This is a multi-center, open-label phase 1/2 trial evaluating the safety and efficacy of
AB-2100 cell product. The study may enroll approximately 60 patients in phase 1 and
approximately 70 patients in phase 2.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06245915.
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 the patients who have been diagnosed with clear-cell renal
cell carcinoma that either came back or did not improve after treatment with a checkpoint
inhibitor and a VEGF inhibitor. The purpose of this study is to test the safety and
efficacy of AB-2100 cells in patients with renal cell carcinoma. This treatment has not
been approved by the Food and Drug Administration.
The goal of this study is to determine the maximum tolerated dose of the AB-2100 cells. 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 patient and will have a
genetic circuit/logic gate put in them that makes them able to recognize
prostate-specific membrane antigen (PSMA) and carbonic anhydrase 9 (CA9), 2 proteins
found on 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-2100 cells are given as a single intravenous infusion. Patients may be assigned to
receive conditioning chemotherapy prior to the infusion
After completion of study treatment, patients 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 OrganizationArsenal Biosciences, Inc.