IP Library Granted Patent US 10,945,976
Granted Patent B2
US 10,945,976 · App. 16/228,217 · Granted Mar 16, 2021

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)
Assignees: Io Therapeutics, Inc.; Trustees of Dartmouth College
A61K31/192A61K9/0073A61K31/201A61K31/216A61K31/343A61K31/353A61K31/47A61K31/4704Y02A50/30
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Quick Facts
Patent No.
US 10,945,976
App. No.
16/228,217
Granted
Mar 16, 2021
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 (30)

1. A method of treating schizophrenia, the method comprising elevating Treg cell numbers and suppressing Th17 cell numbers in an individual having schizophrenia 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. A method of treating an autoimmune aspect of schizophrenia, the method comprising concurrently promoting differentiation of Treg cells and inhibiting differentiation of Th17 cells using a single agent by administering to an individual having schizophrenia 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;

wherein the autoimmune aspect comprises inflammation or Th17 to Treg cell ratio;

whereby the autoimmune aspect of schizophrenia is reduced.

8. The method according to claim 7 , 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.

9. The method according to claim 7 , wherein the therapeutically effective amount is about 0.001 mg/kg/day to about 0.2 mg/kg/day.

10. The method according to claim 7 , wherein the therapeutically effective amount is about 0.1 mg/kg/day to about 3.0 mg/kg/day.

11. The method according to claim 7 , wherein R is H.

12. The method according to claim 8 , wherein the RXR agonist is a salt of the compound of formula XXIX.

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

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

15. 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.

16. The method of claim according to claim 7 , wherein the therapeutically effective amount is about 0.01 mg/kg/day to about 0.1 mg/kg/day.

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

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

19. The method according to claim 7 , wherein the ratio of Th17 cells to Treg cells is decreased.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2018
From: DMITROVSKY, ETHAN; NOWAK, ELIZABETH; NOELLE, RANDOLPH J.
To: TRUSTEES OF DARTMOUTH COLLEGE
Reel/Frame 047836/0108 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2018
From: CHANDRARATNA, ROSHANTHA A.
To: IO THERAPEUTICS, INC.
Reel/Frame 047836/0185 →
Continuity (5)
Continuation 15852580 · Dec 22, 2017
Continuation 15341969 · Nov 2, 2016
Continuation 13714051 · Dec 13, 2012
Provisional Application 61570182 · Dec 13, 2011
Related Publication 20190125705A1 · May 2, 2019