This is a multi-center, open-label Phase 1/2 trial evaluating the safety and efficacy of
AB-3028 in subjects with metastatic castration resistant prostate cancer (mCRPC).
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07285694.
Locations matching your search criteria
United States
Iowa
Iowa City
University of Iowa/Holden Comprehensive Cancer CenterStatus: Active
Name Not Available
This study is intended for subjects diagnosed with metastatic castration-resistant
prostate cancer (mCRPC) and whose disease progressed after treatment with an androgen
receptor pathway inhibitor (ARPI). The purpose of this study is to test the safety and
efficacy of AB-3028 cells in subjects with metastatic castration-resistant prostate
cancer. This treatment has not been approved by the Food and Drug Administration.
The goal of the Phase I portion of this study is to evaluate safety profile of AB-3028
and to determine the maximum tolerated dose or recommended phase 2 dose of AB-3028. The
Phase 2 portion of the study will investigate the efficacy of AB-3028. T cells are part
of the immune system that protect the body from infection and may help fight cancer. The
T cells given in this study will come from the subject and will have a DNA cassette put
in them that makes them able to recognize a priming antigen as well as Prostate-Specific
Membrane Antigen (PSMA), two proteins found on prostate cancer tumor cells. These
logic-gated T cells may help the body's immune system identify and kill cancer cells
while sparing normal healthy tissues from toxicity.
The AB-3028 cells are given as a single intravenous infusion.
After completion of study treatment, subjects are followed with serial measurements of
safety, tolerability and response.
This is a research study to obtain new information that may help people in the future.
Lead OrganizationArsenalBio Inc