15
Participants
Start Date
September 20, 2021
Primary Completion Date
November 13, 2023
Study Completion Date
November 13, 2023
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.
UPMC Hillman Cancer Center, Pittsburgh
Collaborators (2)
Agios Pharmaceuticals, Inc.
INDUSTRY
Bristol-Myers Squibb
INDUSTRY
Jason J. Luke, MD
OTHER