A Phase 1 Study Evaluating DISP-10 in Participants With Advanced Gastrointestinal Cancers
Start Date
4/1/2026
Completion Date
4/1/2046
Summary
This is a Phase 1, multicenter, open-label study of DISP-10, a combination therapy consisting of DV-10 (adenovirus) and idecabtagene vicleucel (ide-cel, BCMA-directed chimeric antigen receptor \[CAR\] T), in adult participants with advanced gastrointestinal (GI) cancers. The study will consist of 2 parts: dose-escalation (Part 1) and dose-expansion (Part 2). Part 1 of the study will evaluate the safety and tolerability of increasing dose levels of DISP-10 to establish the recommended dose for expansion (RDE); Part 2 will evaluate the safety and efficacy of DISP-10 in participants treated at the RDE.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
DISP-10
Conditions
Locations
City of Hope
Duarte, California 91010
United States
University of Cincinnati Cancer Center
Cincinnati, Ohio 45267
United States
Tennessee Oncology
Nashville, Tennessee 37203
United States