You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: November 22, 2024

Claims for Patent: 11,185,538


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 11,185,538
Title:Compositions for treating glaucoma or reducing intraocular pressure
Abstract: Described herein are compounds and compositions for treating glaucoma and/or reducing intraocular pressure. Compositions may comprise an isoquinoline compound and a prostaglandin or a prostaglandin analog. Compounds described herein include those in which an isoquinoline compound is covalently linked to a prostaglandin or a prostaglandin analog, and those in which an isoquinoline compound and a prostaglandin free acid together form a salt.
Inventor(s): Kopczynski; Casey (Chapel Hill, NC), Lin; Cheng-Wen (Raleigh, NC), Sturdivant; Jill Marie (Chapel Hill, NC), deLong; Mitchell A. (Chapel Hill, NC)
Assignee: Aerie Pharmaceuticals, Inc. (Bedminster, NJ)
Application Number:17/238,550
Patent Claims: 1. A pharmaceutical composition comprising about 0.01% (w/v) to about 1.0% (w/v) of a dimesylate salt of (S)-4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl 2,4-dimethylbenzoate and at least one excipient.

2. The pharmaceutical composition of claim 1, wherein the at least one excipient is a tonicity agent.

3. The pharmaceutical composition of claim 2, wherein the tonicity agent is mannitol.

4. The pharmaceutical composition of claim 3, wherein the mannitol is D-mannitol.

5. The pharmaceutical composition of claim 4, wherein the D-mannitol is about 4.7% (w/v) of the pharmaceutical composition.

6. The pharmaceutical composition of claim 2, further comprising a buffer.

7. The pharmaceutical composition of claim 6, wherein the buffer is boric acid and the pH of the pharmaceutical composition is about 5.0.

8. The pharmaceutical composition of claim 7, wherein the boric acid is about 0.05% (w/v) of the pharmaceutical composition.

9. The pharmaceutical composition of claim 5, further comprising a buffer.

10. The pharmaceutical composition of claim 9, wherein the buffer is boric acid and the pH of the pharmaceutical composition is about 5.0.

11. The pharmaceutical composition of claim 10, wherein the boric acid is about 0.05% (w/v) of the pharmaceutical composition.

12. The pharmaceutical composition of claim 6, further comprising a preservative.

13. The pharmaceutical composition of claim 12, wherein the preservative is benzalkonium chloride.

14. The pharmaceutical composition of claim 13, wherein the benzalkonium chloride is about 0.015% (w/v) of the pharmaceutical composition.

15. The pharmaceutical composition of claim 11, further comprising a preservative.

16. The pharmaceutical composition of claim 15, wherein the preservative is benzalkonium chloride.

17. The pharmaceutical composition of claim 16, wherein the benzalkonium chloride is about 0.015% (w/v) of the pharmaceutical composition.

18. The pharmaceutical composition of claim 1, comprising at least about 0.020% (w/v) to less than about 0.05% (w/v) of the dimesylate salt of (S)-4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl 2,4-dimethylbenzoate.

19. A pharmaceutical composition comprising: (a) about 0.01% (w/v) to about 1.0% (w/v) of a dimesylate salt of (S)-4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl 2,4-dimethylbenzoate; (b) boric acid; (c) mannitol; and (d) benzalkonium chloride.

20. The pharmaceutical composition of claim 19, comprising at least about 0.020% (w/v) to less than about 0.05% (w/v) of the dimesylate salt of (S)-4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl 2,4-dimethylbenzoate.

21. A pharmaceutical composition comprising: (a) about 0.01% (w/v) to about 1.0% (w/v) of a dimesylate salt of (S)-4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl 2,4-dimethylbenzoate; (b) about 0.05% (w/v) boric acid; (c) about 4.7% (w/v) D-mannitol; and (d) about 0.015% (w/v) benzalkonium chloride, wherein the pharmaceutical composition has a pH of about 5.0.

22. The pharmaceutical composition of claim 21, comprising at least about 0.020% (w/v) to less than about 0.05% (w/v) of the dimesylate salt of (S)-4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl 2,4-dimethylbenzoate.

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.