Bupropion as a modulator of drug activity
AssigneeAntecip Bioventures II LLC
InventorHerriot Tabuteau
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Abstract
Disclosed herein are methods of treating neurological or psychiatric diseases or disorders using a combination of bupropion and dextromethorphan. Related compositions and dosage forms are also described.
Claims19
A method of treating major depressive disorder, comprising administering a dosage form by mouth once daily for three days followed by twice daily by mouth to a human patient in need thereof for a total of at least 8 days, wherein the dosage form comprises about 105 mg of bupropion hydrochloride and about 45 mg of a dextromethorphan salt as the only therapeutically active compounds in the dosage form, wherein on the eighth day that the dosage form is administered, the Cmax of bupropion in the human patient is about 9×101 ng/mL, wherein the human patient does not experience an adverse event as a result of receiving the dosage form, and wherein the adverse event is dizziness.
A method of treating major depressive disorder, comprising administering a dosage form by mouth once daily for three days followed by twice daily by mouth to a human patient in need thereof for a total of at least 8 days, wherein the dosage form consists essentially of about 105 mg of bupropion hydrochloride and about 45 mg of a dextromethorphan salt, wherein the human patient does not experience an adverse event as a result of receiving the dosage form, wherein on the eighth day that the dosage form is administered, the Cmax of bupropion in the human patient is about 9×101 ng/mL, and wherein the adverse event is dizziness.
A method of treating major depressive disorder, comprising orally administering a dosage form once daily by mouth for three days followed by twice daily by mouth to a human patient in need thereof, for a total of at least 8 days wherein the therapeutically active compounds in the dosage form consist of (i) about 105 mg of bupropion hydrochloride and (ii) about 45 mg of a dextromethorphan salt, wherein the human patient does not experience an adverse event as a result of receiving the dosage form, wherein on the eighth day that the dosage form is administered, the Cmax of bupropion in the human patient is about 9×101 ng/mL, and wherein the adverse event is dizziness.
Dependencies are inferred from the claim text.