution |
US5206219A (en) * | 1991-11-25 | 1993-04-27 | Applied Analytical Industries, Inc. | Oral compositions of proteinaceous medicaments |
DK36492D0 (da) | 1992-03-19 | 1992-03-19 | Novo Nordisk As | Praeparat |
DE69307505T2 (de) | 1992-05-13 | 1997-07-24 | Sandoz Ag | Opthalmische zusammensetzungen enthaltend ein cyclosporin |
US6284727B1 (en) * | 1993-04-07 | 2001-09-04 | Scios, Inc. | Prolonged delivery of peptides |
WO1995005848A1 (en) | 1993-08-24 | 1995-03-02 | Novo Nordisk A/S | Protracted glp-1 |
GB9320782D0 (en) * | 1993-10-08 | 1993-12-01 | Univ Leeds Innovations Ltd | Stabilising of proteins on solution |
DK0729362T3 (da) | 1993-11-19 | 2000-05-08 | Searle & Co | Transdermal sammensætning af N-(N-(5-(4-aminoiminomethyl)-phenyl)-1-oxypentyl)-L-alfa-aspartyl)-L-phenylalanin eller estere |
US5705483A (en) * | 1993-12-09 | 1998-01-06 | Eli Lilly And Company | Glucagon-like insulinotropic peptides, compositions and methods |
WO1995022560A1 (en) | 1994-02-22 | 1995-08-24 | The Syntex-Synergen Neuroscience Joint Venture | Pharmaceutical formulations of cntf |
DE69532492T2 (de) | 1994-08-31 | 2004-12-02 | Mitsubishi Pharma Corp. | Verfahren zur Reinigung von rekombinantem menschlichem Serumalbumin |
US5512549A (en) * | 1994-10-18 | 1996-04-30 | Eli Lilly And Company | Glucagon-like insulinotropic peptide analogs, compositions, and methods of use |
WO1996020005A1 (en) * | 1994-12-23 | 1996-07-04 | Novo Nordisk A/S | Protracted glp-1 compositions |
ATE216590T1 (de) | 1995-02-06 | 2002-05-15 | Genetics Inst | Arzneimittelformulierungen für il-12 |
US5834428A (en) * | 1995-04-14 | 1998-11-10 | 1149336 Ontario Inc. | Glucagon-like peptide-2 and its therapeutic use |
US6184201B1 (en) * | 1995-04-14 | 2001-02-06 | Nps Allelix Corp. | Intestinotrophic glucagon-like peptide-2 analogs |
AU5996996A (en) | 1995-06-02 | 1996-12-18 | Novo Nordisk A/S | Al/fe-treatment of a protein solution, followed by membrane concentration |
US5631347A (en) | 1995-06-07 | 1997-05-20 | Eli Lilly And Company | Reducing gelation of a fatty acid-acylated protein |
IL127769A (en) | 1996-07-03 | 2006-10-31 | Alza Corp | Non-aqueous protic preparations of peptides |
JPH10101696A (ja) | 1996-08-08 | 1998-04-21 | Shinotesuto:Kk | 形質転換体にて発現される蛋白質に含まれる夾雑物質の除去方法及び精製蛋白質 |
DE69737479T4 (de) * | 1996-08-30 | 2010-05-06 | Novo Nordisk A/S | Glp-1 derivate |
RU2180218C2 (ru) | 1997-01-20 | 2002-03-10 | Джапэн Энерджи Корпорейшн | Способ стабилизации гирудина и/или вариантов гирудина, лиофилизированная фармацевтическая композиция, полученная с применением данного способа |
CA2236519C (en) * | 1997-05-02 | 2011-09-13 | 1149336 Ontario Inc. | Methods of enhancing functioning of the large intestine |
CO4750643A1 (es) | 1997-06-13 | 1999-03-31 | Lilly Co Eli | Formulacion estable de la insulina que contiene l-arginina y protamina |
EP1029536B1 (en) | 1997-10-01 | 2007-11-28 | Novadel Pharma Inc. | Buccal non-polar spray |
ATE237636T1 (de) | 1997-10-24 | 2003-05-15 | Genentech Inc | Reinigung von molekülen |
JP2001525371A (ja) | 1997-12-05 | 2001-12-11 | イーライ・リリー・アンド・カンパニー | Glp−1製剤 |
DE29721752U1 (de) | 1997-12-09 | 1998-02-12 | Siemens Ag | Crimpkontakt für Stecksysteme |
