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Last Updated: December 23, 2024

Claims for Patent: 7,727,993

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Summary for Patent: 7,727,993

Title:	Administering adenosine A.sub.2A receptor antagonist to reduce or suppress side effects of parkinson's disease therapy
Abstract:	The present invention is directed to methods of treating movement disorders by administering an effective amount of one or more adenosine A.sub.2A receptor antagonists to a patient in need thereof. The present invention also provides methods of decreasing the adverse effects of L-DOPA in patients receiving L-DOPA therapy in the treatment of Parkinson's disease. The present invention further provides methods and compositions for treating Parkinson's disease patients with sub-clinically effective doses of L-DOPA by combining L-DOPA treatment with an effective amount of one or more adenosine A.sub.2A receptor antagonists (i.e., L-DOPA sparing effect). The present invention further provides methods of effective treatment of Parkinson's disease by co-administering at least one adenosine A.sub.2A receptor antagonist, L-DOPA and a dopamine agonist and/or a COMT inhibitor and/or a MAO inhibitor. The present invention further provides methods of prolonging effective treatment of Parkinson's disease by administering an adenosine A.sub.2A receptor antagonist singly or together with a dopamine agonist, and/or a COMT inhibitor, and/or a MAO inhibitor without prior or subsequent administration of L-DOPA, delaying or removing on-set of L-DOPA motor complication.
Inventor(s):	Kase; Hiroshi (Tokyo, JP), Mori; Akihisa (Chiba, JP), Waki; Yutaka (Princeton, NJ), Ohsawa; Yutaka (London, GB), Karasawa; Akira (Shizuoka, JP), Kuwana; Yoshihisa (Shizuoka, JP)
Assignee:	Kyowa Hakko Kirin Co., Ltd. (Tokyo, JP)
Application Number:	11/326,414
Patent Claims:	1. A method of reducing or suppressing adverse effects from L-DOPA therapy, comprising administering, to a human patient with Parkinson's Disease, an effective amount of (E)-8-(3,4-dimethoxystyryl)-1,3-diethyl-7-methylxanthine or a pharmaceutically acceptable salt thereof, wherein the patient currently receives said L-DOPA therapy. 2. The method according to claim 1, wherein the patient suffers from L-DOPA-induced motor complications. 3. The method according to claim 2, wherein OFF time in motor fluctuations is reduced. 4. The method according to claim 2, wherein dyskinesias in motor complications are improved. 5. The method according to claim 1, wherein OFF time in motor fluctuations is reduced. 6. The method according to claim 1, wherein dyskinesias in motor complications are improved. 7. The method according to claim 1, wherein the adverse effect comprises ON/OFF fluctuations. 8. The method according to claim 1, wherein the adverse effect comprises wearing off phenomenon. 9. The method according to claim 1, wherein the adverse effect comprises dyskinesia. 10. The method according to claim 2, wherein the adverse effect comprises ON/OFF fluctuations. 11. The method according to claim 2, wherein the adverse effect comprises wearing off phenomenon. 12. The method according to claim 2, wherein the adverse effect comprises dyskinesia.

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