Details for Patent: 9,662,321

Title:	Methods for treating newly diagnosed multiple myeloma with 3-(4-amino-1-OXO-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione in combination with second active agents
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:	Celgene Corporation (Summit, NJ)
Filing Date:	May 20, 2016
Application Number:	15/161,048
Claims:	1. A method of treating multiple myeloma, which comprises administering in a 28 day cycle to a patient having multiple myeloma: (a) about 1 to about 50 mg per day of a compound having the formula: ##STR00009## or a pharmaceutically acceptable salt, solvate or stereoisomer thereof for 21 consecutive days followed by seven consecutive days of rest from administration of the compound, (b) a therapeutically effective amount of dexamethasone during the 28 day cycle, and (c) a therapeutically effective amount of a proteasome inhibitor during the 28 day cycle. 2. The method of claim 1, wherein the multiple myeloma is newly diagnosed. 3. The method of claim 1, wherein the multiple myeloma is relapsed, refractory, or relapsed and refractory. 4. The method of claim 1, wherein the patient is eligible for stem cell transplantation. 5. The method of claim 1, wherein the patient is ineligible for stem cell transplantation. 6. The method of claim 1, wherein the patient has received prior therapy for multiple myeloma. 7. The method of claim 6, wherein the patient has received stem cell transplantation. 8. The method of claim 1, wherein the compound is ##STR00010## and is not a pharmaceutically acceptable salt, solvate or stereoisomer thereof. 9. The method of claim 1, wherein the compound is a pharmaceutically acceptable salt. 10. The method of claim 1, wherein the compound is a pharmaceutically acceptable solvate. 11. The method of claim 1, wherein the compound is a pharmaceutically acceptable stereoisomer. 12. The method of claim 1, wherein the compound is administered in an amount of about 25 mg per day. 13. The method of claim 1, wherein the compound is administered in an amount of about 20 mg per day. 14. The method of claim 1, wherein the compound is administered in an amount of about 15 mg per day. 15. The method of claim 1, wherein the compound is administered in an amount of about 10 mg per day. 16. The method of claim 1, wherein the compound is administered in an amount of about 5 mg per day. 17. The method of claim 1, wherein the compound is administered in an amount of about 2.5 mg per day. 18. The method of claim 1, wherein the compound is administered orally. 19. The method of claim 18, wherein the compound is administered in the form of a capsule or tablet. 20. The method of claim 19, wherein the compound is administered in a capsule in an amount from about 1 mg to about 25 mg. 21. The method of claim 20, wherein the compound is administered in a capsule in an amount of about 2.5 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg or about 25 mg. 22. The method of claim 21, wherein the capsule comprises the compound, lactose anhydrous, microcrystalline cellulose, croscarmellose sodium and magnesium stearate. 23. The method of claim 1, which further comprises administering a therapeutically effective amount of an additional active agent. 24. The method of claim 23, wherein the additional active agent is melphalan, doxorubicin, vincristine, prednisone, cyclophosphamide, biaxin, or a combination thereof. 25. The method of claim 1, wherein the solvate is hydrate.