US2008306113A1PendingUtilityA1
Methods for treating macular degeneration using 4-(amino)-2-(2,6-dioxo(3-piperidyle))-isoindoline-1,3-dione
Est. expiryNov 30, 2020(expired)· nominal 20-yr term from priority
Inventors:Anthony TrestonJamshed H. ShahRobert D'AmatoKimberly A. HunsuckerJohn RougasBarry P. ConnerVictor PribdulaGlenn Swartz
A61P 3/10A61P 31/12A61P 31/22A61P 7/06A61P 5/00A61P 35/02A61P 37/02A61P 33/00A61P 35/00A61P 9/10A61P 9/00A61P 7/00A61P 35/04A61P 27/02A61P 31/10A61P 31/04A61P 25/00A61P 27/10A61P 3/02A61P 29/00A61P 27/06A61P 19/04A61P 17/02A61P 13/08A61P 19/02A61P 17/06A61P 15/00A61P 1/18A61P 1/16A61P 19/06A61P 17/00C07D 401/04A61K 31/454Y02A50/30
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Claims
Abstract
Methods of treating, preventing and/or managing macular degeneration are disclosed. Specific embodiments encompass the administration of 4-(amino)-2-(2,6-dioxo(3-piperidyl))-isoindoline-1,3-dione, or a pharmaceutically acceptable salt, solvate or stereoisomer thereof, alone or in combination with a second active agent and/or surgery.
Claims
exact text as granted — not AI-modified1 - 16 . (canceled)
17 . A method of treating macular degeneration, which comprises administering to a patient having macular degeneration a therapeutically effective amount of 4-(amino)-2-(2,6-dioxo(3-piperidyl))-isoindoline-1,3-dione of the formula:
or an enantiomer thereof.
18 . The method of claim 17 , wherein the compound is 4-(amino)-2-(2,6-dioxo(3-piperidyl))-isoindoline-1,3-dione.
19 . The method of claim 17 , wherein the enantiomer is an enantiomerically pure R isomer.
20 . The method of claim 17 , wherein the enantiomer is an enantiomerically pure S isomer.
21 . The method of claim 17 , wherein the compound is administered orally.
22 . The method of claim 21 , wherein the compound is administered in the form of a capsule or tablet.
23 . The method of claim 17 , wherein the compound is administered in an amount of from about 0.1 to about 300 mg/kg per day.
24 . The method of claim 23 , wherein the compound is administered in an amount of from about 0.5 to about 50 mg/kg per day.
25 . The method of claim 23 , wherein the compound is administered in an amount of from about 0.1 to about 2 mg/kg per day.
26 . The method of claim 17 , wherein the compound is administered orally, opthalmically, parenterally, transdermally, mucosally, nasally, buccally, rectally, sublingually, topically or vaginally.
27 . The method of claim 17 , wherein the compound is administered in the form of a cream, a lotion, an ointment, a patch, a gel, a paste, a liquid, a solution, an emulsion, a suspension, a dispersion, a spray, or a drop.Cited by (0)
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