INSULIN WITH A BASAL RELEASE PROFILE

• US 20100069292A1
• Filed: 09/02/2009
• Published: 03/18/2010
• Est. Priority Date: 09/02/2008
• Status: Abandoned Application

• Current Assignee: Biodel Inc. (Ipsen Sa)
• Original Assignee: Biodel Inc. (Ipsen Sa)
• Inventors: Ozhan, Koray, Steiner, Solomon S., Pohl, Roderike, Kashyap, Nandini, Hauser, Robert
• Application Number:
  US12/552,855
• Publication Number:
  US 20100069292A1
• Time in Patent Office: Days
• US Class Current: 514/5.900
• CPC Class Codes: A61K 38/28 Insulins
• CPC Class Codes: A61K 47/02 Inorganic compounds
• CPC Class Codes: A61K 47/183 Amino acids, e.g. glycine, EDTA or aspartame
• CPC Class Codes: A61K 9/0019 Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner non-active ingredients are additionally classified in A61K47/00

Abstract

A clear basal insulin formulation composed of insulin (preferably human recombinant insulin), buffering agents, precipitating agents, and/or stabilizing agents for subcutaneous, intradermal or intramuscular administration. The formulation is designed to form a precipitate of insulin following injection, creating a slow releasing “basal insulin” over a period of 12 to 24 hours, which can be varied by compositional changes to tailor the release profile to the needs of the individual diabetic patient

Claims

1. A basal insulin formulation comprising a solution of recombinant human insulin at a pH between 3.5 and 4.5, preferably 3.8 to 4.2, or 7.5 to 8.5, optionally in combination with a stabilizing agent, buffering agent and precipitating agent, but not including protamine.

2. The formulation of claim 1, in the form of a clear solution having a pH greater than 7.5, which forms a precipitate at physiological pH.

3. The formulation of claim 1, further comprising an insulin analog.

4. The formulation of claim 1 comprising a stabilizing agent which maintains the insulin as a hexamer, preferably zinc at a concentration of 50 micrograms or less.

5. The formulation of claim 1 comprising precipitating agent selected from the group consisting of buffering agents, solubility modifying agents, precipitation seeding agents, and precipitation enhancing agents.

6. The formulation of claim 5, comprising a precipitation enhancing agent selected from the group consisting of zinc acetate, zinc oxide, zinc citrate, zinc carbonate, zinc sulfate, or zinc chloride, calcium chloride and other divalent salts used at non-toxic levels.

7. The formulation of claim 6 comprising zinc chloride in a concentration range of 0.1 to 10 mg/mL, most preferably 2-3 mg/mL.

8. The formulation of claim 5 wherein the precipitating agent is a buffering agent, preferably selected from the group consisting of acetate, citrate, phosphate, carbonate, and barbital, most preferably sodium acetate in a concentration in the range of 0.2 to 20mg/mL, preferably from 1 to 10 mg/mL, most preferably between 5 and 6 mg/mL.

9. The formulation of claim 5 wherein the precipitating agent is a solubility modifying agent, preferably a charged amino acid, more preferably selected from the group consisting of arginine, histidine, lysine, most preferably Arginine in the range of 0.005 to 10 mg/mL.

10. The formulation of claim 5 wherein the precipitating agent is a seeding agent selected from the group consisting of cysteine, L-proline and tyrosine, and nanoparticles such as C₆₀ or Au₁₂.

11. The formulation of claim 1, comprising at least one pH modifying agent selected from the group consisting of sodium hydroxide, citric acid, hydrochloric acid, acetic acid, phosphoric acid, succinic acid, sodium hydroxide, potassium hydroxide, ammonium hydroxide, magnesium oxide, calcium hydroxide, calcium carbonate, magnesium carbonate, magnesium aluminum silicates, malic acid, potassium citrate, sodium citrate, sodium phosphate, lactic acid, gluconic acid, tartaric acid, 1,2,3,4-butane tetracarboxylic acid, fumaric acid, diethanolamine, monoethanolamine, sodium carbonate, sodium bicarbonate, triethanolamine, and combinations thereof

12. The formulation of claim 1, containing a preservative.

13. The formulation of claim 1, provided in a kit consisting of two or more containers which are mixed at the time of administration to form an insulin solution at the time of injection.

14. The formulation of claim 1, providing a basal effective amount of insulin for a period of 12 to 24 hours following administered by subcutaneous, intramuscular, or intradermal injection.

15. The formulation of claim 1 providing an initial burst release of insulin.

16. The formulation of claim 15 providing sustained release of insulin over a period of 12 to 24 hours after an initial burst release.

17. The formulation of claim 1 providing a insulin basal release profile for a short, medium or long duration, preferably of 12 to 16 hours, 16 to 20, or 20 to 24 hours.

18. A method of providing a basal insulin to an individual in need thereof comprising administering the formulation of claim 1.

19. The method of claim 18 wherein the insulin is provided in a first container as a lyophilized powder which is reconstituted at the time of administration and the other ingredients are present in one or both of the vials.

20. The method of claim 19 wherein the contents of the two containers are mixed to form a clear solution prior to administration.