IP Library › Granted Patent US 8,791,138
Granted Patent B2
US 8,791,138 · App. 12/863,513 · Granted Jul 29, 2014

Compositions and methods for alleviating depression or improving cognition

Inventors: Philip Seeman (Toronto, CA); Philip M. Tokeikis (Vancouver, CA)
Assignee: Clera Inc.
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Quick Facts
Patent No.
US 8,791,138
App. No.
12/863,513
Granted
Jul 29, 2014
Kind
B2
Abstract

This application describes compositions of receptor inhibitors, including antipsychotic agents, for example haloperidol, and methods of use for alleviating clinical depression, improving cognition and/or treating other syndromes, conditions or diseases for which anti-depressant agents are prescribed. Furthermore, this application describes compositions and methods to induce supersensitivity in dopamine D2 and other receptors involved in depression and/or cognition as a means of alleviating clinical depression or improving cognition.

Claims (10)

1. A method of treating depression comprising administering, to a subject in need thereof, an amount of haloperidol that is effective to elevate amounts of the high affinity state of the dopamine D2 receptor, inducing receptor supersensitivity, wherein the haloperidol is administered orally at a dosage of 0.05 mg to 0.5 mg each day for 3, 4, 5, 6, 7, 8, 9 or 10 consecutive days.

2. The method according to claim 1 , further comprising stopping administration of the haloperidol after receptor supersensitivity is induced, followed by restarting administration of the haloperidol after a time sufficient for receptor supersensitivity to decrease and, optionally, repeating the stopping and restarting administration cycle for a period of time effective to treat the depression.

3. The method according to claim 2 , comprising

(a) 3, 4, 5, 6, 7, 8, 9 or 10 days dosing with the haloperidol followed by 1, 2, 3, 4, 5, 6, 7, 8, 9 or 1 days of dosing with placebo;

(b) 6, 7, 8, 9 or 10 days dosing with the haloperidol followed by 6, 7, 8, 9 or 10 days of dosing with placebo; or

(c) 7, 8 or 9 days dosing with the haloperidol followed by 7, 8 or 9 days of dosing with placebo; and

(d) optionally repeating (a), (b) or (c) for a period of time effective to treat the depression.

4. The method according to claim 1 , wherein D2 receptor occupancy after administering the amount of the haloperidol that is effective to elevate dopamine D2 High receptor amounts, inducing dopamine supersensitivity, is about 2%-10%, 11%-15%, 16%-20% or 20%-25%.

5. The method according to claim 1 , wherein the haloperidol is administered for 7 days as follows: 0.2 mg on day 1, 0.2 mg on day 2, 0.25 mg on day 3, 0.25mg on day 4, 0.25 mg on day 5, 0.3 mg on day 6 and 0.3 mg on day 7 , followed by a complete cessation of the medication until a repeat treatment is clinically indicated.

6. The method according to claim 1 , wherein 0.25 mg of haloperidol is administered for 7 days followed by a complete cessation of haloperidol until a repeat treatment is clinically indicated.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2010
From: SEEMAN, PHILIP; TOLEIKIS, PHILIP
To: CLERA INC.
Reel/Frame 025097/0602 →
Continuity (2)
Provisional Application 61026279 · Feb 5, 2008
Related Publication 20100298382A1 · Nov 25, 2010