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IMBRUVICA Capsules Gain Approval in CLL

By Kristin Brooks | February 14, 2014

Catalent to provide commercial supply from Kansas City site

IMBRUVICA (ibrutinib) has been approved by the FDA as a single, oral agent for the treatment of patients with chronic lymphocytic leukemia (CLL) who have received at least one prior therapy. The drug was originally approved on November 13, 2013 for the treatment of patients with mantle cell lymphoma (MCL) who have received at least one prior therapy.
 
Catalent Pharma Solutions has been contracted by Pharmacyclics to provide drug product capsules of IMBRUVICA for commercial supply from its site in Kansas City, MO.

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