US2006030587A1PendingUtilityA1
Method of treating attention deficit disorders with d-threo methylphenidate
Est. expiryDec 4, 2015(expired)· nominal 20-yr term from priority
A61K 9/1676A61K 31/445A61K 9/2886C12P 41/006A61K 9/5084A61P 25/28C12P 17/12A61K 9/5078A61P 25/00A61K 31/4458C07D 211/34
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Claims
Abstract
Methods for treating Attention Deficit Disorder, Attention Deficit Hyperactivity Disorder, AIDS Dementia Complex and cognitive decline in HIV-AIDS while minimizing drug hypersensitivity, toxicity, side effects, euphoric effect, and drug abuse potential by administration of d-threo-methylphenidate or pharmaceutically acceptable salts thereof.
Claims
exact text as granted — not AI-modified1 . A method of treating Attention Deficit Disorder on a daily basis while reducing side effects associated with the administration of racemic threo methylphenidate which comprises administrating on a daily basis to a human in need thereof an amount of D-threo methylphenidate or a pharmaceutically acceptable salt thereof, substantially free of L-threo methylphenidate, wherein the amount administered is effective to treat Attention Deficit Disorder while reducing side effects associated with racemic threo methylphenidate.
2 . The method according to claim 1 wherein the amount administered is 5 mg to 50 mg per day.
3 . The method according to claim 2 wherein the amount administered is 5 mg per day.
4 . The method according to claim 1 wherein the amount of said d-threo methylphenidate or a pharmaceutically equivalent salt thereof is greater than 90% of the total amount of methylphenidate.
5 . The method according to claim 4 wherein the amount of said d-threo methylphenidate or a pharmaceutically equivalent salt thereof is greater than 99% of the total amount of methylphenidate.
6 . The method according to claim 1 wherein the side effects are anorexia, weight loss, insomnia, dizziness, or dysphoria.
7 . The method according to claim 1 wherein the side effect is a euphoric effect.
8 . The method according to claim 1 wherein the side effect is drug abuse potential.
9 . The method according to claim 1 wherein the amount of D-threo methylphenidate enhances therapeutic activity compared to racemic methylphenidate.
10 . The method according to claim 1 wherein the administration is daily.
11 . The method according to claim 1 wherein the administration is one to four times per day.
12 . The method according to claim 1 wherein said amount of D-threo methylphenidate or pharmaceutically acceptable salt thereof comprises a carrier or diluent.Join the waitlist — get patent alerts
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