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Full 12 weeks of medication, shipping, consultation, and injection kit

What Was Approved

03/19/24 Iclusig (ponatinib) Expanded indication March 19, 2024 - Takeda announced the FDA approval of Iclusig (ponatinib), in combination with chemotherapy, for treatment of adult patients with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL)

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Without a loading phase, muscle creatine stores reach full saturation in approximately 3-4 weeks of daily 5-gram dosing

Its clinical program spans over 25,000 participants across the SUSTAIN, PIONEER, STEP, and SELECT trial programs