• TRADE NAME: Ayvakit (Blueprint Medicines)
  • INDICATIONS: Treatment of adults with unresectable or metastatic gastrointestinal stromal tumor harboring a platelet-derived growth factor receptor alpha (PDGFRA) exon 18 mutation, including PDGFRA D842V mutations.
  • CLASS: Tyrosine kinase inhibitor
  • HALF-LIFE: 32–57 hours
  • FDA APPROVAL DATE: 01/09/2020
  • CLINICALLY IMPORTANT, POTENTIALLY HAZARDOUS INTERACTIONS WITH:
    CYP3A inducer, CYP3A inhibitor, Efavirenz, Fluconazole, Itraconazole
  • PREGNANCY: Can cause fetal harm. Advise females of reproductive potential of the potential risk to a fetus and to use effective contraception.

Intracranial Hemorrhage: Withhold avapritinib for grade 1 or 2 reactions (subdural hematoma, intracranial hemorrhage, and cerebral hemorrhage) until resolution and then resume at a reduced dose. Permanently discontinue for recurrent grade 1 or 2 reactions or first occurrence of grade 3 or 4 reactions.

Please login to view the rest of this drug profile.

Page last updated 09/23/2024

Symbol key

Incidence

<1% 1‑5% 5‑10% 10‑15% 15‑20% 20‑30% >30%

Seriousness

Hospitalization possible
Life threatening
Fatal

Warnings in other populations

BreastfeedingBreast feeding

GeriatricGeriatric

PediatricPediatric