51
Participants
Start Date
October 15, 2021
Primary Completion Date
February 1, 2024
Study Completion Date
June 19, 2025
S095029
S095029 will be administered via IV infusion every 2 weeks. Once the DLT evaluations period at the second dose level is completed and it is deemed as safe, the dose escalation part 1b will be initiated.
S95029 and Sym021
Sym021 will be administered at a fixed dose of 200mg. S095029 will be administered via IV infusion every 2 weeks. Once the RP2D dose of S95029 in combination with Sym21 is defined, dose expansion will begin.
START Midwest, Grand Rapids
Mary Crowley Cancer Research, Dallas
The University of Texas MD Anderson Cancer Center, Houston
The START Center for Cancer Care, San Antonio
Princess Margaret Cancer Centre, Toronto
ADIR, a Servier Group company
INDUSTRY
Institut de Recherches Internationales Servier
OTHER