NCT02744287

A Phase 1/2 Feasibility, Safety, and Activity Study of PSCA-Specific Chimeric Antigen Receptor Engineered T Cells (BPX-601) in Subjects With Previously Treated Advanced Solid Tumors

Study Summary

The purpose of this study is to evaluate the safety and activity of BPX-601 CAR-T cells in participants with previously treated advanced solid tumors (prostate) expressing high levels of prostate stem cell antigen (PSCA). Participants' T cells are modified to recognize and target the PSCA tumor marker on cancer cells.

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Interventions

BPX-601BIOLOGICAL
Autologous T cells genetically modified with retrovirus vector containing PSCA-specific CAR and an inducible MyD88/Cluster Designation (CD)40 (iMC) co-stimulatory domain
RimiducidDRUG
Dimerizer infusion to activate the iMC of the BPX-601 cells for improved proliferation and persistence

Study Locations

FacilityCityStateCountry
Moffitt Cancer CenterTampaFloridaUnited States
Emory Winship Cancer InstituteAtlantaGeorgiaUnited States
Rush University Medical CenterChicagoIllinoisUnited States
University of Chicago MedicineChicagoIllinoisUnited States
Karmanos Cancer InstituteDetroitMichiganUnited States
University of NebraskaOmahaNebraskaUnited States
John Theurer Cancer Center, Hackensack University Medical CenterHackensackNew JerseyUnited States
Roswell Park Cancer InstituteBuffaloNew YorkUnited States
Columbia University Medical CenterNew YorkNew YorkUnited States
Duke UniversityDurhamNorth CarolinaUnited States
Thomas Jefferson UniversityPhiladelphiaPennsylvaniaUnited States
Baylor Sammons Cancer CenterDallasTexasUnited States
The University of Texas MD Anderson Cancer CenterHoustonTexasUnited States

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: April 14, 2026