IP Library Granted Patent US 10,300,073
Granted Patent B2
US 10,300,073 · App. 15/517,476 · Granted May 28, 2019

Use of CDK9 and BRD4 inhibitors to inhibit inflammation

Inventors: Dominik Haudenschild (Davis, CA); Jasper Yik (Elk Grove, CA)
Assignee: The Regents of the University of California
A61K31/5513A61K31/352A61K31/445A61K31/551A61K45/06A61K31/00
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Quick Facts
Patent No.
US 10,300,073
App. No.
15/517,476
Granted
May 28, 2019
Kind
B2
Abstract

Provided are methods for the combined use of cyclin-dependent kinase 9 (CDK9) inhibitors and bromodomain containing 4 (BRD4) inhibitors to reduce, inhibit and/or prevent cartilage degradation and systemic traumatic inflammation. A combination of CDK9 inhibitors and BRD4 inhibitors can be used to reduce, inhibit and/or prevent cartilage degradation and loss of cartilage viability during allograft storage. A combination of CDK9 inhibitors and BRD4 inhibitors can be used as a post-injury intervention treatment to reduce, inhibit and/or prevent the acute cellular responses that lead to future cartilage degradation and osteoarthritis.

Claims (27)

1. A method of reducing, inhibiting, mitigating and/or ameliorating cartilage degradation and/or chondrocyte death in a subject in need thereof, comprising co-administering to the subject an effective amount of an inhibitor of cyclin-dependent kinase 9 (CDK9) and an inhibitor of bromodomain containing protein 4 (BRD4), thereby reducing, inhibiting, mitigating and/or ameliorating cartilage degradation and/or chondrocyte death in the subject, wherein the CDK9 inhibitor and the BRD4 inhibitor are initially co-administered within about 10 day after experiencing traumatic injury.

2. The method of claim 1 , wherein the subject has experienced a traumatic injury to cartilage tissue.

3. The method of claim 2 , wherein the subject has undergone joint surgery.

4. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are initially co-administered during the acute response phase and reduce and/or inhibit transcriptional activation of one or more primary response genes after experiencing traumatic injury.

5. The method of claim 4 , wherein the one or more primary response genes are selected from the group consisting of IL-1β, inducible nitric oxide synthase (iNOS), IL-6, TNF-α, MMP-1, MMP-3, MMP-9, MMP-13 and ADAMTS4 (aggrecanase).

6. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are initially co-administered within about 72 hours after experiencing traumatic injury.

7. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are administered over a course of 10 days.

8. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are administered multiple times.

9. The method of claim 1 , wherein the subject has undergone surgery to repair damaged cartilage tissue.

10. The method of claim 1 , wherein the subject has received an osteochondral explant.

11. The method of claim 10 , wherein the osteochondral explant is a cartilage allograft.

12. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are co-administered concurrently with or prior to surgery.

13. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are co-administered within 24 hours after surgery.

14. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are co-administered systemically.

15. The method of claim 14 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are co-administered intravenously.

16. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are co-administered directly to the site of injured cartilage tissue.

17. The method of claim 16 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are delivered from a matrix.

18. The method of claim 1 , wherein the inhibitor of CDK9 is a small organic compound.

19. The method of claim 18 , wherein the inhibitor of CDK9 is flavopiridol.

20. The method of claim 1 , wherein the inhibitor of BRD4 is a small organic compound.

21. The method of claim 20 , wherein the inhibitor of BRD4 is selected from the group consisting of JQ1 (CAS Number 1268524-70-4) and GSK525762A (CAS Number 1260907-17-2).

22. The method of claim 1 , wherein one or both of the inhibitor of CDK9 and the inhibitor of BRD4 are administered at a subtherapeutic or non-efficacious dose for the individual inhibitors.

23. A method of reducing, inhibiting, mitigating and/or ameliorating the onset and/or progression of post-traumatic osteoarthritis in a subject in need thereof, comprising co-administering to the subject an effective amount of an inhibitor of cyclin-dependent kinase 9 (CDK9) and an inhibitor of bromodomain containing protein 4 (BRD4), thereby reducing, inhibiting, mitigating and/or ameliorating post-traumatic osteoarthritis in the subject, wherein the CDK9 inhibitor and the BRD4 inhibitor are initially co-administered within about 10 days after experiencing traumatic injury.

24. A method of reducing, inhibiting, mitigating and/or ameliorating severe polytrauma or systemic inflammatory response syndrome (SIRS) in a subject in need thereof, comprising administering to the subject an effective amount of an inhibitor of cyclin-dependent kinase 9 (CDK9) and an inhibitor of bromodomain containing protein 4 (BRD4), thereby reducing, inhibiting, mitigating and/or ameliorating severe polytrauma or systemic inflammatory response syndrome (SIRS) in the subject, wherein the CDK9 inhibitor and the BRD4 inhibitor are initially co-administered within about 10 days after experiencing traumatic injury.

25. A method of reducing, inhibiting, mitigating and/or ameliorating severe polytrauma or systemic inflammatory response syndrome (SIRS) in a subject in need thereof, comprising co-administering to the subject an effective amount of an inhibitor of cyclin-dependent kinase 9 (CDK9) and an inhibitor of bromodomain containing protein 4 (BRD4), thereby reducing, inhibiting, mitigating and/or ameliorating severe polytrauma or systemic inflammatory response syndrome (SIRS) in the subject, wherein the CDK9 inhibitor and the BRD4 inhibitor are initially co-administered within about 10 days after experiencing traumatic injury.

26. A method of reducing, or inhibiting degradation of an osteochondral explant and/or reducing, preventing or inhibiting chondrocyte death during storage, comprising storing the osteochondral explant and/or chondrocytes in a solution comprising an inhibitor of cyclin-dependent kinase 9 (CDK9) and an inhibitor of bromodomain containing protein 4 (BRD4).

27. A composition comprising an osteochondral explant in a solution comprising an inhibitor of cyclin-dependent kinase 9 (CDK9) and an inhibitor of bromodomain containing protein 4 (BRD4).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2017
From: HAUDENSCHILD, DOMINIK; YIK, JASPER
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 042017/0246 →
Continuity (2)
Provisional Application 62063839 · Oct 14, 2014
Related Publication 20170304315A1 · Oct 26, 2017
Cited By (1)
US 12,685,777