USRE39609EExpiredUtility
8-iso-prostaglandins for glaucoma therapy
Est. expiryMay 9, 2017(expired)· nominal 20-yr term from priority
A61K 31/5575A61P 27/06
55
PatentIndex Score
0
Cited by
16
References
24
Claims
Abstract
The present invention relates to the use of 8-iso prostaglandins and their derivatives for decreasing intraocular pressure, for example in the treatment of glaucoma It is based, at least in part, on the discovery that 8-iso prostaglandin E 2 effectively decreased intraocular pressure by a trabecular meshwork outflow mechanism.
Claims
exact text as granted — not AI-modified1. A method for decreasing intraocular pressure comprising administering a therapeutically effective amount of an 8-iso prostanoid having the following Formula I:
where bond W is selected from the group consisting of a single covalent bond and a double covalent bond, bond X is selected from the group consisting of a single covalent bond and a double bond, substituent Y is selected from the group consisting of a hydroxyl group having either α or β orientation relative to the five-membered ring and a keto function, and substituent Z is a hydrocarbon group selected from the group of aliphatic, aromatic, or a combination of aliphatic and aromatic hydrocarbon, to a patient in need of such treatment.
2. The method of claim 1 wherein the 8-isoprostanoid is administered topically.
3. The method of claim 2 wherein the 8-iso prostanoid is administered as a composition comprising between 0.005 to 1 percent 8-iso prostanoid.
4. The method of claim 1 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula II
or a derivative thereof.
5. The method of claim 1 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula III
or a derivative thereof.
6. The method of claim 1 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula IV
or a derivative thereof.
7. The method of claim 2 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula II
or a derivative thereof.
8. The method of claim 2 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula III
or a derivative thereof.
9. The method of claim 2 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula IV
or a derivative thereof.
10. The method of claim 3 , wherein 8-iso prostanoid is selected from the group consisting of a compound having the following Formula II
or a derivative thereof.
11. The method of claim 3 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula III
or a derivative thereof.
12. The method of claim 3 , wherein the 8-iso prostanoid is selected from the group consisting of a compound having the following Formula IV
or a derivative thereof.
13. The method of claim 4 , wherein the derivative is an ester derivative.
14. The method of claim 5 , wherein the derivative is an ester derivative.
15. The method of claim 6 , wherein the derivative is an ester derivative.
16. The method of claim 7 , wherein the derivative is an ester derivative.
17. The method of claim 8 , wherein the derivative is an ester derivative.
18. The method of claim 9 , wherein the derivative is an ester derivative.
19. The method of claim 10 , wherein the derivative is an ester derivative.
20. The method of claim 11 , wherein the derivative is an ester derivative.
21. The method of claim 12 , wherein the derivative is an ester derivative.
22. A method for decreasing intraocular pressure comprising administering a therapeutically effective amount of an 8 - iso prostanoid having the following Formula I:
where bond W is selected from the group consisting of a single covalent bond and a double covalent bond, bond X is selected from the group consisting of a single covalent bond and a double covalent bond and substituent Y is selected from the group consisting of a hydroxyl group having either α or β orientation relative to the five - membered ring and a keto function, to a patient in need of such treatment.
23. The method of claim 22 wherein the 8 - iso prostanoid is administered topically.
24. The method of claim 22 wherein the 8 - iso prostanoid is administered as a composition comprising between 0 . 005 to 1 percent 8 - iso prostanoid.Cited by (0)
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