Ivosidenib (AG-120) With Nivolumab in IDH1 Mutant Tumors

PHASE2CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

September 20, 2021

Primary Completion Date

November 13, 2023

Study Completion Date

November 13, 2023

Conditions
Advanced Solid TumorIDH1 MutationGlioma
Interventions
DRUG

ivosidenib and nivolumab

Ivosidenib will be administered orally at a dose of 500 mg (provided as 250 mg strength tablets) daily. The dose may be reduced to 250 mg for patients experiencing more than one event of Grade 2 nausea or vomiting (related or unrelated), or Grade 3 or Grade 4 adverse events. Nivolumab will be administered at 480 mg IV every 28 days.

Trial Locations (1)

15232

UPMC Hillman Cancer Center, Pittsburgh

All Listed Sponsors
collaborator

Agios Pharmaceuticals, Inc.

INDUSTRY

collaborator

Bristol-Myers Squibb

INDUSTRY

lead

Jason J. Luke, MD

OTHER