drugset / Trial / NCT04164901

Study of Vorasidenib (AG-881) in Participants With Residual or Recurrent Grade 2 Glioma With an IDH1 or IDH2 Mutation (INDIGO)

NCT04164901 ↗

Phase 3 Active not recruiting 331 enrolled Servier
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Study AG881-C-004 is a phase 3, multicenter, randomized, double-blind, placebo-controlled study comparing the efficacy of vorasidenib to placebo in participants with residual or recurrent Grade 2 glioma with an IDH1 or IDH2 mutation who have undergone surgery as their only treatment. Participants will be required to have central confirmation of IDH mutation status prior to randomization. Approximately 340 participants are planned to be randomized 1:1 to receive orally administered vorasidenib 40 mg QD or placebo.

Timeline

Start
2020-01-05
Primary completion
2022-09-06
Completion
2028-05

Outcome

Met primary endpoint

registry analysis (superiority test); Vorasidenib vs Matching Placebo; p <0.0000001; Cox Proportional Hazard 0.39 (95% CI 0.27 to 0.56); Kaplan-Meier NCT04164901 ↗

registry MEDIAN Vorasidenib: 27.7 (17.0 to NA) months MEDIAN Matching Placebo: 11.1 (11.0 to 13.7) months NCT04164901 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Vorasidenib Small molecule 40 mg Oral

Indications