SARC038: Phase 2 Study of Regorafenib and Nivolumab in Osteosarcoma

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

June 4, 2021

Primary Completion Date

May 31, 2025

Study Completion Date

June 30, 2026

Conditions
OsteosarcomaOsteosarcoma in ChildrenOsteosarcoma RecurrentOsteosarcoma Metastatic
Interventions
DRUG

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.

DRUG

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.

DRUG

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."

Trial Locations (8)

21287

Johns Hopkins, Baltimore

33136

University of Miami, Miami

45229

Cincinnati Children's, Cincinnati

48109

University of Michigan, Ann Arbor

55455

University of Minnesota, Minneapolis

75390

UT Southwestern Medical Center, Dallas

90027

Children's Hospital of Los Angeles, Los Angeles

97239

Oregon Health and Sciences University, Portland

All Listed Sponsors
lead

Sarcoma Alliance for Research through Collaboration

OTHER