ICLUSIG® (Ponatinib)

ICLUSIG® (Ponatinib): The FDA on December 17, 2012 granted accelerated approval to ICLUSIG® for the treatment of adult patients with chronic phase, accelerated phase, or blast phase chronic myeloid leukemia (CML) that is resistant or intolerant to prior tyrosine kinase inhibitor therapy or Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ALL) that is resistant or intolerant to prior tyrosine kinase inhibitor therapy. ICLUSIG® is available as oral tablets and is a product of ARIAD Pharmaceuticals, Inc.