FDA Approves New Indication for Tasigna

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Title: FDA Approves New Indication for Tasigna

FDA Approves New Indication for Tasigna
Thu, 17 Jun 2010 16:04:00 -0500

The U.S. Food and Drug Administration today approved a new indication for Tasigna (nilotinib) for the treatment of a rare blood cancer when it is first diagnosed. The cancer, called Philadelphia chromosome positive chronic phase chronic myeloid leukemia (Ph+ CP-CML), is a slowly progressing blood and bone marrow disease linked to a genetic abnormality.


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