IP Library Granted Patent US 10,485,872
Granted Patent B2
US 10,485,872 · App. 16/173,299 · Granted Nov 26, 2019

Pharmaceutical composition containing pyridylaminoacetic acid compound

Inventor: Yoko Endo (Ikoma, JP)
Assignee: SANTEN PHARMACEUTICAL CO., LTD.
A61K47/183A61K9/0048A61K31/444A61K47/22A61K47/26A61K47/44A61K47/02A61K47/12Y02A50/465
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Quick Facts
Patent No.
US 10,485,872
App. No.
16/173,299
Granted
Nov 26, 2019
Kind
B2
Abstract

The purpose of the present invention is to provide a pharmaceutical composition that comprises a specific compound and exhibits a superior preservation efficacy, the specific compound being stable within the pharmaceutical composition, and to provide methods for improving the stability of the specific compound within the pharmaceutical composition and the preservation efficacy of the pharmaceutical composition. The pharmaceutical composition according to the present invention comprises isopropyl (6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino)acetate or a salt thereof, and further comprises edetic acid or a salt thereof.

Claims (17)

1. A pharmaceutical composition comprising isopropyl (6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino)acetate or a salt thereof and a nonionic surfactant, which further comprises edetic acid or a salt thereof, wherein the nonionic surfactant includes polyoxyethylene hardened castor oil;

wherein the content of the nonionic surfactant is in a range of 0.001 to 5% (w/v); and

wherein the content of edetic acid or a salt thereof is in a range of 0.001 to 1% (w/v).

2. The pharmaceutical composition according to claim 1 , wherein the polyoxyethylene hardened castor oil includes polyoxyethylene hardened castor oil selected from the group consisting of polyoxyethylene hardened castor oil 10, polyoxyethylene hardened castor oil 40, polyoxyethylene hardened castor oil 50, and polyoxyethylene hardened castor oil 60.

3. The pharmaceutical composition according to claim 1 , wherein the content of the nonionic surfactant is in a range of 0.5 to 3% (w/v).

4. The pharmaceutical composition according to claim 1 , wherein the content of the nonionic surfactant is in a range of 1 to 20,000 parts by mass relative to 1 part by mass of isopropyl 6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino) acetate or a salt thereof.

5. The pharmaceutical composition according to claim 1 , wherein the content of isopropyl 6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino) acetate or a salt thereof is in a range of 0.0001 to 0.1% (w/v).

6. The pharmaceutical composition according to claim 5 , wherein the content of isopropyl 6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino) acetate or a salt thereof is in a range of 0.001 to 0.003% (w/v).

7. The pharmaceutical composition according to claim 1 , wherein the content of edetic acid or a salt thereof is in a range of 0.01 to 0.1% (w/v).

8. The pharmaceutical composition according to claim 1 , wherein the content of edetic acid or a salt thereof is in a range of 0.1 to 1,000 parts by mass relative to 1 part by mass of isopropyl 6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino) acetate or a salt thereof.

9. The pharmaceutical composition according to claim 1 , which further comprises boric acid or a salt thereof, citric acid or a salt thereof, or acetic acid or a salt thereof.

10. The pharmaceutical composition according to claim 1 , which does not comprise sorbic acid.

11. The pharmaceutical composition according to claim 1 , which is filled into a container made of polyethylene.

12. The pharmaceutical composition according to claim 1 , for prevention or treatment of glaucoma or ocular hypertension, or for reduction of intraocular pressure.

13. A method for stabilizing isopropyl (6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino)acetate or a salt thereof comprising adding edetic acid or a salt thereof and polyoxyethylene hardened castor oil into a pharmaceutical composition comprising isopropyl (6-{[4-(pyrazol-1-yl)benzyl](pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-ylamino)acetate or a salt thereof;

wherein the content of the nonionic surfactant is in a range of 0.001 to 5% (w/v); and

wherein the content of edetic acid or a salt thereof is in a range of 0.001 to 1 (w/v).

Assignments (2)
ADDRESS CHANGE Recorded Mar 17, 2022
From: SANTEN PHARMACEUTICAL CO., LTD.
To: SANTEN PHARMACEUTICAL CO., LTD.
Reel/Frame 059422/0276 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 29, 2018
From: ENDO, YOKO
To: SANTEN PHARMACEUTICAL CO., LTD.
Reel/Frame 047339/0340 →
Priority Claims (1)
JP 2014-002810 · Jan 10, 2014 · national
Continuity (3)
Continuation 15204507 · Jul 7, 2016
Continuation PCTJP2015050334 · Jan 8, 2015
Related Publication 20190060459A1 · Feb 28, 2019
Cited By (2)
US 12,636,367 US 12,678,429