41
Participants
Start Date
September 30, 2025
Primary Completion Date
September 30, 2027
Study Completion Date
December 31, 2027
OPM-101
"OPM-101 will be administered in combination with an authorized regimen of Pembrolizumab.~Pembrolizumab will be administered by IV infusion either at a dose of 200 mg every 3 weeks or at a dose of 400 mg every 6 weeks, as per Principal Investigator's decision."
Lead Sponsor
Oncodesign Precision Medicine
INDUSTRY