IP Library Granted Patent US 10,201,512
Granted Patent B2
US 10,201,512 · App. 15/852,580 · Granted Feb 12, 2019

Autoimmune disorder treatment using RXR agonists

Inventors: Roshantha A. Chandraratna (San Juan Capistrano, CA); Ethan Dmitrovsky (Hanover, NH); Elizabeth Nowak (West Lebanon, NH); Randolph Noelle (Plainfield, NH)
Assignee: IO Therapeutics, Inc.
A61K31/192A61K9/0073A61K31/201A61K31/216A61K31/343A61K31/353A61K31/47A61K31/4704
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Quick Facts
Patent No.
US 10,201,512
App. No.
15/852,580
Granted
Feb 12, 2019
Kind
B2
Abstract

The present specification provides RXR agonist compounds, compositions comprising such RXR agonists, and methods using such compounds and compositions to treat an autoimmune disorder, inflammation associated with an autoimmune disorder and/or a transplant rejection as well as use of such RXR agonists to manufacture a medicament and use of such compounds and compositions to treat an autoimmune disorder, inflammation associated with an autoimmune disorder and/or a transplant rejection.

Claims (15)

1. A method of treating multiple sclerosis, the method comprising elevating Treg cell numbers and suppressing Th17 cell numbers in an individual having multiple sclerosis by administering a therapeutically effective amount of a retinoid X receptor (RXR) agonist having the structure of formula XII:

or a pharmaceutically acceptable salt thereof;

wherein R is H or lower alkyl of 1 to 6 carbons,

wherein the therapeutically effective amount is about 0.001 mg/kg/day to about 100 mg/kg/day;

whereby the balance between Treg and Th17 cell development is modulated to restrain autoimmunity.

2. The method according to claim 1 , wherein the RXR agonist is 3,7-dimethyl-6(S),7(S)-methano,7-[1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphth-7-yl]2(E),4(E) heptadienoic acid, and has the structure of formula XXIX:

or a pharmaceutically acceptable salt thereof.

3. The method according to claim 1 , wherein the therapeutically effective amount is about 0.001 mg/kg/day to about 0.2 mg/kg/day.

4. The method according to claim 1 , wherein the therapeutically effective amount is about 0.1 mg/kg/day to about 3.0 mg/kg/day.

5. The method according to claim 1 , wherein R is H.

6. The method according to claim 2 , wherein the RXR agonist is a salt of the compound of formula XXIX.

7. The method according to claim 1 , wherein the RXR agonist is administered by inhalation.

8. The method of claim according to claim 1 , wherein the therapeutically effective amount is about 0.01 mg/kg/day to about 0.1 mg/kg/day.

9. The method according to claim 1 , wherein elevating Treg cell numbers comprises promoting differentiation of Treg cells.

10. The method according to claim 1 , wherein suppressing Th17 cell numbers comprises inhibiting Th17 cell differentiation.

Assignments (3)
CONFIRMATORY LICENSE Recorded Dec 20, 2018
From: DARMOUTH COLLEGE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 047968/0056 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2017
From: CHANDRARATNA, ROSHANTHA A.
To: IO THERAPEUTICS, INC.
Reel/Frame 044471/0511 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2017
From: DMITROVSKY, ETHAN; NOWAK, ELIZABETH; NOELLE, RANDOLPH J.
To: TRUSTEES OF DARTMOUTH COLLEGE
Reel/Frame 044471/0582 →
Continuity (4)
Continuation 15341969 · Nov 2, 2016
Continuation 13714051 · Dec 13, 2012
Provisional Application 61570182 · Dec 13, 2011
Related Publication 20180116985A1 · May 3, 2018