IP Library Granted Patent US 9,480,664
Granted Patent B2
US 9,480,664 · App. 14/809,859 · Granted Nov 1, 2016

Compositions and methods for treating cancer

Inventor: Mong-Heng Wang (Martinez, GA)
Assignee: Augusta University Research Institute, Inc.
A61K31/155A61K31/365A61K31/5575A61K45/06
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Quick Facts
Patent No.
US 9,480,664
App. No.
14/809,859
Granted
Nov 1, 2016
Kind
B2
Abstract

Compositions containing one or more COX inhibitors in combination with one or more antagonists of 20-HETE (20-hydroxyeicosatetraeonic acid), and optionally a pharmaceutically acceptable excipient are provided. Preferred compositions include rofecoxib in combination with HET0016. The compositions have reduced side effects due to COX inhibitors. Methods for treating or inhibiting cancer using the disclosed compositions are also provided.

Claims (14)

1. A pharmaceutical composition comprising an effective amount of a COX-2 inhibitor to inhibit cancer cell growth in a subject in need thereof in combination with a 20-Hydroxyeicosatetraenoic acid (20-HETE) antagonist in an effective amount to reduce or inhibit side effects of the COX-2 inhibitor in the subject, wherein the COX-2 inhibitor is selected from the group consisting celecoxib, rofecoxib, etoricoxib, valdecoxib, 4-[5-(4-methylphenyl)-3-(methylselenocyano)-1H-pyrazol-1-yl]benzene-sulfonamide, 4-[5-(4-(methylselenomethylene)phenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzene-sulfonamide and 2,5-dimethyl-celecoxib and wherein the 20-HETE antagonist is selected from the group consisting of 20-hydroxyeicosa-6(Z),15(Z)-dienoic acid (WIT002), N-Hydroxy-N′-(4-butyl-2-methylphenyl)formamidine (HET0016), 17-octadecynoic acid (17-ODYA), N-methylsulfonyl-12,12-dibromododec-11-enamide (DDMS), dibromododec-11-enoic acid (DDBB), N-(3-Chloro-4-morpholin-4-yl)Phenyl-N′-hydroxyimido formamide (TS011), 20-hydroxyeicosa-6(Z),15 (Z)-dienoic acid (6-,15-,20-HEDE) and (N-[20-hydroxyeicosa-5 (Z), and 14 (Z)-dienoic acid (5, 14, 20-HEDGE).

2. The pharmaceutical composition of claim 1 , further comprising an excipient.

3. The pharmaceutical composition of claim 1 or 2 , wherein the COX-2 inhibitor is rofecoxib and the 20-HETE blocker is HET0016.

4. The pharmaceutical composition of claim 1 , wherein the side effects are selected from the group consisting of myocardial infarction, arterial and venous thrombic events, ischemic stroke, and arrhythmia.

5. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated for enteral administration.

6. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated for parenteral administration.

7. A method for inhibiting cancer cell growth in a subject, comprising:

administering to the subject the pharmaceutical composition of claim 1 .

8. A method for reducing the reoccurrence of cancer in a subject, comprising:

administering the pharmaceutical composition of claim 1 to the subject.

9. The method of claim 8 , wherein the cancer is colorectal cancer.

10. The method of claim 9 , wherein a colorectal adenoma or poly is removed from the subject prior to administration of the pharmaceutical composition.

11. A method for reducing the reoccurrence of colorectal adenoma in a subject in need thereof, comprising:

administering the pharmaceutical composition of claim 1 to the subject.

Assignments (3)
CHANGE OF NAME Recorded May 18, 2016
From: GEORGIA REGENTS RESEARCH INSTITUTE, INC.
To: AUGUSTA UNIVERSITY RESEARCH INSTITUTE, INC.
Reel/Frame 038743/0980 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2015
From: WANG, MONG-HENG
To: GEORGIA REGENTS UNIVERSITY
Reel/Frame 036237/0089 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2015
From: GEORGIA REGENTS UNIVERSITY
To: GEORGIA REGENTS RESEARCH INSTITUTE, INC.
Reel/Frame 036237/0114 →
Continuity (2)
Provisional Application 62028835 · Jul 25, 2014
Related Publication 20160022614A1 · Jan 28, 2016