64
Participants
Start Date
January 14, 2019
Primary Completion Date
June 30, 2026
Study Completion Date
June 30, 2026
GP-2250
GP-2250 monotherapy for pharmacokinetics and safety; GP-2250 plus gemcitabine for safety, tolerability, pharmacokinetics, and biomarker assessments
Abramson Cancer Center at the University of Pennsylvania, Phildelphia
Wake Forest Baptist Health, Winston-Salem
University of Kansas Cancer Center, Fairway
Hoag Family Cancer Institute, Newport Beach
Beth Israel Deaconess Medical Center, Boston
Lead Sponsor
Translational Drug Development
OTHER
Geistlich Pharma AG
INDUSTRY