Agios receives nod for ivosidenib

July 23, 2018 | Monday | News

Orphan Drug-tagged ivosidenib, an orally available IDH1 inhibitor, had Fast Track status.

Singapore – The FDA approves Agios Pharmaceuticals' TIBSOVO (ivosidenib) for the treatment of adult patients with relapsed/refractory acute myeloid leukemia (AML) with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation.

Orphan Drug-tagged ivosidenib, an orally available IDH1 inhibitor, had Fast Track status.

 

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