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US Patent 11439629 Methods for the administration of certain VMAT2 inhibitors

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Contents

Is a
Patent
Patent

Patent attributes

Patent Applicant
Neurocrine Biosciences
Neurocrine Biosciences
Current Assignee
Neurocrine Biosciences
Neurocrine Biosciences
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
11439629
Date of Patent
September 13, 2022
Patent Application Number
17080343
Date Filed
October 26, 2020
Patent Citations
‌
US Patent 10874648 Methods for the administration of certain VMAT2 inhibitors
‌
US Patent 10906902 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-2-amino-3-methylbutanoate di(4-methylbenzenesulfonate)
‌
US Patent 10906903 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1,-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate)
‌
US Patent 10912771 Methods for the administration of certain VMAT2 inhibitors
‌
US Patent 10919892 Synthetic methods for preparation of (S)-(2R,3R,11bR)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate)
‌
US Patent 10952997 Methods for the administration of certain VMAT2 inhibitors
‌
US Patent 10993941 Methods for the administration of certain VMAT2 inhibitors
‌
US Patent 11026939 High dosage valbenazine formulation and compositions, methods, and kits related thereto
...
Patent Citations Received
‌
US Patent 11654142 Methods for the administration of certain VMAT2 inhibitors
0
Patent Primary Examiner
‌
Umamaheswari Ramachandran
CPC Code
‌
A61K 31/4709
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A61K 31/4745
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A61K 31/495
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A61K 9/0053
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A61K 9/48
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A61P 1/16
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A61P 25/14
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C07D 455/06
...

Provided are methods of administering a vesicular monoamine transport 2 (VMAT2) inhibitor chosen from valbenazine and (+)-α-3-isobutyl-9,10-dimethoxy-1, 3,4, 6,7,11 b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-ol, or a pharmaceutically acceptable salt and/or isotopic variant thereof, to a patient in need thereof wherein the patient is a CYP2D6 poor metabolizer.

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