IP Library Granted Patent US 10,022,342
Granted Patent B2
US 10,022,342 · App. 15/254,900 · Granted Jul 17, 2018

Methods and compositions for treating multiple myeloma

Inventors: Flavia Pichiorri (Columbus, OH); Craig Hofmeister (Upper Arlington, OH)
Assignee: OHIO STATE INNOVATION FOUNDATION
A61K31/167A61K31/454
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Quick Facts
Patent No.
US 10,022,342
App. No.
15/254,900
Granted
Jul 17, 2018
Kind
B2
Abstract

Methods and compositions for sensitizing multiple myeloma cells to treatment with IMiDs are provided. Aspects include methods of administering AR-42 and an IMiD (e.g., lenalidomide, pomalidomide) to multiple myeloma patients.

Claims (12)

1. A method of sensitizing multiple myeloma cells to treatment with lenalidomide comprising administering AR-42 and lenalidomide to a patient in need treatment in an amount sufficient to achieve a blood or tissue concentration of at least about 0.5 to about 1 μM of AR-42 and at least about 391 to about 568 ng/ml of lenalidomide.

2. The method of claim 1 , wherein the amount of AR-42 administered to the patient is about 40 to 70 mg in a single dose or divided dose, three times per week for three weeks out of a 28 day cycle.

3. The method of claim 2 , wherein the amount of AR-42 administered to the patient is about 0.6 to about 1.1 mg/kg of the patient.

4. The method claim 2 , wherein the amount of lenalidomide administered to the patient is about 25 mg per day for days 1-21 of a 28 day cycle.

5. A method of treating a mammal with multiple myeloma comprising administering AR-42 and an immunomodulatory agent selected from the group consisting of lenalidomide and pomolidomide to the mammal.

6. The method of claim 5 , wherein the amount of AR-42 administered to the mammal is about 40 to 70 mg in a single dose or divided dose, three times per week for three weeks out of a 28 day cycle.

7. The method of claim 6 , wherein the amount of AR-42 administered to the patient is about 0.6 to about 1.1 mg/kg of the patient.

8. The method of claim 5 , wherein AR-42 and the immunomodulatory agent are co-administered to the mammal.

9. The method of claim 5 , wherein AR-42 is administered before administering the immunomodulatory agent.

10. The method of claim 5 , wherein the immunomodulatory agent is administered before administering AR-42.

11. The method of claim 5 , where the amount of lenalidomide administered to the mammal is about 25 mg per day for days 1-21 of a 28 day cycle.

12. The method of claim 5 , where the amount of pomalidomide administered to the mammal is about 4 mg per day for days 1-21 of a 28 day cycle.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 16, 2018
From: OHIO STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046548/0396 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2017
From: PICHIORRI, FLAVIA; HOFMEISTER, CRAIG
To: OHIO STATE INNOVATION FOUNDATION
Reel/Frame 043002/0328 →
Continuity (2)
Provisional Application 62213493 · Sep 2, 2015
Related Publication 20170056346A1 · Mar 2, 2017