AU2610799A (en) * | 1998-02-27 | 1999-09-15 | Novo Nordisk A/S | Glp-1 derivatives with helix-content exceeding 25 per cent, forming partially structured micellar-like aggregates |
ATE466027T1 (de) * | 1998-02-27 | 2010-05-15 | Novo Nordisk As | Abkömmlinge von glp-1 analogen |
AU3247799A (en) * | 1998-02-27 | 1999-09-15 | Novo Nordisk A/S | Glp-1 derivatives of glp-1 and exendin with protracted profile of action |
ATE466028T1 (de) | 1998-02-27 | 2010-05-15 | Novo Nordisk As | N-terminal veränderte glp-1 abkömmlinge |
WO1999057566A1 (en) * | 1998-05-01 | 1999-11-11 | The University Of Tennessee Research Corporation | Flow cytometric characterization of amyloid fibrils |
CN1317967A (zh) * | 1998-09-17 | 2001-10-17 | 伊莱利利公司 | 蛋白质制剂 |
WO2000037098A1 (en) * | 1998-12-22 | 2000-06-29 | Eli Lilly And Company | Shelf-stable formulation of glucagon-like peptide-1 |
CA2356706C (en) | 1999-01-14 | 2014-09-30 | Amylin Pharmaceuticals, Inc. | Novel exendin agonist formulations and methods of administration thereof |
US6444788B1 (en) * | 1999-03-15 | 2002-09-03 | Novo Nordisk A/S | Ion exchange chromatography of GLP-1, analogs and derivatives thereof |
EP1956000B1 (en) * | 1999-03-17 | 2016-10-05 | Novo Nordisk A/S | Acylating agents useful for acylating peptides |
AU5760900A (en) | 1999-06-25 | 2001-01-31 | Minimed, Inc. | Multiple agent diabetes therapy |
EP1076066A1 (en) | 1999-07-12 | 2001-02-14 | Zealand Pharmaceuticals A/S | Peptides for lowering blood glucose levels |
US6569832B1 (en) * | 1999-11-12 | 2003-05-27 | Novo Nordisk A/S | Inhibition of beta cell degeneration |
JP2003523972A (ja) | 1999-12-16 | 2003-08-12 | イーライ・リリー・アンド・カンパニー | 安定性が改良されたポリペプチド組成物 |
US7022674B2 (en) * | 1999-12-16 | 2006-04-04 | Eli Lilly And Company | Polypeptide compositions with improved stability |
GB9930882D0 (en) | 1999-12-30 | 2000-02-23 | Nps Allelix Corp | GLP-2 formulations |
AU2353701A (en) | 2000-01-11 | 2001-07-24 | Novo Nordisk A/S | Transepithelial delivery of glp-1 derivatives |
AU2001220765A1 (en) | 2000-01-24 | 2001-07-31 | Medtronic Minimed, Inc. | Mixed buffer system for stabilizing polypeptide formulations |
EP1396499A3 (en) | 2000-01-27 | 2004-12-29 | Eli Lilly And Company | Process for solubilizing glucagon-like peptide 1 (GLP-1) compounds |
DE60102899T2 (de) * | 2000-01-27 | 2005-03-31 | Eli Lilly And Co., Indianapolis | Verfahren zur lösung von glucagon-ähnlichen peptid-1 (glp-1) verbindungen |
US6569901B2 (en) * | 2000-01-28 | 2003-05-27 | Novo Nordisk A/S | Alkynyl-substituted propionic acid derivatives, their preparation and use |
US6844321B2 (en) * | 2000-01-31 | 2005-01-18 | Novo Nordisk A/S | Crystallization of a GLP-1 analogue |
WO2001077141A1 (en) | 2000-04-06 | 2001-10-18 | Novo Nordisk A/S | Shock heat treatment of polypeptides |
ATE346093T1 (de) * | 2000-06-16 | 2006-12-15 | Lilly Co Eli | Analoge des glucagon ähnlichen peptid-1 |
JP4798833B2 (ja) | 2000-10-24 | 2011-10-19 | 一般財団法人化学及血清療法研究所 | 加熱処理工程を含むヒト血清アルブミンの製造方法 |
MXPA03005135A (es) | 2000-12-13 | 2003-12-04 | Lilly Co Eli | Regimen de tratamiento cronico usando peptidos insulinotropicos similares al glucagon. |
WO2002048192A2 (en) | 2000-12-13 | 2002-06-20 | Eli Lilly And Company | Amidated glucagon-like peptide-1 |
US20020151467A1 (en) * | 2000-12-21 | 2002-10-17 | Leung Frank K. | Methods and compositions for oral insulin delivery |
