IP Library Granted Patent US 9,174,975
Granted Patent B2
US 9,174,975 · App. 10/525,021 · Granted Nov 3, 2015

Remedy for integration dysfunction syndrome

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Quick Facts
Patent No.
US 9,174,975
App. No.
10/525,021
Granted
Nov 3, 2015
Kind
B2
Abstract

The present invention provides a novel method for treatment of schizophrenia which can improve wide-ranging symptoms of schizophrenia, especially positive symptoms and negative symptoms without being accompanied by extrapyramidal symptoms, which comprises orally administering as an active compound (1R,2S,3R,4S)—N-[(1R,2R)-2-[4-(1,2-benzoisothiazol-3-yl)-1-piperazinylmethyl]-1-cyclohexylmethyl]-2,3-bicyclo[2.2.1]heptanedicarboxyimide or a pharmaceutically acceptable salt thereof (e.g., hydrochloride) at a daily dose of 5 mg to 120 mg once a day to a patient with schizophrenia, and a therapeutic agent to be used in the method.

Claims (12)

1. A method for treating the negative symptoms of schizophrenia and/or the cognitive dysfunction of schizophrenia in a patient, which comprises orally administering a once daily dose of 5 mg to 120 mg of the active compound: (1R,2S,3R,4S)—N[(1R,2R)-2-[4-(1,2-benzoisothiazol-3-yl)-1-piperazinylmethyl]-1-cyclohexylmethyl]-2,3-bicyclo[2.2.1]heptanedicarboxyimide of the formula (1):

or a pharmaceutically acceptable salt thereof to a patient suffering from negative symptoms of schizophrenia and/or cognitive dysfunction of schizophrenia.

2. The method of claim 1 , which is a method for treating the negative symptoms of schizophrenia in a patient.

3. The method of claim 1 , which is a method for treating the cognitive dysfunction of schizophrenia in a patient.

4. The method of claim 1 , 2 or 3 wherein the pharmaceutically acceptable salt of said active compound is (1R,2S,3R,4S)—N-[(1R,2R)-2-[4-(1,2benzoisothiazol-3-yl)-1-piperazinylmethyl]-1-cyclohexylmethyl]-2,3-bicyclo[2.2.1]heptanedicarboxyimide hydrochloride.

5. The method of any one of claims 1 , 4 , 2 and 3 , wherein a once daily dose of 20 mg to 80 mg of said active compound or a pharmaceutically acceptable salt thereof is administered to said patient.

6. The method of any one of claims 1 , 4 , 2 and 3 , wherein said patient is in a chronic stage of schizophrenia, and wherein a once daily dose of 5 mg to 80 mg of said active compound or a pharmaceutically acceptable salt thereof is administered to said patient.

7. The method of any one of claims 1 , 4 , 2 and 3 , wherein said patient is in an acute stage of schizophrenia, and wherein a once daily dose of 40 mg to 120 mg of said active compound or a pharmaceutically acceptable salt thereof is administered to said patient.

8. The method of any one of claims 1 , 4 , 2 and 3 , wherein a once daily dose of 40 mg of said active compound or a pharmaceutically acceptable salt thereof is administered to said patient.

9. The method of any one of claims 1 , 4 , 2 and 3 , wherein a once daily dose of 80 mg of said active compound or a pharmaceutically acceptable salt thereof is administered to said patient.

10. The method of any one of claims 1 , 4 , 2 and 3 , wherein a once daily dose of 120 mg of said active compound or a pharmaceutically acceptable salt thereof is administered to said patient.

11. The method of claim 6 , wherein a once daily dose of 10 mg to 80 mg of said active compound or a pharmaceutically acceptable salt thereof is administered to said patient.

Assignments (4)
CHANGE OF NAME Recorded Nov 21, 2022
From: SUMITOMO DAINIPPON PHARMA CO., LTD.
To: SUMITOMO PHARMA CO., LTD.
Reel/Frame 061972/0730 →
CHANGE OF NAME Recorded Oct 7, 2014
From: DAINIPPON SUMITOMO PHARMA CO., LTD.
To: SUMITOMO DAINIPPON PHARMA CO., LTD.
Reel/Frame 033905/0778 →
MERGER Recorded Dec 16, 2005
From: SUMITOMO PHARMACEUTICALS COMPANY, LTD.
To: DAINIPPON SUMITOMO PHARMA CO., LTD.
Reel/Frame 017089/0420 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2005
From: NAKAMURA, MITSUTAKA; OGASA, MASAAKI; SAMI, SHUNSUKE
To: SUMITOMO PHARMACEUTICALS COMPANY LIMITED
Reel/Frame 016898/0569 →