IP Library Granted Patent US 9,308,186
Granted Patent B2
US 9,308,186 · App. 13/323,510 · Granted Apr 12, 2016

Treatment of cancer with specific RXR agonists

Inventor: Roshantha A. Chandraratna (Laguna Hills, CA)
Assignee: IO Therapeutics, Inc.
A61K31/192A61K45/06
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Quick Facts
Patent No.
US 9,308,186
App. No.
13/323,510
Granted
Apr 12, 2016
Kind
B2
Abstract

A method of treating cancer is disclosed comprising administering to a patient in need of such treatment a RXR agonist at a level below the RAR activating threshold and at or above the RXR effective dose.

Claims (13)

1. A method of treating cancer, the method comprising administering to a patient in need of such treatment a retinoid X receptor (RXR) agonist at a dose which does not activate retinoic acid receptors (RAR) and wherein the dose of the RXR agonist is from about 1 to about 20 mg/m 2 /day, and the cancer is lung cancer;

wherein the RXR agonist has a chemical structure

or a pharmaceutically acceptable salt thereof.

2. The method according to claim 1 , wherein the dose is determined by dosing the patient with increasing concentrations of a RXR agonist until an RXR effective dose is reached which does not activate RAR.

3. The method according to claim 1 , wherein the RXR effective dose is determined by measuring the reduction of a patient's TSH levels.

4. The method according to claim 1 , wherein RAR activation is determined by measuring at least one RAR biomarker expressed by the patient.

5. The method according to claim 4 , wherein the RAR biomarker is selected from the group consisting of CYP26 level, CRBPI level and combinations thereof.

6. The method according to claim 1 , further comprising measuring the patient's C max of the RXR agonist, and adjusting the dose to maintain the patient's C max at an optimal level.

7. The method according to claim 1 , further comprising treating the patient with at least one other agent selected from the group consisting of anti-cancer agents, triglyceride lowering agents and TSH modulating agents.

8. The method according to claim 7 , wherein the anti-cancer agent is selected from the group consisting of a platinum-based compound, a cytotoxic drug, and mixtures thereof.

9. The method according to claim 1 , wherein the dose of the RXR agonist is from about 1 to about 10 mg/m 2 /day.

10. The method according to claim 1 , wherein the dose of the RXR agonist is from about 10 to about 20 mg/m 2 /day.

11. The method according to claim 1 , wherein the RXR agonist is 3,7-di methyl-6(S),7(S)-methano,7-[1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphth-7-yl]2(E),4(E) heptadienoic acid.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2012
From: CHANDRARATNA, ROSHANTHA A.
To: IO THERAPEUTICS, INC.
Reel/Frame 027607/0816 →
Continuity (4)
Division 12079938 · Mar 28, 2008
Continuation In Part PCTUS2006038252 · Oct 2, 2006
Provisional Application 60722264 · Sep 30, 2005
Related Publication 20120094956A1 · Apr 19, 2012