GB2371227A (en) | 2001-01-10 | 2002-07-24 | Grandis Biotech Gmbh | Crystallisation - resistant aqueous growth hormone formulations |
US7112567B2 (en) * | 2001-02-16 | 2006-09-26 | Conjuchem Inc. | Long lasting glucagon-like peptide 2 (glp-2) for the treatment of gastrointestinal diseases and disorders |
WO2002069994A2 (en) | 2001-03-07 | 2002-09-12 | Novo Nordisk A/S | Combined use of derivatives of glp-1 analogs and ppar ligands |
US6573237B2 (en) * | 2001-03-16 | 2003-06-03 | Eli Lilly And Company | Protein formulations |
WO2002098445A1 (en) | 2001-05-30 | 2002-12-12 | Chugai Seiyaku Kabushiki Kaisha | Protein preparation |
WO2003002136A2 (en) * | 2001-06-28 | 2003-01-09 | Novo Nordisk A/S | Stable formulation of modified glp-1 |
CN1335182A (zh) | 2001-08-08 | 2002-02-13 | 华中科技大学 | 胰岛素口腔喷剂及其制备工艺 |
EP1432430A4 (en) * | 2001-08-28 | 2006-05-10 | Lilly Co Eli | PREMIXTURES OF GLP-1 AND BASALINSULIN |
JP2005508360A (ja) | 2001-10-19 | 2005-03-31 | イーライ・リリー・アンド・カンパニー | Glp−1およびインスリンの二相混合物 |
PT1344533E (pt) | 2002-03-15 | 2007-01-31 | Natimmune As | Composições farmacêuticas compreendendo lectina de ligação a manose |
US7273921B2 (en) * | 2002-09-25 | 2007-09-25 | Novo Nordisk A/S | Method for producing acylated peptides |
ES2308029T3 (es) | 2002-09-25 | 2008-12-01 | Novo Nordisk A/S | Proceso de purificacion que comprende una microfiltracion a temperaturas elevadas. |
WO2004089985A1 (en) * | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | Stable pharmaceutical compositions |
ES2425221T3 (es) | 2003-05-30 | 2013-10-14 | Amylin Pharmaceuticals, Llc | Nuevos métodos y composiciones para suministro por vía transmucosa potenciado de péptidos y proteínas |
PL1633390T3 (pl) | 2003-06-03 | 2012-06-29 | Novo Nordisk As | Stabilizowane kompozycje farmaceutyczne peptydu glp-1 |
US20060287221A1 (en) * | 2003-11-13 | 2006-12-21 | Novo Nordisk A/S | Soluble pharmaceutical compositions for parenteral administration comprising a GLP-1 peptide and an insulin peptide of short time action for treatment of diabetes and bulimia |
ATE525083T1 (de) | 2003-11-13 | 2011-10-15 | Novo Nordisk As | Pharmazeutische zusammensetzung umfassend eine insulinotrope glp-1(7-37) analoge, asp(b28)- insulin, und eine oberflächenaktive verbindung |
MXPA06005581A (es) * | 2003-11-20 | 2006-08-11 | Novo Nordisk As | Formulaciones de peptidos que contienen propilenglicol que son optimas para la produccion y uso en dispositivos de inyeccion. |
WO2006025882A2 (en) | 2004-08-25 | 2006-03-09 | The Uab Research Foundation | Absorption enhancers for drug administration |
EP1814581B1 (en) * | 2004-11-12 | 2016-03-16 | Novo Nordisk A/S | Stable formulations of peptides comprising an acylated glp-1 analogue and a basal insuline |
EP2049567A2 (en) * | 2006-07-18 | 2009-04-22 | Centocor, Inc. | Human glp-1 mimetibodies, compositions, methods and uses |
TW200843794A (en) * | 2006-12-21 | 2008-11-16 | Centocor Inc | Use of long-acting GLP-1 receptor agonists to improve insulin sensitivity and lipid profiles |
-
2002
- 2002-06-27 WO PCT/DK2002/000437 patent/WO2003002136A2/en active IP Right Grant
- 2002-06-27 JP JP2003508375A patent/JP5562510B2/ja not_active Expired - Lifetime
