IP Library › Granted Patent US 10,597,394
Granted Patent B2
US 10,597,394 · App. 16/054,728 · Granted Mar 24, 2020

Organic compounds

Inventors: Sharon Mates (New York, NY); Peng Li (New Milford, NJ); Lawrence P. Wennogle (Hillsborough, NJ); Robert Davis (San Diego, CA)
Assignee: INTRA-CELLULAR THERAPIES, INC.
C07D471/16A61K31/4985A61K45/06A61P25/18A61P25/22A61P25/24C07B59/002C07D471/14
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Quick Facts
Patent No.
US 10,597,394
App. No.
16/054,728
Granted
Mar 24, 2020
Kind
B2
Abstract

This invention relates to particular substituted heterocycle fused gamma-carbolines, their prodrugs, in free, solid, pharmaceutically acceptable salt and/or substantially pure form as described herein, pharmaceutical compositions thereof, and methods of use in the treatment of diseases involving 5-HT 2A receptor, serotonin transporter (SERT) and/or pathways involving dopamine D 1 /D 2 receptor signaling systems, and/or the treatment of residual symptoms.

Claims (20)

1. A method for the treatment of a central nervous system disorder selected from anxiety, depression, psychosis, schizophrenia, post-traumatic stress disorder, impulse control disorders and intermittent explosive disorder, comprising administering to a patient in need thereof a therapeutically effective amount of compound of formula I:

wherein:

R 1 is CH 3 ;

R 2 and R 3 are each independently H or D;

R 4 and R 5 are each H;

provided that R 2 and R 3 are not both H,

and wherein D is deuterium;

in free or salt form.

2. The method according to claim 1 , wherein R 2 and R 3 are both D.

3. The method according to claim 1 , wherein R 2 is D and R 3 is H.

4. The method according to claim 1 , wherein said compound is in salt form.

5. The method according to claim 4 , wherein the salt is a toluenesulfonic acid addition salt.

6. The method according to claim 1 , wherein the method comprises administering the compound of Formula I as a pharmaceutical composition comprising the compound in free or pharmaceutically acceptable salt form, in combination or association with a pharmaceutically acceptable diluent or carrier.

7. The method according to claim 1 , wherein said disorder is selected from a group consisting of anxiety, depression, psychosis, and schizophrenia.

8. The method according to claim 7 , wherein said disorder is schizophrenia.

9. The method according to claim 7 , wherein said disorder is anxiety.

10. The method according to claim 8 , wherein the patient is suffering from residual symptoms of schizophrenia.

11. The method according to claim 10 , wherein said residual phase symptoms are selected from negative symptoms such as blunted affect, emotional withdrawal, poor rapport, passive or apathetic social withdrawal, difficulty in abstract thinking, lack of spontaneity and flow of conversation and stereotyped thinking; general psychopathology symptoms such as somatic concern, anxiety, guilt feelings, tension, mannerisms and posturing, depression, motor retardation, uncooperativeness, unusual thought content, disorientation, poor attention, lack of judgment and insight, disturbance of volition, poor impulse control, preoccupation and active social avoidance; cognitive impairment and sleep disorders.

12. The method according to claim 1 , wherein said disorder is depression.

13. The method according to claim 12 , wherein said depression is bipolar disorder.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2023
From: MATES, SHARON; LI, PENG; WENNOGLE, LAWRENCE P.; DAVIS, ROBERT E.
To: INTRA-CELLULAR THERAPIES, INC.
Reel/Frame 062943/0479 →
Continuity (3)
Continuation 15301912
Provisional Application 61975610 · Apr 4, 2014
Related Publication 20190062334A1 · Feb 28, 2019
Cited By (18)
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