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Details for Patent: 9,155,730

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Details for Patent: 9,155,730

Title:Methods for treating non-hodgkin's lymphoma with 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione in combination with a second active agent
Abstract: Methods of treating, preventing and/or managing cancer as well as and diseases and disorders associated with, or characterized by, undesired angiogenesis are disclosed. Specific methods encompass the administration of an immunomodulatory compound alone or in combination with a second active ingredient. The invention further relates to methods of reducing or avoiding adverse side effects associated with chemotherapy, radiation therapy, hormonal therapy, biological therapy or immunotherapy which comprise the administration of an immunomodulatory compound. Pharmaceutical compositions, single unit dosage forms, and kits suitable for use in methods of the invention are also disclosed.
Inventor(s): Zeldis; Jerome B. (Princeton, NJ)
Assignee: Calgene Corporation (Summit, NJ)
Filing Date:Mar 26, 2014
Application Number:14/225,970
Claims:1. A method of treating non-Hodgkin's lymphoma, which comprises (a) administering to a patient having non-Hodgkin's lymphoma from about 1 to about 50 mg per day of a compound having the formula: ##STR00009## or a pharmaceutically acceptable salt, solvate or stereoisomer thereof, and a therapeutically effective amount of a second active agent; followed by (b) administering to the patient about 1 to about 50 mg per day of the compound, wherein the non-Hodgkin's lymphoma is follicular lymphoma.

2. The method of claim 1, wherein the non-Hodgkin's lymphoma is relapsed, refractory, or relapsed and refractory.

3. The method of claim 1, wherein the compound is ##STR00010##

4. The method of claim 1, wherein the compound is a pharmaceutically acceptable salt.

5. The method of claim 1, wherein the compound is a pharmaceutically acceptable solvate.

6. The method of claim 1, wherein the compound is a pharmaceutically acceptable stereoisomer.

7. The method of claim 1, wherein the second active agent is rituximab, vinblastine, fludarabine, cyclophosphamide, vincristine, doxorubicin, prednisone, a proteasome inhibitor, or a combination thereof.

8. The method of claim 1, wherein the second active agent is rituximab.

9. The method of claim 1, wherein the compound is administered cyclically.

10. The method of claim 1, wherein the compound is administered for about one to about 24 cycles.

11. The method of claim 1, wherein the compound is administered for 21 consecutive days followed by 7 consecutive days of rest in a 28 day cycle.

12. The method of claim 1, wherein the compound is administered until disease progression or unacceptable toxicity.

13. The method of claim 1, wherein the compound is administered in an amount from about 1 to about 25 mg per day.

14. The method of claim 13, wherein the compound is administered in an amount of about 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg or 25 mg per day.

15. The method of claim 1, wherein the compound is administered in an amount of about 20 mg per day.

16. The method of claim 1, wherein the compound is administered in an amount of about 10 mg per day.

17. The method of claim 1, wherein the compound is administered in an amount of about 20 mg per day in (a).

18. The method of claim 1, wherein the compound is administered in an amount of about 10 mg per day in (b).

19. The method of claim 1, wherein the compound is administered orally.

20. The method of claim 19, wherein the compound is administered in the form of a capsule or tablet.

21. The method of claim 20, wherein the compound is administered in a capsule in an amount from about 1 mg to about 50 mg.

22. The method of claim 21, wherein the compound is administered in a capsule in an amount of about 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg or 25 mg.

23. The method of claim 20, wherein the capsule comprises the compound, lactose anhydrous, microcrystalline cellulose, croscarmellose sodium and magnesium stearate.

24. The method of claim 8, wherein the rituximab is administered cyclically.

25. A method of treating non-Hodgkin's lymphoma, which comprises (a) administering to a patient having non-Hodgkin's lymphoma from about 1 to about 50 mg per day of a compound having the formula: ##STR00011## or a pharmaceutically acceptable salt, solvate or stereoisomer thereof for 21 consecutive days followed by 7 consecutive days of rest in a 28-day cycle, and a therapeutically effective amount of rituximab; followed by (b) administering to the patient from about 5 to about 25 mg per day of the compound for 21 consecutive days followed by 7 consecutive days of rest in a 28-day cycle, wherein the non-Hodgkin's lymphoma is follicular lymphoma.

26. The method of claim 25, wherein the non-Hodgkin's lymphoma is relapsed, refractory, or relapsed and refractory.

27. The method of claim 25, wherein the compound is administered orally in an amount of about 20 mg per day in (a).

28. The method of claim 25, wherein the compound is administered orally in an amount of about 10 mg per day in (b).
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