- 2002-06-27 EP EP02745182A patent/EP1412384B1/en not_active Expired - Lifetime
- 2002-06-27 PT PT02745182T patent/PT1412384E/pt unknown
- 2002-06-27 DE DE60224284T patent/DE60224284T2/de not_active Expired - Lifetime
- 2002-06-27 AT AT02745182T patent/ATE382057T1/de active
- 2002-06-27 US US10/185,923 patent/US20030119734A1/en not_active Abandoned
- 2002-06-27 DK DK02745182T patent/DK1412384T3/da active
- 2002-06-27 ES ES02745182T patent/ES2298378T3/es not_active Expired - Lifetime
- 2002-06-27 AU AU2002316811A patent/AU2002316811A1/en not_active Abandoned
-
2007
- 2007-04-11 US US11/786,095 patent/US20080167226A1/en not_active Abandoned
-
2008
- 2008-12-24 US US12/343,722 patent/US20090111752A1/en not_active Abandoned
-
2010
- 2010-05-24 US US12/785,861 patent/US8846618B2/en not_active Expired - Lifetime
-
2011
- 2011-09-26 JP JP2011209396A patent/JP2012051894A/ja not_active Withdrawn
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5652216A (en) * | 1994-05-26 | 1997-07-29 | Novo Nordisk A/S | Pharmaceutical preparation |
US5869602A (en) * | 1995-03-17 | 1999-02-09 | Novo Nordisk A/S | Peptide derivatives |
US6268343B1 (en) * | 1996-08-30 | 2001-07-31 | Novo Nordisk A/S | Derivatives of GLP-1 analogs |
US6380357B2 (en) * | 1997-12-16 | 2002-04-30 | Eli Lilly And Company | Glucagon-like peptide-1 crystals |
US6384016B1 (en) * | 1998-03-13 | 2002-05-07 | Novo Nordisk A/S | Stabilized aqueous peptide solutions |
US20030220255A1 (en) * | 2002-04-04 | 2003-11-27 | Knudsen Liselotte Bjerre | GLP-1 agonist and cardiovascular complications |
Cited By (72)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040037818A1 (en) * | 1998-07-30 | 2004-02-26 | Brand Stephen J. | Treatment for diabetes |
US20040209816A1 (en) * | 1999-01-29 | 2004-10-21 | Indu Parikh | Treatment for diabetes |
US20090041731A1 (en) * | 1999-01-29 | 2009-02-12 | Indu Parikh | Treatment for Diabetes |
US8846618B2 (en) | 2001-06-28 | 2014-09-30 | Novo Nordisk A/S | Stable formulation of modified GLP-1 |
US20100234299A1 (en) * | 2001-06-28 | 2010-09-16 | Novo Nordisk A/S | Stable formulation of modified glp-1 |
US20060093660A1 (en) * | 2002-02-27 | 2006-05-04 | Bolotin Elijah M | Compositions for treatment with glucagon-like peptide, and methods of making and using the same |
US8277776B2 (en) | 2002-02-27 | 2012-10-02 | Pharmain Corporation | Compositions for delivery of therapeutics and other materials |
US7589169B2 (en) | 2002-02-27 | 2009-09-15 | Pharmain Corporation | Compositions for treatment with glucagon-like peptide, and methods of making and using the same |
US20100158806A1 (en) * | 2002-02-27 | 2010-06-24 | Bolotin Elijah M | Compositions for Delivery of Therapeutics and Other Materials |
US20060239924A1 (en) * | 2002-02-27 | 2006-10-26 | Bolotin Elijah M | Compositions for delivery of therapeutics and other materials, and methods of making and using the same |
US7635463B2 (en) | 2002-02-27 | 2009-12-22 | Pharmain Corporation | Compositions for delivery of therapeutics and other materials |
US8231859B2 (en) | 2002-02-27 | 2012-07-31 | Pharmain Corporation | Compositions for delivery of therapeutics and other materials |
US20080015263A1 (en) * | 2002-02-27 | 2008-01-17 | Bolotin Elijah M | Compositions for delivery of therapeutics and other materials |
