IP Library Granted Patent US 8,193,172
Granted Patent B2
US 8,193,172 · App. 10/496,222 · Granted Jun 5, 2012

Methods for the treatment of major depressive disorder using glucocorticoid receptor antagonists

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Quick Facts
Patent No.
US 8,193,172
App. No.
10/496,222
Granted
Jun 5, 2012
Kind
B2
Abstract

The present invention relates to a method for the treatment of a patient suffering from major depressive disorder by administering to the patient an effective amount of a glucocorticoid receptor antagonist and to methods for establishing the optimal treatment regimen.

Claims (4)

1. A method for treatment with the compound (11β, 17β)-11-(1,3-benzodioxol-5-yl)-17-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one of a patient suffering from major depressive disorder by determining, prior to treatment, a peripheral cortisol level at a selected time of day, then measuring peripheral cortisol level, at the selected time of day, after administering at least one daily dose of the compound to the patient, and continuing administration of the compound with a daily dose which, on the basis of corresponding daily measurements of peripheral cortisol level, is determined to be the highest daily dose that does not increase the peripheral cortisol level beyond the peripheral cortisol level measured prior to treatment.

2. The method of claim 1 wherein the selected time of day is in the afternoon.

3. A method for treatment with the compound (11β,17β)-11-(1,3-benzodioxol-5-yl)-17-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one of a patient suffering from major depressive disorder by determining, prior to treatment, a peripheral cortisol level at a selected time of day, then measuring peripheral cortisol level, at the selected time of day, after administering at least one daily dose of the compound to the patient, and continuing administration of the compound with a daily dose selected from the list consisting of 25 mg, 150 mg, 300 mg, 450 mg, 600 mg, 750 mg and 900 mg by selecting the amount in the list immediately below that which, on the basis of corresponding daily measurements of peripheral cortisol level, is determined to be the highest daily dose that does not increase the peripheral cortisol level beyond the peripheral cortisol level measured prior to treatment.

4. The method of claim 3 wherein the selected time of day is in the afternoon.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2011
From: N.V. ORGANON
To: POP TEST CORTISOL LLC
Reel/Frame 026096/0714 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2007
From: AKZO NOBEL N.V.
To: N.V. ORGANON
Reel/Frame 018816/0737 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2004
From: SENNEF, CORNELIS; PEETERS, BERNARDUS W. M.M.
To: AKZO NOBEL N.V.
Reel/Frame 015110/0710 →