US2014066506A1PendingUtilityA1
Method for treating macular degeneration
Est. expiryApr 15, 2029(~2.8 yrs left)· nominal 20-yr term from priority
A61P 27/02A61K 2121/00A61K 31/557A61K 47/26A61K 31/5575A61K 9/0048A61K 47/14A61K 31/20
51
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Claims
Abstract
Disclosed is a method for treating macular degeneration in a mammalian subject, which includes administering to the subject in need thereof an effective amount of a 15-keto-prostaglandin compound such as 13,14-dihydro-15-keto-20-ethyl-prostaglandin F 2α isopropyl ester.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for treating macular degeneration in a mammalian subject, which comprises administering to the subject in need thereof an effective amount of a 15-keto-prostaglandin compound.
2 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a compound as shown by the following general formula (I).
wherein L, M and N are hydrogen, hydroxy, halogen, lower alkyl, hydroxy(lower)alkyl, or oxo, and the five-membered ring may have at least one double bond;
A is —CH 3 , —CH 2 OH, —COCH 2 OH, —COOH or a functional derivative thereof;
B is —CH 2 —CH 2 —, —CH═CH— or —C≡C—;
R 1 is a saturated or unsaturated bivalent lower or medium aliphatic hydrocarbon residue, which is unsubstituted or substituted with halogen, lower alkyl, hydroxy, oxo, aryl or heterocyclic group, and at least one of carbon atom in the aliphatic hydrocarbon is optionally substituted by oxygen, nitrogen or sulfur; and
Ra is a saturated or unsaturated lower or medium aliphatic hydrocarbon group, which is unsubstituted or substituted with halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or hetrocyclic-oxy group; lower alkoxy, lower aklanoyloxy, cyclo(lower)alkyl; cyclo(lower)alkyloxy; aryl; aryloxy; heterocyclic group; heterocyclic-oxy group.
3 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-prostaglandin compound.
4 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a 15-keto-20-lower alkyl-prostaglandin compound.
5 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-20-lower alkyl-prostaglandin compound.
6 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a 15-keto-20-ethyl-prostaglandin F compound.
7 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-20-ethyl-prostaglandin F compound.
8 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-20-ethyl-prostaglandin F 2α compound
9 . The method as described in claim 1 , wherein said 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-20-ethyl-prostaglandin F 2α isopropyl ester.
10 . The method as described in claim 1 , wherein said macular degeneration is age related macular degeneration.
11 . The method as described in claim 10 , wherein said age related macular degeneration is dry age related macular degeneration.
12 . The method as described in claim 1 , wherein the 15-keto-prostaglandin compound is formulated as a composition for topical administration.
13 . The method as described in claim 12 , wherein said composition is an ophthalmic composition for ocular topical administration.
14 . The method as described in claim 13 , wherein said ophthalmic composition is formulated as eye drop.
15 . The method as described in claim 14 , wherein said eye drop is formulated as a sterile unit dose type eye drop containing no preservatives.
16 . The method as described in claim 13 , wherein said ophthalmic composition comprises substantially no benzalkonium chloride.Cited by (0)
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