IP Library Granted Patent US 8,562,967
Granted Patent B2
US 8,562,967 · App. 12/675,776 · Granted Oct 22, 2013

Stable liquid formulations of G-CSF

Inventors: Walter Hinderer (Rodgau, DE); Heinz Lubenau (Neustadt, DE)
Assignee: Biogenerix AG
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Quick Facts
Patent No.
US 8,562,967
App. No.
12/675,776
Granted
Oct 22, 2013
Kind
B2
Abstract

Provided are pharmaceutical liquid formulations of G-CSF, which are stable over a long time period and substantially free of excipients, as well as ready-to-use syringes containing such formulations and corresponding kits.

Claims (25)

1. A medicament comprising an aqueous liquid formulation of G-CSF, the aqueous liquid formulation of G-CSF comprising G-CSF, sorbitol at a concentration of 5% w/v, polysorbate at a concentration of 0.05 to 0.06 mg/ml, and acetate at a concentration of 10 mM as a buffer substance at a pH value of 4.15 to 4.3.

2. A medicament according to claim 1 , wherein the G-CSF is non-glycosylated.

3. A medicament according to claim 1 , wherein the G-CSF is present at a concentration of 0.6 mg/ml.

4. A medicament according to claim 1 , which is substantially free of amino acids and/or additional protein.

5. A medicament according to claim 1 , which is an injection or infusion solution.

6. A medicament comprising an aqueous liquid formulation of G-CSF as injection or infusion solution, the aqueous liquid formulation of G-CSF consisting of human, non-glycosylated methionyl G-CSF at a concentration of 0.6 mg/ml and of sorbitol at a concentration of 5% (w/v), polysorbate 80 at a concentration of 0.05 to 0.06 mg/ml, and acetate at a concentration of 10 mM as a buffer substance at a pH value of 4.2±0.15.

7. A medicament according to claim 1 , for the treatment of cancer, severe chronic neutropenia (SCN ), HIV infection, a damage of the central nervous system, adverse side effects owing to cytotoxic chemotherapy, or for the accompanying therapy of diseases, wherein a mobilization of peripheral blood precursor cells is required.

8. A receptacle for the administration of liquid medicaments, comprising a liquid medicament formulation according to claim 1 .

9. A receptacle according to claim 8 , wherein at least one surface of said receptacle, which is in contact with the liquid formulation, is coated with a material consisting of silicone or polytetrafluoroethylene or an ethylene-tetrafluoroethylene (ETFE) copolymer.

10. A receptacle according to claim 8 , which is a syringe, an ampoule, a carpoule, or an infusion container.

11. The receptacle according to claim 10 , wherein the receptacle is a syringe or an ampoule, and wherein the liquid formulation is present, in terms of the concentration of G-CSF, at a concentration of 0.3 mg in a 0.5 ml or 0.48 mg in 0.8 ml.

12. A kit for the parenteral administration of G-CSF, comprising a receptacle according to claim 8 as well as instructions for storage and/or administration.

13. A kit according to claim 12 , wherein the administration of G-CSF is provided at a dosage of 5 to 30 μg/kg body weight.

14. A kit according to claim 12 , wherein 5 syringes or ampoules are provided in said kit.

15. A kit according to claim 12 , further comprising safety compartments for syringes and injection and/or infusion needles, respectively.

16. A kit according to claim 12 , wherein storage is intended at 5° C.

17. A medicament according to claim 1 , wherein the buffer substance is provided in the form of its free acid and the pH value of the solution is adjusted by the addition of a base.

18. A medicament according to claim 6 , wherein the medicament contains less than 1% oxidized species after storage for 4 weeks at 40° C. or 5° C.

19. A. medicament according to claim 1 , wherein the G-CSF is non-glycosylated and present at a concentration of 0.6 mg/ml and the pH value is 4.2 and wherein the medicament is substantially free of amino acids and/or additional proteins.

20. A receptacle for the administration of liquid medicaments, comprising the medicament according to claim 17 .

21. A receptacle according to claim 20 , wherein the receptacle is a syringe or an ampoule, and wherein the liquid formulation is present, in terms of the concentration of G-CSF, at a concentration of 0.3 mg in 0.5 ml or 0.48 mg in 0.8 ml.

22. The receptacle according to claim 21 , wherein at least one surface of said receptacle, which is in contact with the liquid formulation, is coated with a material consisting of silicone or polytetrafluoroethylene or an ethylene-tetrafluoroethylene (ETFE) copolymer.

23. A kit for the parentaral administration of G-CSF, comprising a receptacle according to claim 22 as well as instructions for storage and/or administration.

24. The medicament of claim 1 , further comprising an amino acid, glycerol, a carbohydrate, and/or a preservative.

25. A medicament according to claim 1 , wherein the medicament contains less than 1% oxidized species after storage for 4 weeks at 40° C. or 5° C.

Assignments (4)
MERGER Recorded May 2, 2014
From: BIOGENERIX GMBH
To: RATIOPHARM GMBH
Reel/Frame 032813/0427 →
CHANGE OF NAME Recorded May 2, 2014
From: BIOGENERIX AG
To: BIOGENERIX GMBH
Reel/Frame 032815/0845 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED ON REEL 024247 FRAME 0579. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNEE ADDRESS IS GRAF-ARCO-STR. 3, 89079 ULM, GERMANY. Recorded Oct 23, 2012
From: HINDERER, WALTER; LUBENAU, HEINZ
To: BIOGENERIX AG
Reel/Frame 029178/0217 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 16, 2010
From: HINDERER, WALTER; LUBENAU, HEINZ
To: BIOGENERIX AG
Reel/Frame 024247/0579 →
Priority Claims (2)
DE 10 2007 040 932 · Aug 27, 2007 · national
EP 07016763 · Aug 27, 2007 · regional
Continuity (1)
Related Publication 20100216698A1 · Aug 26, 2010