US8257682B2 (en) | 2002-02-27 | 2012-09-04 | Pharmain Corporation | Compositions for delivery of therapeutics and other materials |
US7790140B2 (en) | 2002-02-27 | 2010-09-07 | Pharmain Corporation | Compositions for delivery of therapeutics and other materials, and methods of making and using the same |
US20100221184A1 (en) * | 2002-02-27 | 2010-09-02 | Bolotin Elijah M | Compositions for Delivery of Therapeutics and Other Materials |
US20060234373A1 (en) * | 2002-05-24 | 2006-10-19 | Alex Rabinovitch | Treatment for diabetes |
US7560425B2 (en) | 2002-06-07 | 2009-07-14 | Waratah Pharmaceuticals Inc. | Pharmaceutical composition consisting of rapamycine and gastrin 17(LEU15) and a method for treating diabetes |
US20040209801A1 (en) * | 2002-10-22 | 2004-10-21 | Brand Stephen J. | Treatment of diabetes |
US20080318865A1 (en) * | 2003-06-03 | 2008-12-25 | Novo Nordisk A/S | Stabilized Pharmaceutical Peptide Compositions |
US8614181B2 (en) | 2003-06-03 | 2013-12-24 | Novo Nordisk A/S | Stabilized pharmaceutical peptide compositions |
US8114959B2 (en) | 2003-06-03 | 2012-02-14 | Novo Nordisk A/S | Stabilized pharmaceutical peptide compositions |
US20100056451A1 (en) * | 2003-06-03 | 2010-03-04 | Novo Nordisk A/S | Stabilized Pharmaceutical Peptide Compositions |
US20100184687A1 (en) * | 2003-08-21 | 2010-07-22 | Novo Nordisk A/S | Purification of Glucagon-Like Peptides |
US20060211616A1 (en) * | 2003-08-21 | 2006-09-21 | Novo Nordisk A/S | Purification of glucagon-like peptides |
US20100190715A1 (en) * | 2003-09-01 | 2010-07-29 | Novo Nordisk A/S | Stable Formulations of Peptides |
US20060247167A1 (en) * | 2003-09-01 | 2006-11-02 | Novo Nordisk A/S | Stable formulations of peptides |
US8114833B2 (en) | 2003-11-20 | 2012-02-14 | Novo Nordisk A/S | Propylene glycol-containing peptide formulations which are optimal for production and for use in injection devices |
US20070010424A1 (en) * | 2003-11-20 | 2007-01-11 | Novo Nordisk A/S | Propylene glycol-containing peptide formulations which are optimal for production and for use in injection devices |
US20050143303A1 (en) * | 2003-12-26 | 2005-06-30 | Nastech Pharmaceutical Company Inc. | Intranasal administration of glucose-regulating peptides |
US20060074025A1 (en) * | 2003-12-26 | 2006-04-06 | Nastech Pharmaceutical Company Inc. | Therapeutic formulations for transmucosal administration that increase glucagon-like peptide-1 bioavailability |
US20080318837A1 (en) * | 2003-12-26 | 2008-12-25 | Nastech Pharmaceutical Company Inc. | Pharmaceutical Formation For Increased Epithelial Permeability of Glucose-Regulating Peptide |
US20080234200A1 (en) * | 2003-12-26 | 2008-09-25 | Nastech Pharmaceutical Company Inc. | Method of treatment of a metabolic disease using intranasal administration of exendin peptide |
US20090202494A1 (en) * | 2004-01-30 | 2009-08-13 | Antonio Cruz | Combined use of glp-1 agonists and gastrin for regulating blood glucose levels |
US20050260259A1 (en) * | 2004-04-23 | 2005-11-24 | Bolotin Elijah M | Compositions for treatment with glucagon-like peptide, and methods of making and using the same |
US20080171848A1 (en) * | 2004-08-31 | 2008-07-17 | Novo Nordisk A/S | Use of Tris(Hydroxymethyl) Aminomethane For the Stabilization of Peptides, Polypeptides and Proteins |
