IP Library Granted Patent US 11,612,609
Granted Patent B2
US 11,612,609 · App. 16/983,492 · Granted Mar 28, 2023

Uses of oxygenated cholesterol sulfates (OCS)

Inventors: Shunlin Ren (Richmond, VA); Felix Theeuwes (Los Altos Hills, CA); James E. Brown (Los Gatos, CA); WeiQi Lin (Emerald Hills, CA)
Assignees: Durect Corporation; Virginia Commonwealth University
A61K31/575A01N1/0226A61K31/568A61K35/12A61P13/12
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Quick Facts
Patent No.
US 11,612,609
App. No.
16/983,492
Granted
Mar 28, 2023
Kind
B2
Abstract

Methods of preventing and/or treating ischemia, organ dysfunction and/or organ failure, including multiple organ dysfunction syndrome (MODS), and necrosis and apoptosis associated with organ dysfunction/failure, are provided. For instance, the methods involve contacting organ(s) with an oxygenated cholesterol sulfate (OCS), e.g. 5-cholesten-3,25-diol, 3-sulfate (25H-C3S). The organ(s) may be in vivo (e.g. in a patient that is treated with the OCS) or ex vivo (e.g. an organ that has been harvested from a donor and is to be transplanted).

Claims (22)

1. A method of treating acute liver dysfunction or acute liver failure in a human subject in need thereof, comprising

administering to the human subject an amount of a sodium salt of 5-cholesten-3,25-diol, 3-sulfate (25HC3S) that is sufficient to treat the acute liver dysfunction or acute liver failure, wherein the acute liver dysfunction or acute liver failure comprises alcoholic hepatitis.

2. The method of claim 1 , wherein the alcoholic hepatitis is characterized by reduced liver function that occurs within 13 weeks of onset.

3. The method of claim 1 , wherein the alcoholic hepatitis is characterized by reduced liver function that occurs within 10 weeks of onset.

4. The method of claim 1 , wherein the alcoholic hepatitis is characterized by loss of liver function that occurs within 13 weeks of onset.

5. The method of claim 1 , wherein the alcoholic hepatitis is characterized by loss of liver function that occurs within 10 weeks of onset.

6. The method of claim 1 , wherein the administering is performed by at least one of orally, subcutaneously, and intramuscularly.

7. The method of claim 1 , wherein the administering is performed intravenously.

8. The method of claim 1 , wherein the administering comprises injection.

9. The method of claim 1 , wherein the sodium salt of 25HC3S is administered in a formulation further comprising a pharmaceutically acceptable carrier.

10. The method of claim 1 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 100 mg/kg.

11. The method of claim 1 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

12. The method of claim 1 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.1 mg/kg to about 10 mg/kg.

13. The method of claim 1 , wherein the administering is performed from once to 3 times per day.

14. The method of claim 2 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

15. The method of claim 3 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

16. The method of claim 4 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

17. The method of claim 5 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

18. The method of claim 7 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

19. The method of claim 8 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

20. The method of claim 9 , wherein the sodium salt of 25HC3S is administered at a dose ranging from about 0.001 mg/kg to about 10 mg/kg.

21. The method of claim 1 , wherein the human subject has jaundice prior to treatment.

Assignments (6)
SECURITY INTEREST Recorded Mar 30, 2026
From: BAUSCH HEALTH IRELAND LIMITED; MEDICIS PHARMACEUTICAL CORPORATION; SALIX PHARMACEUTICALS, INC.; SOLTA MEDICAL IRELAND LIMITED
To: THE BANK OF NEW YORK MELLON
Reel/Frame 074223/0753 →
SECURITY INTEREST Recorded Mar 30, 2026
From: MEDICIS PHARMACEUTICAL CORPORATION
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 074227/0509 →
MERGER Recorded Feb 25, 2026
From: DURECT CORPORATION
To: MEDICIS PHARMACEUTICAL CORPORATION
Reel/Frame 073889/0196 →
MERGER Recorded Feb 19, 2026
From: DURECT CORPORATION
To: MEDICIS PHARMACEUTICAL CORPORATION
Reel/Frame 073837/0231 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2023
From: VIRGINIA COMMONWEALTH UNIVERSITY
To: THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS; VIRGINIA COMMONWEALTH UNIVERSITY
Reel/Frame 062318/0868 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2021
From: REN, SHUNLIN; THEEUWES, FELIX; BROWN, JAMES E.; LIN, WEIQI
To: VIRGINIA COMMONWEALTH UNIVERSITY; DURECT CORPORATION
Reel/Frame 055626/0551 →
Cited By (3)
US 12,226,423 US 12,642,805 US 12,692,288