IP Library Granted Patent US 7,932,289
Granted Patent B2
US 7,932,289 · App. 11/658,450 · Granted Apr 26, 2011

Remedy for diabetes

Assignee: Takeda Pharmaceutical Company Limited
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Quick Facts
Patent No.
US 7,932,289
App. No.
11/658,450
Granted
Apr 26, 2011
Kind
B2
Abstract

The present invention relates to a therapeutic agent for diabetes with sulfonylurea secondary failure, which contains a GPR40 agonist. According to the present invention, a therapeutic agent for diabetes with sulfonylurea secondary failure that affords a superior insulin secretion effect and a superior hypoglycemic effect even in diabetic patients for whom a sulfonylurea compound or a fast-acting insulin secretagogue fails to provide an insulin secretion effect and therefore, fails to provide a sufficient hypoglycemic effect can be provided.

Claims (12)

1. A method for treating type 2 diabetes with sulfonylurea secondary failure in a mammal, which comprises administering an effective amount of a compound represented by the formula:

wherein ring P is an aromatic ring optionally having substituent(s), ring Q is an aromatic ring optionally further having substituent(s) besides —Y—COOH, and X and Y are each independently a spacer,

or a salt thereof, to the mammal.

2. The method of claim 1 , wherein the sulfonylurea secondary failure is caused by a sulfonylurea compound.

3. The method of claim 1 , wherein the sulfonylurea secondary failure is caused by a fast-acting insulin secretagogue.

4. The method of claim 1 , wherein the compound is a compound represented by the formula

wherein ring P 1 is a benzene ring having substituent(s) having a benzene ring, ring Q 1 is a benzene ring optionally having substituent(s), and R is a hydrogen atom or a substituent;

or a salt thereof.

5. The method of claim 4 , wherein

ring P 1 is a benzene ring having substituent(s) represented by the formula: R 1 -E 1 -, wherein R 1 is a phenyl group or an indanyl group, each optionally having substituent(s) selected from the group consisting of halogen atom, nitro group, carboxyl group, optionally halogenated C 1-6 alkyl group, hydroxy-C 1-6 alkyl group, carboxy-C 1-6 alkyl-carbonylamino-C 1-6 alkyl group, optionally halogenated C 1-6 alkoxy group, C 6-14 aryl group, C 6-14 aryloxy group and C 7-16 aralkyloxy group, and E 1 is a bond or a spacer selected from the group consisting of —O—, —CH 2 —O—, —CO—, —CONH—, —N(CH 3 )CH 2 —, —S—CH 2 — and —CH═CH—, and the benzene ring is optionally substituted by C 1-6 alkyl group;

ring Q 1 is a benzene ring optionally having C 1-6 alkyl group; and

R is a hydrogen atom.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2007
From: SUZUKI, NOBUHIRO; SUZUKI, MASAMI; ASAKAWA, TOMOKO; KATAOKA, OSAMU
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 018924/0678 →
Priority Claims (1)
JP 2004-218736 · Jul 27, 2004 · national
Continuity (1)
Related Publication 20080319077A1 · Dec 25, 2008