IP Library Granted Patent US 8,889,660
Granted Patent B2
US 8,889,660 · App. 13/679,592 · Granted Nov 18, 2014

Methods for treating obesity or an obesity related condition

Inventors: Krzysztof Palczewski (Bay Village, OH); Radu Moise (Cleveland, OH)
Assignee: Case Western Reserve University
A61K31/07A61K31/203A61K31/215Y10S514/909
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Quick Facts
Patent No.
US 8,889,660
App. No.
13/679,592
Granted
Nov 18, 2014
Kind
B2
Abstract

In one aspect of the present invention, a pharmaceutical composition for treating a metabolic disease in a mammalian subject includes a therapeutically effective amount of (R)-all-trans-13,14-dihydroretinol and a pharmaceutically acceptable carrier or diluent. In another aspect of the present invention, pharmaceutical composition for treating a metabolic disease in a mammalian subject includes a therapeutically effective amount of (S)-all-trans-13,14-dihydroretinol and a pharmaceutically acceptable carrier or diluent. In a further aspect of the present invention, a method is provided for treating a metabolic disease in a mammalian subject. The method includes administering to the subject a pharmaceutical composition comprising at least one all-trans-13,14-dihydroretinoid, all-trans-13,14-dihydroretinoid derivative, or agent capable of modulating the level of at least one all-trans-13,14-dihydroretinoid or all-trans-13,14-dihydroretinoid derivative in the subject.

Claims (7)

1. A method of treating obesity or an obesity related condition in a mammalian subject, the method comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising at least one all-trans-13,14-dihydroretinoid, all-trans-13,14-dihydroretinoid derivative, or all-trans-retinol: all-trans-13,14-dihydroretinol saturase, wherein the obesity or obesity related condition is associated with improved glucose tolerance, abnormal fasting response manifested by visceral fat retention, or decreased hepatic triglyceride levels.

2. The method of claim 1 , the pharmaceutical composition being administered to at least one cell expressing G-protein-coupled receptor 40 (GPR40) and/or a polynucleotide encoding GPR40.

3. The method of claim 1 , the pharmaceutical composition promoting lipolysis in the subject.

4. The method of claim 1 , the pharmaceutical composition promoting hepatic uptake and esterification of free fatty acids.

5. The method of claim 1 , the pharmaceutical composition comprising at least one of (R)-all-trans-13,14-dihydroretinol, (S)-all-trans-13,14-dihydroretinol, (R)-all-trans-13,14-dihydroretinoic acid, or (S)-all-trans-13,14-dihydroretinoic acid, or an ester thereof.

6. The method of claim 1 , the pharmaceutical composition comprising at least 75% of (R)-all-trans-13,14-dihydroretinol, (R)-all-trans-13,14-dihydroretinoic acid, or an ester thereof.

7. The method of claim 1 , the pharmaceutical composition comprising at least 75% of (S)-all-trans-13,14-dihydroretinol, (S)-all-trans-13,14-dihydroretinoic acid, or an ester thereof.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 24, 2014
From: CASE WESTERN RESERVE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032329/0944 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2013
From: PALCZEWSKI, KRZYSZTOF; MOISE, RADU A.
To: CASE WESTERN RESERVE UNIVERSITY
Reel/Frame 029749/0741 →
Continuity (2)
Continuation 12445100 · Jan 20, 2010
Related Publication 20130072555A1 · Mar 21, 2013