Phase III Trial of ICLUSIG® (Ponatinib) Met Primary Endpoint in Newly-Diagnosed Ph+ ALL, a Setting with No Targeted Treatments Approved in the US

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Takeda announced that the Phase III PhALLCON trial met its primary endpoint, demonstrating that adult patients with newly-diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) treated with ICLUSIG® (ponatinib) plus chemotherapy achieved higher rates of minimal residual disease-negative complete remission compared to imatinib.
[Takeda]
Press Release