US FDA approves additional medical indication for Bristol-Myers Squibb's Sprycel; clears Sunovion's Latuda; further delays Vivus' Qnexa
The US Food and Drug Administration yesterday approved a new indication for drug major Bristol-Myers Squibb’s (NYSE: BMY) Sprycel (dasatinib) 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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