US FDA approves sNDAs for Imbruvica and Azilect

9 June 2014

USA-based Pharmacyclics (Nasdaq: PCYC) says that the US Food and Drug Administration has accepted for filing its supplemental New Drug Application (sNDA) to support the review of Imbruvica (ibrutinib) in the treatment of patients with chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL) who have received at least one prior therapy for a full approval.

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