US8710181B2 (en) | 2004-08-31 | 2014-04-29 | Novo Nordisk A/S | Use of tris(hydroxymethyl) aminomethane for the stabilization of peptides, polypeptides and proteins |
US8748376B2 (en) * | 2004-11-12 | 2014-06-10 | Novo Nordisk A/S | Stable formulations of peptides |
US20100173844A1 (en) * | 2004-11-12 | 2010-07-08 | Novo Nordisk A/S | Stable Formulations of Peptides |
US20080318861A1 (en) * | 2005-12-08 | 2008-12-25 | Nastech Pharmaceutical Company Inc. | Mucosal Delivery of Stabilized Formulations of Exendin |
US10507248B2 (en) | 2005-12-19 | 2019-12-17 | Pharmain Corporation | Hydrophobic core carrier compositions for delivery of therapeutic agents, methods of making and using the same |
US9737615B2 (en) | 2005-12-19 | 2017-08-22 | PharmalN Corporation | Hydrophobic core carrier compositions for delivery of therapeutic agents, methods of making and using the same |
US20110207662A1 (en) * | 2007-08-03 | 2011-08-25 | Pharmain Corporation | Composition for Long-Acting Peptide Analogs |
US9657078B2 (en) | 2007-08-03 | 2017-05-23 | Pharmain Corporation | Composition for long-acting peptide analogs |
US8518876B2 (en) | 2007-08-03 | 2013-08-27 | PharmalN Corporation | Composition for long-acting peptide analogs |
US7960336B2 (en) | 2007-08-03 | 2011-06-14 | Pharmain Corporation | Composition for long-acting peptide analogs |
US20090088387A1 (en) * | 2007-08-03 | 2009-04-02 | Pharmain Corporation | Composition for long-acting peptide analogs |
US9090664B2 (en) | 2007-08-03 | 2015-07-28 | Pharmain Corporation | Composition for long-acting peptide analogs |
US20090053169A1 (en) * | 2007-08-20 | 2009-02-26 | Pharmain Corporation | Oligonucleotide Core Carrier Compositions for Delivery of Nucleic Acid-Containing Therapeutic Agents, Methods of Making and Using the Same |
US8563527B2 (en) | 2007-08-20 | 2013-10-22 | Pharmain Corporation | Oligonucleotide core carrier compositions for delivery of nucleic acid-containing therapeutic agents, methods of making and using the same |
US20090176892A1 (en) * | 2008-01-09 | 2009-07-09 | Pharmain Corporation | Soluble Hydrophobic Core Carrier Compositions for Delivery of Therapeutic Agents, Methods of Making and Using the Same |
US9562111B2 (en) | 2008-01-09 | 2017-02-07 | Pharmain Corporation | Soluble hydrophobic core carrier compositions for delivery of therapeutic agents, methods of making and using the same |
US8999930B2 (en) | 2008-01-09 | 2015-04-07 | Pharmain Corporation | Soluble hydrophobic core carrier compositions for delivery of therapeutic agents, methods of making and using the same |
US9168288B2 (en) | 2010-04-09 | 2015-10-27 | Mount Sinai Hospital | Methods for treating disorders of the gastrointestinal tract using a GLP-1 agonist |
WO2011123943A1 (en) | 2010-04-09 | 2011-10-13 | Mount Sinai Hospital | Methods for treating disorders of the gastrointestinal tract using a glp-1 agonist |
US10758592B2 (en) | 2012-10-09 | 2020-09-01 | Sanofi | Exendin-4 derivatives as dual GLP1/glucagon agonists |
US9670261B2 (en) | 2012-12-21 | 2017-06-06 | Sanofi | Functionalized exendin-4 derivatives |
US9745360B2 (en) | 2012-12-21 | 2017-08-29 | Sanofi | Dual GLP1/GIP or trigonal GLP1/GIP/glucagon agonists |
