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Ivosidenib

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This is an old revision of this page, as edited by 213.120.141.2 (talk) at 16:12, 14 August 2018 (updated that the drug is now FDA approved). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Ivosidenib
Clinical data
Routes of
administration
Oral
ATC code
  • None
Legal status
Legal status
Identifiers
  • (2S)-N-{(1S)-1-(2-chlorophenyl)-2-[(3,3- difluorocyclobutyl)amino]-2-oxoethyl}-1-(4-cyanopyridin2-yl)-N-(5-fluoropyridin-3-yl)-5-oxopyrrolidine2-carboxamide
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC28H22ClF3N6O3
Molar mass582.97 g·mol−1
3D model (JSmol)
  • C1CC(=O)N([C@@H]1C(=O)N(C2=CC(=CN=C2)F)[C@@H](C3=CC=CC=C3Cl)C(=O)NC4CC(C4)(F)F)C5=NC=CC(=C5)C#N

Ivosidenib is an experimental drug for treatment of cancer. It is a small molecule inhibitor of IDH1, which is mutated in several forms of cancer. The drug is being developed by Agios Pharmaceuticals and is in phase III clinical trials. The FDA awarded orphan drug status for acute myeloid leukemia and cholangiocarcinoma.[2][better source needed]

Ivosidenib was approved by the FDA for acute myeloid leukemia (AML) with an IDH1 mutation and is presently in a phase III clinical trial for cholangiocarcinoma with an IDH1 mutation.[3] Ivosidenib was the first anticancer therapy to approved for patients with a specific genetic variant (citation needed).

References

  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
  2. ^ http://adisinsight.springer.com/drugs/800040155
  3. ^ Study of AG-120 (Ivosidenib) vs. Placebo in Combination With Azacitidine in Patients With Previously Untreated Acute Myeloid Leukemia With an IDH1 Mutation (AGILE)