US2008064724A1PendingUtilityA1
Composition Comprising Methylphenidate and Another Drug
Est. expiryJul 14, 2015(expired)· nominal 20-yr term from priority
A61K 33/00A61K 31/4458A61K 45/06A61P 25/00A61K 31/445
70
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Claims
Abstract
A process of treating a subject that is undergoing methylphenidate therapy and concomitant therapy with another drug undergoes or interferes with P 450 metabolism wherein the methylphenidate is d-threo-methylphenidate.
Claims
exact text as granted — not AI-modified1 . A method of treating a subject that is undergoing methylphenidate therapy and concomitant therapy with another drug, wherein said therapy is for attention-deficit hyperactivity disorder and said method provides for reduced side effects or reduced potential for abuse relative to racemic methylphenidate, said method comprising administering an effective amount of d-threo-methylphenidate to said subject daily.
2 . The method according to claim 1 , wherein said d-threo-methylphenidate and said another drug is formulated for administration to an adult patient.
3 . The method according to claim 1 , wherein the dosage of d-threo-methylphenidate administered to said subject is 5 mg to 60 mg.
4 . The method according to claim 1 , wherein said d-threo-methylphenidate is in at least 95% enantiomeric excess relative to l-threo-methylphenidate.
5 . A method for treating a patient having a condition susceptible to treatment with methylphenidate and also exhibiting or likely to exhibit other central nervous system disorders, wherein said condition is attention-deficit disorder or attention-deficit hyperactivity disorder and said method provides for reduced side effects or reduced potential for abuse relative to racemic methylphenidate, said method comprising administering an effective amount of d-threo-methylphenidate to said patient daily.
6 . The method according to claim 5 , wherein the dosage of d-threo-methylphenidate administered to said patient is 5 mg to 60 mg.
7 . The method according to claim 5 , wherein said d-threo-methylphenidate is in at least 95% enantiomeric excess relative to l-threo-methylphenidate.
8 . A method for treating a patient having a condition that is susceptible to treatment with methylphenidate and concomitant therapy with another drug, wherein said condition is attention-deficit disorder or attention-deficit hyperactivity disorder and said method provides for reduced side effects or reduced potential for abuse relative to racemic methylphenidate, said method comprising administering an effective amount of d-threo-methylphenidate to said patient daily.
9 . The method according to claim 8 , wherein the dosage of d-threo-methylphenidate administered to said patient is 5 mg to 60 mg.
10 . The method according to claim 8 , wherein said d-threo-methylphenidate is in at least 95% eneantiomeric excess relative to --threo-methylphenidate.Join the waitlist — get patent alerts
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