US2021196654A1PendingUtilityA1
Method of treating conditions
Est. expiryDec 30, 2039(~13.4 yrs left)· nominal 20-yr term from priority
A61K 9/16A61K 9/141A61K 9/2054A61K 31/381A61K 31/138A61K 31/15A61P 25/18A61K 31/343A61P 25/24A61K 31/135A61K 31/4525A61K 31/137A61K 9/0053A61P 25/28A61P 25/22A61P 25/02A61K 45/06
60
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Claims
Abstract
The present invention provides a method for safe and efficacious administration of esketamine.
Claims
exact text as granted — not AI-modifiedWhat is claimed:
1 . A method of treating bipolar disorder in a human patient in need thereof comprising orally administering to said patient an oral dosage form comprising between about 5 mg and about 40 mg of esketamine over a treatment regimen of at least 28 days.
2 . The method of claim 1 , wherein the bipolar disorder is selected from the group consisting of bipolar I disorder, bipolar II disorder and cyclothymic disorder.
3 . The method of claim 1 , wherein the oral dosage form comprises about 40 mg of esketamine.
4 . The method of claim 1 , wherein the treatment regimen is between 28 days and about 730 days.
5 . The method of claim 1 , wherein the treatment regimen results in a reduction of the symptoms of bipolar disorder after at least 28 days of treatment.
6 . The method of claim 1 , wherein the administration is at least once daily over the treatment regimen.
7 . The method of claim 6 , wherein the administration is once daily over the treatment regimen.
8 . The method of claim 1 , wherein the administration is intermittent over the treatment regimen.
9 . The method of claim 8 , wherein the administration is once every second day to once a month of the treatment regimen.
10 . The administration of claim 8 , wherein the frequency of the administration varies over the treatment regimen.
11 . The method of claim 1 , further comprising the administration of a second medication other than (R)-ketamine.
12 . The method of claim 11 , wherein the second medication is an antidepressant or an antimanic agent.
13 . The method of claim 12 , wherein the antidepressant is selected from the group consisting of fluoxetine, sertraline, paroxetine, citalopram, escitalopram, venlafaxine, desvenlafaxine, duloxetine, and fluvoxamine.
14 . The method of claim 1 , wherein the esketamine C max of said administration is 30 ng/ml or less.
15 . The method of claim 1 , wherein the esketamine AUC 0-t of said administration is 60 ng*h/ml or less.
16 . The method of claim 1 , wherein the esketamine C max of said administration is 30 ng/ml or less and the esketamine AUC 0-t of said administration is 60 ng*h/ml or less.
17 . The method of claim 16 , wherein the esketamine C max of said administration is 15 ng/ml or less and the esketamine AUC 0-t of said administration is 30 ng*h/ml or less.
18 . The method of claim 1 , wherein the esketamine is esketamine hydrochloride.
19 . A method of treating bipolar disorder in a human patient in need thereof comprising orally administering to said patient a dosage form, wherein said dosage form provides for an esketamine C max of 30 ng*h/ml or less.
20 . A method of treating bipolar disorder in a human patient in need thereof comprising orally administering to said patient a dosage form, wherein said dosage form provides for an esketamine AUC 0-t of 850 ng*h/ml or less.Join the waitlist — get patent alerts
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