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Mantle Cell Lymphoma

U.S. FDA approves Velcade for injection for aggressive form of non-Hodgkin lymphoma

Published in Cancer Weekly, January 16th, 2007

Millennium Pharmaceuticals, Inc. (MLNM) announced that the U.S. Food and Drug Administration (FDA) has granted full approval of Velcade for the treatment of patients with mantle cell lymphoma (MCL) who have received at least one prior therapy.

MCL is a relatively uncommon and aggressive form of non-Hodgkin lymphoma for which there was no standard of care in the relapsed or refractory setting. MCL has a U.S. prevalence of 10,000 patients. Velcade is currently the market leader in multiple myeloma (MM) for patients who have received one prior therapy. This approval marks the first indication for Velcade in lymphoma, the most common blood cancer.

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