FDA Approves Ivosidenib in IDH1-Mutated MDS
Ivosidenib monotherapy is now approved by the FDA for patients with relapsed/refractory myelodysplastic syndrome with an IDH1 mutation.
Stay updated with breaking news from Abbott Realtime. Get real-time updates on events, politics, business, and more. Visit us for reliable news and exclusive interviews.
Ivosidenib monotherapy is now approved by the FDA for patients with relapsed/refractory myelodysplastic syndrome with an IDH1 mutation.
The FDA approval was based on a small study, in which 38.9% of patients with relapsed or refractory disease went into complete remission.
The FDA has approved Tibsovo (ivosidenib) for the treatment of adults with relapsed or refractory MDS with a susceptible IDH1 mutation.
/PRNewswire/ -- Today, the U.S. Food and Drug Administration approved Tibsovo (ivosidenib) for the treatment of adult patients with relapsed or refractory...
The Food and Drug Administration approved Tibsovo for patients with relapsed or refractory myelodysplastic syndromes with a susceptible isocitrate dehydrogenase-1 mutation.