IP Library › Granted Patent US 9,517,266
Granted Patent B2
US 9,517,266 · App. 14/231,580 · Granted Dec 13, 2016

Liquid formulation containing a protein drug

Inventors: In Hwan Lim (Suwon-si, KR); Dong Uk Kim (Yongin-si, KR); Geun Woong Kim (Yongin-si, KR); Hee Kyung Sung (Daejeon, KR); Yun Ju Jeong (Hwaseong-si, KR)
Assignee: SAMSUNG ELECTRONICS CO., LTD.
A61K39/39591A61K9/0019A61K9/08A61K47/183A61K47/26C07K16/2863C07K2317/14C07K2317/24C07K2317/52C07K2317/53C07K2317/565C07K2317/92
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Quick Facts
Patent No.
US 9,517,266
App. No.
14/231,580
Granted
Dec 13, 2016
Kind
B2
Abstract

Disclosed is a method of preparing a stabilized liquid formulation of a protein drug, comprising admixing a protein drug with a composition for stabilization, wherein the composition for stabilization comprises a surfactant, a buffer, and a liquid medium, and has a pH from about 5 to about 8.

Claims (13)

1. A method for stabilizing a protein drug, comprising admixing a protein drug with a composition for stabilization, wherein the composition for stabilization comprises a surfactant, a buffer, and a liquid medium, and has a pH from about 5 to about 8, wherein the protein drug is an anti-c-Met antibody or antigen-binding fragment thereof comprising a CDR-H1 comprising SEQ ID NO: 1, a CDR-H2 comprising SEQ ID NO: 2, a CDR-H3 comprising SEQ ID NO: 3, a CDR-L1 comprising SEQ ID NO: 10, a CDR-L2 comprising SEQ ID NO: 11, and a CDR-L3 comprising SEQ ID NO: 13; and the buffer comprises succinic acid, citric acid, or a combination thereof.

2. The method according to claim 1 , wherein the surfactant comprises one or more selected from the group consisting of polysorbate, poloxamer, polyethylene-polypropylene glycol, polyoxyethylene, and sodium dodecyl sulphate.

3. The method according to claim 2 , wherein the surfactant comprises one or more selected from the group consisting of polysorbate 20, polysorbate 40, polysorbate 60, and polysorbate 80.

4. The method according to claim 1 , wherein the amount of the surfactant in the composition for stabilization is about 0.01% to about 1% (w/v) based on the total amount of the composition for stabilization.

5. The method according to claim 1 , wherein the composition for stabilization has a pH from about 5 to about 7.

6. The method according to claim 1 , wherein the amount of the buffer in the composition for stabilization is about 0.1 to about 1% (w/v) based on the total amount of the composition for stabilization.

7. The method according to claim 1 , wherein the composition for stabilization has an osmotic pressure of about 250 to about 400 milliosmole (mOsm).

8. The method according to claim 1 , wherein the composition for stabilization further comprises an osmoregulating agent selected from the group consisting of a pharmaceutically acceptable salt, a sugar, an amino acid, and any combination thereof.

9. The method according to claim 8 , wherein the osmoregulating agent comprises one or more selected from the group consisting of sodium chloride, sodium succinate, sodium sulfate, potassium chloride, magnesium chloride, magnesium sulfate, trehalose, sucrose, mannitol, sorbitol, fructose, maltose, lactose, dextran, proline, alanine, arginine, asparagine, aspartic acid, glycine, serine, lysine, and histidine.

10. The method according to claim 8 , wherein the amount of the osmo-regulating agent in the composition for stabilization is about 0.01 to about 1% (w/v) based on the total amount of the composition for stabilization.

11. The method according to claim 1 , wherein the amount of the protein drug in the liquid formulation is about 1 mg/ml to about 200 mg/ml.

12. The method according to claim 1 , wherein about 5% or less of the initial protein drug content of the liquid formulation aggregates or degrades after the liquid formulation has been stored at about 40° C. to about 50° C. for three months.

13. The method of claim 1 , wherein the anti-c-Met antibody comprises a heavy chain comprising the amino acid sequence from the 18 th to 460 th positions of SEQ ID NO: 66 and a light chain comprising the amino acid sequence from the 21 st to 240 th positions of SEQ ID NO: 68.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2014
From: LIM, IN HWAN; KIM, DONG UK; KIM, GEUN WOONG; SUNG, HEE KYUNG; JEONG, YUN JU
To: SAMSUNG ELECTRONICS CO., LTD.
Reel/Frame 032769/0990 →
Priority Claims (1)
KR 10-2013-0034893 · Mar 29, 2013 · national
Continuity (1)
Related Publication 20140303357A1 · Oct 9, 2014