IP Library Granted Patent US 10,953,011
Granted Patent B2
US 10,953,011 · App. 16/924,082 · Granted Mar 23, 2021

Methods of treating virally associated cancers with histone deacetylase inhibitors

Inventors: Robert McRae (Cardiff, CA); Gail L. Brown (Cardiff, CA); Xiaohu Deng (Cardiff, CA); David Slack (Cardiff, CA); Marshelle Smith Warren (Cardiff, CA); Richard Trauger (Cardiff, CA)
Assignee: VIRACTA THERAPEUTICS INC.
A61K31/506A61K31/522A61P35/00A61K9/0053A61K31/4709
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Quick Facts
Patent No.
US 10,953,011
App. No.
16/924,082
Granted
Mar 23, 2021
Kind
B2
Abstract

Described herein are certain dosing schedules and amounts that effectively prevent and manage side effects associated with histone deacetylase inhibitor (HDACi) treatment. Optionally, these schedules and dosing regimens include treatment with an antiviral agent.

Claims (25)

1. A method of treating an Epstein-Barr virus associated lymphoproliferative disorder in an individual, the method comprising administering to the individual: (a) nanatinostat at a total daily dose from 10 milligrams to 20 milligrams per day; and (b) an effective amount of an antiviral agent selected from the list consisting of aciclovir, ganciclovir, valaciclovir, valganciclovir, and famciclovir, wherein the individual is treated according to a treatment schedule having a duration of one week, and wherein the individual is administered nanatinostat for 4 days of the treatment schedule, thereby treating the Epstein-Barr virus associated lymphoproliferative disorder.

2. The method of claim 1 , wherein the nanatinostat is administered at a total daily dose of 10 milligrams.

3. The method of claim 1 , wherein the nanatinostat is administered at a total daily dose of 20 milligrams.

4. The method of claim 1 , wherein the nanatinostat is administered once per day.

5. The method of claim 1 , wherein the nanatinostat is administered twice per day.

6. The method of claim 1 , wherein the antiviral agent is valganciclovir.

7. The method of claim 6 , wherein the valganciclovir is administered at a total daily dose of 1,800 milligrams.

8. The method of claim 6 , wherein the valganciclovir is administered at a total daily dose of 900 milligrams.

9. The method of claim 6 , wherein the valganciclovir is administered at a total daily dose of 450 milligrams.

10. The method of claim 1 , wherein the antiviral agent is administered every day of the treatment schedule.

11. The method of claim 1 , wherein the antiviral agent is not administered on one or more days of the treatment schedule.

12. The method of claim 1 , wherein the antiviral agent is administered once a day.

13. The method of claim 1 , wherein the antiviral agent is administered twice a day.

14. The method of claim 1 , wherein the antiviral agent is administered orally.

15. The method of claim 1 , wherein the nanatinostat is administered orally.

16. The method of claim 1 , wherein the treatment schedule is repeated.

17. The method of claim 1 , wherein the Epstein-Barr virus associated lymphoproliferative disorder is an Epstein-Barr virus associated leukemia or a lymphoma.

18. The method of claim 17 , wherein the leukemia or lymphoma is a B cell or a T cell leukemia or lymphoma.

19. The method of claim 1 , wherein the individual is afflicted with thrombocytopenia.

20. The method of claim 1 , wherein the individual has a platelet count of less than 150,000 platelets per microliter.

21. A method of treating an Epstein-Barr virus associated lymphoproliferative disorder in an individual, the method comprising administering to the individual (a) nanatinostat at a total daily dose of about 20 mg; and (b) valganciclovir at a total daily dose of about 900 mg according to a weekly treatment schedule, wherein the individual is administered nanatinostat for 4 consecutive days of the treatment schedule, and valganciclovir is administered every day of the treatment schedule.

22. The method of claim 21 , wherein nanatinostat and valganciclovir are administered orally.

23. The method of claim 21 , wherein nanatinostat and valganciclovir are each administered once a day.

24. The method of claim 21 , wherein nanatinostat and valganciclovir are each administered twice a day.

25. The method of claim 21 , wherein the treatment schedule is repeated.

Assignments (4)
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jan 23, 2025
From: VIRACTA SUBSIDIARY, INC.
To: OXFORD FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 070000/0001 →
CHANGE OF NAME Recorded May 25, 2022
From: VIRACTA THERAPEUTICS, INC.
To: VIRACTA SUBSIDIARY, INC.
Reel/Frame 060200/0772 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2021
From: MCRAE, ROBERT; BROWN, GAIL L.; DENG, XIAOHU; SLACK, DAVID; WARREN, MARSHELLE SMITH; TRAUGER, RICHARD
To: VIRACTA THERAPEUTICS, INC.
Reel/Frame 055528/0125 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2020
From: MCRAE, ROBERT; BROWN, GAIL L.; DENG, XIAOHU; SLACK, DAVID; WARREN, MARSHELLE SMITH; TRAUGER, RICHARD
To: VIRACTA THERAPEUTICS, INC.
Reel/Frame 053640/0628 →
Continuity (3)
Continuation PCTUS2020034951 · May 28, 2020
Provisional Application 62855454 · May 31, 2019
Related Publication 20200375990A1 · Dec 3, 2020