48
Participants
Start Date
June 4, 2021
Primary Completion Date
May 31, 2025
Study Completion Date
June 30, 2026
Regorafenib 40 MG
For subjects age 18 and older, Regorafenib will be administered as 80mg oral once daily on Cycle 1, Days 1-7 and then escalated to 120 mg once daily for Cycle 1, Days 8-21 if no Grade 2 or above regorafenib adverse events occur. For subsequent cycles, the highest tolerated dose will be taken once daily on days 1-21 of each 28-day cycle.
Regorafenib 20MG
For subjects younger than 18 years, Regorafenib will be administered as 60mg/m2/dose (rounded to the nearest 20mg, maximum dose of 80mg) once daily for Cycle 1, Days 8-21 if no Grade 2 or above regorafenib-related adverse events occur. For subsequent cycles, the highest tolerated dose will be taken once daily on days 1-21 of each 28-day cycle.
Nivolumab
"For subjects age 18 and older, Nivolumab will be administered at 480mg IV over 30 min every 28 days.~For subjects younger than 18 years, Nivolumab 3mg/kg (maximum dose 240mg) will be administered IV over 30 minutes on day 1 and 15 of each 28-day cycle."
Johns Hopkins, Baltimore
University of Miami, Miami
Cincinnati Children's, Cincinnati
University of Michigan, Ann Arbor
University of Minnesota, Minneapolis
UT Southwestern Medical Center, Dallas
Children's Hospital of Los Angeles, Los Angeles
Oregon Health and Sciences University, Portland
Sarcoma Alliance for Research through Collaboration
OTHER