Vorasidenib is an oral cancer drug sold under the brand name Voranigo that inhibits mutated forms of the enzymes isocitrate dehydrogenase 1 and 2. Tumor cells carrying a mutation in either enzyme produce an abnormal metabolite called 2 hydroxyglutarate that drives malignant growth, and vorasidenib blocks both mutated forms at once, letting affected cells differentiate normally and slowing their growth. Servier Laboratories brought the drug to approval, and the United States Food and Drug Administration cleared it in August 2024 for adults and children twelve and older with grade 2 astrocytoma or oligodendroglioma carrying a susceptible IDH1 or IDH2 mutation who have already had surgery. It was the first FDA approved systemic therapy for that specific patient group. Vorasidenib is taken as a 40 milligram tablet once a day, giving patients with these slow growing brain tumors an oral option after surgery rather than immediate chemotherapy or radiation.
Facts
Classification
Approval Status ATC ClassSourced to the subject's own accountL: Antineoplastic and Immunomodulating Agents 2 Route of Administration First Approved / Isolated Year Connections
Sources
1. Vorasidenib (Wikipedia)
Lead section, approval-status statementQuote, Lead section, approval-status statement
Vorasidenib was approved for medical use in the United States in August 2024.
View the Source 2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code LQuote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source 3. Vorasidenib (Wikipedia)
WikipediaInfobox drug, routes_of_administrationQuote, Infobox drug, routes_of_administration
By mouth
View the Source 4. Drugs.com: Voranigo (vorasidenib) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Voranigo (vorasidenib) was first approved by the FDA on August 6, 2024
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