US10253079B2 (en) | 2012-12-21 | 2019-04-09 | Sanofi | Functionalized Exendin-4 derivatives |
US9750788B2 (en) | 2013-12-13 | 2017-09-05 | Sanofi | Non-acylated exendin-4 peptide analogues |
US9789165B2 (en) | 2013-12-13 | 2017-10-17 | Sanofi | Exendin-4 peptide analogues as dual GLP-1/GIP receptor agonists |
US9751926B2 (en) | 2013-12-13 | 2017-09-05 | Sanofi | Dual GLP-1/GIP receptor agonists |
US9694053B2 (en) | 2013-12-13 | 2017-07-04 | Sanofi | Dual GLP-1/glucagon receptor agonists |
US9771406B2 (en) | 2014-04-07 | 2017-09-26 | Sanofi | Peptidic dual GLP-1/glucagon receptor agonists derived from exendin-4 |
US9775904B2 (en) | 2014-04-07 | 2017-10-03 | Sanofi | Exendin-4 derivatives as peptidic dual GLP-1/glucagon receptor agonists |
US9758561B2 (en) | 2014-04-07 | 2017-09-12 | Sanofi | Dual GLP-1/glucagon receptor agonists derived from exendin-4 |
US9932381B2 (en) | 2014-06-18 | 2018-04-03 | Sanofi | Exendin-4 derivatives as selective glucagon receptor agonists |
US10806797B2 (en) | 2015-06-05 | 2020-10-20 | Sanofi | Prodrugs comprising an GLP-1/glucagon dual agonist linker hyaluronic acid conjugate |
US9982029B2 (en) | 2015-07-10 | 2018-05-29 | Sanofi | Exendin-4 derivatives as selective peptidic dual GLP-1/glucagon receptor agonists |
US11752198B2 (en) | 2017-08-24 | 2023-09-12 | Novo Nordisk A/S | GLP-1 compositions and uses thereof |
CN112912100A (zh) * | 2018-10-26 | 2021-06-04 | 诺和诺德股份有限公司 | 稳定的司美鲁肽组合物及其用途 |
US11318191B2 (en) | 2020-02-18 | 2022-05-03 | Novo Nordisk A/S | GLP-1 compositions and uses thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2004535442A (ja) | 2004-11-25 |
JP5562510B2 (ja) | 2014-07-30 |
ATE382057T1 (de) | 2008-01-15 |
US20090111752A1 (en) | 2009-04-30 |
US20080167226A1 (en) | 2008-07-10 |
US8846618B2 (en) | 2014-09-30 |
PT1412384E (pt) | 2008-03-28 |
JP2012051894A (ja) | 2012-03-15 |
ES2298378T3 (es) | 2008-05-16 |
EP1412384A2 (en) | 2004-04-28 |
DE60224284D1 (de) | 2008-02-07 |
US20100234299A1 (en) | 2010-09-16 |
AU2002316811A1 (en) | 2003-03-03 |
WO2003002136A2 (en) | 2003-01-09 |
EP1412384B1 (en) | 2007-12-26 |
WO2003002136A3 (en) | 2004-03-04 |
DE60224284T2 (de) | 2008-12-18 |
DK1412384T3 (da) | 2008-04-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8846618B2 (en) | Stable formulation of modified GLP-1 | |
US7632806B2 (en) | Stabilized pharmaceutical peptide compositions | |
US7235627B2 (en) | Derivatives of GLP-1 analogs | |
US8114959B2 (en) | Stabilized pharmaceutical peptide compositions | |
AU2004243531B2 (en) | Stabilized pharmaceutical peptide compositions | |
US20060183682A1 (en) | Stabilized pharmaceutical peptide compositions | |
US7595293B2 (en) | Stable pharmaceutical compositions | |
US6458924B2 (en) | Derivatives of GLP-1 analogs | |
JP5248113B2 (ja) | ペプチドの安定な処方 | |
US20040122210A1 (en) | GLP-2 compounds, formulations, and uses thereof | |
US20090011987A1 (en) | Use of Glp-2 for the Treatment of Ischemia-Reperfusion Injury |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: NOVO NORDISK A/S, DENMARK Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:FLINK, JAMES M.;LARSEN, SILKE MOLLER;JENSEN, SIMON BJERREGAARD;AND OTHERS;REEL/FRAME:013395/0205;SIGNING DATES FROM 20020829 TO 20020918 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |