IP Library › Granted Patent US 8,754,032
Granted Patent B2
US 8,754,032 · App. 11/916,356 · Granted Jun 17, 2014

Concomitant pharmaceutical agents and use thereof

Inventors: Yuji Abe (Osaka, JP); Jun Anabuki (Osaka, JP); Fumihiko Akahoshi (Osaka, JP)
Assignee: Mitsubishi Tanabe Pharma Corporation
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Quick Facts
Patent No.
US 8,754,032
App. No.
11/916,356
Granted
Jun 17, 2014
Kind
B2
Abstract

A concomitant agent to be used simultaneously or separately, comprising a combination of (a) 3-{(2S,4S)-4-[4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl]pyrrolidin-2-ylcarbonyl}thiazolidine, a salt of the compound with an organic or inorganic and mono- or di-basic acid or a solvate thereof, and (b) at least one kind of active ingredient selected from the group consisting of an active ingredient of a pharmaceutical agent selected from (i) an antidiabetic drug, (ii) a lipid lowering drug, (iii) an antihypertensive drug, (iv) a therapeutic drug for diabetic complications, (v) an antiobesity drug, (vi) an antiplatelet drug and (vii) an anticoagulant, a pharmaceutically acceptable salt thereof and a solvate thereof.

Claims (12)

1. A method for treating hyperglycemia, diabetes, an insulin resistant glucose metabolism disorder, an impaired glucose tolerance condition, or an impaired fasting plasma glucose condition in a warm-blooded mammal, which comprises simultaneously or separately administering

(a) 1-50 mg of 3-{(2S,4S)-4-[4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl]pyrrolidin-2-ylcarbonyl}thiazolidine 2.5 hydrobromide, or a hydrate thereof, and

(b) an antidiabetic drug selected from the group consisting of (i) a sulfonylurea agent, (ii) a glitazone, (iii) a biguanide, and (iv) an alpha-glucosidase inhibitor, or a pharmaceutically acceptable salt thereof,

to a warm-blooded mammal, thereby treating hyperglycemia, diabetes, an insulin resistant glucose metabolism disorder, an impaired glucose tolerance condition, or an impaired fasting plasma glucose condition in the warm-blooded mammal.

2. The method of claim 1 , wherein the antidiabetic drug is at least one agent selected from the group consisting of metformin and an α-glucosidase inhibitor, and pharmaceutically acceptable salts thereof.

3. The method of claim 1 , wherein the antidiabetic drug is selected from the group consisting of glimepiride, glipizide, and glyburide, or a pharmaceutically acceptable salt thereof.

4. The method of claim 1 , wherein the antidiabetic drug is selected from the group consisting of pioglitazone, troglitazone, and rosiglitazone, or a pharmaceutically acceptable salt thereof.

5. The method of claim 1 , wherein the antidiabetic drug is metformin or a pharmaceutically acceptable salt thereof.

6. The method of claim 1 , wherein the antidiabetic drug is selected from the group consisting of acarbose, voglibose, and miglitol, or a pharmaceutically acceptable salt thereof.

7. A method of decreasing plasma glucose level in a warm-blooded mammal without causing insulin secretion, which comprises simultaneously or separately administering

(a) 1-50 mg of 3-{(2S,4S)-4-[4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl]pyrrolidin-2-ylcarbonyl}thiazolidine 2.5 hydrobromide, or a hydrate thereof, and

(b) an alpha-glucosidase inhibitor or a pharmaceutically acceptable salt thereof, to a warm-blooded mammal, thereby decreasing the plasma glucose level in the warm-blooded mammal.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE INDICATED DATE OF EXECUTION OF THE SECOND ASSIGNOR PREVIOUSLY RECORDED ON REEL 020598 FRAME 0051. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 18, 2008
From: ABE, YUJI; ANABUKI, JUN; AKAHOSHI, FUMIHIKO
To: MITSUBISHI TANABE PHARMA CORPORATION
Reel/Frame 021111/0799 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2008
From: ABE, YUJI; ANABUKI, JUN; AKAHOSHI, FUMIHIKO
To: MITSUBISHI TANABE PHARMA CORPORATION
Reel/Frame 020598/0051 →
Priority Claims (1)
JP 2005-164213 · Jun 3, 2005 · national
Continuity (1)
Related Publication 20090082256A1 · Mar 26, 2009