FDA granted accelerated approval to pomalidomide (POMALYST capsules, Celgene Corporation) for the treatment of patients with multiple myeloma who have received at least two prior therapies, including lenalidomide and bortezomib, and have demonstrated disease progression on or within 60 days of completion of the last therapy. February 8, 2013 More Information: http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm339286.htm
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