US2005009856A1PendingUtilityA1
Treatment of dyskinesia
Est. expiryJul 18, 2018(expired)· nominal 20-yr term from priority
Inventors:Jonathan Brotchie
A61P 39/00A61P 43/00A61K 48/00A61P 25/14A61P 25/02A61P 25/00A61K 31/485A61P 25/16A61P 25/30A61P 25/18A61K 31/4184A61K 31/00
52
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Claims
Abstract
The invention relates to the use of compounds which inhibit selectively mu opioid receptor activity, or activation, for the treatment of dyskinesia (which, for example, may arise as a side effect of L-DOPA therapy). The compounds used are preferably mu opioid receptor antagonists such as cyprodime.
Claims
exact text as granted — not AI-modified1 - 21 . (Cancel).
22 . A method for the treatment of dyskinesia comprising administering to a person or animal in need of said treatment an amount of a compound which inhibits selectively mu opioid receptor activity or activation sufficient to effect said treatment.
23 . The method according to claim 22 wherein said dyskinesia is associated with movement disorders.
24 . The method according to claim 23 , wherein said dyskinesia is associated with parkinsonism.
25 . The method according to claim 24 wherein the parkinsonism is idiopathic Parkinson's disease or post-encephalitic parkinsonism.
26 . The method according to claim 24 wherein the parkinsonism results from head injury, the treatment of schizophrenia, drug intoxication or manganese poisoning.
27 . The method according to claim 22 wherein said dyskinesia is associated with Huntington's disease, idiopathic torsion dystonia, tardive dyskinesia or off-dystonia in Parkinson's disease, the treatment of schizophrenia, drug intoxication or manganese poisoning.
28 . The method according to claim 22 wherein said dyskinesia arises as a side-effect of a therapeutic agent.
29 . The method according to claim 28 , wherein said dyskinesia is associated with agents used to treat movement disorders.
30 . The method according to claim 22 , wherein the compound is a mu opioid receptor antagonist.
31 . The method according to claim 22 , wherein said amount is between 0.1 mgs/kg/day and 500 mgs/kg/day.
32 . The method according to claim 22 , wherein said amount is between 0.3 mgs/kg/day and 100 mgs/kg/day.
33 . The method according to claim 22 , wherein said amount is about 10 mgs/kg/day.
34 . The method according to claim 22 , wherein said compound is present in a composition in the form of a powder, tablet, capsule, liquid, ointment, cream, gel, hydrogel, aerosol, spray, micelle, or liposome.
35 . The method according to claim 22 wherein the composition is in a form suitable for oral administration.
36 . The method according to claim 22 wherein said treatment is prophylactic treatment.Join the waitlist — get patent alerts
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