Regulatory approval

Published by the Food and Drug Administration. Approved

TIBSOVO is an isocitrate dehydrogenase-1 (IDH1) inhibitor indicated for patients with a susceptible IDH1 mutation as detected by an FDA-approved test with for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma who have been previously treated.

This is written in the approval document.

Citation

Agios Pharmaceuticals, Inc. Tibsovo (ivosidenib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211192s011lbl.pdf. Revised October 2023. Accessed October 30, 2024.

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Therapeutic response

Precision oncology relationships for therapeutic response derived from this regulatory approval.

Organizations Biomarkers Cancer types Therapies
FDA (1) IDH1 p.R132C Cholangiocarcinoma Ivosidenib
FDA (1) IDH1 p.R132G Cholangiocarcinoma Ivosidenib
FDA (1) IDH1 p.R132H Cholangiocarcinoma Ivosidenib
FDA (1) IDH1 p.R132L Cholangiocarcinoma Ivosidenib
FDA (1) IDH1 p.R132S Cholangiocarcinoma Ivosidenib