Arsenal Biosciences Announces First Patient Dosed in Phase 1/2 Clinical Trial of AB-2100 in Development as a Treatment for Clear-cell Renal Cell Carcinoma

On April 30, 2024 Arsenal Biosciences, Inc. (ArsenalBio), a clinical stage programmable cell therapy company focused on engineering advanced CAR T-cell therapies for solid tumors, reported that the first patient has been dosed with AB-2100 in a multi-center, open-label Phase 1/2 clinical trial for patients with clear-cell renal cell carcinoma (ccRCC) (Press release, ArsenalBio, APR 30, 2024, View Source [SID1234642488]). AB-2100 utilizes ArsenalBio’s CITE (CRISPR Integration of Transgenes by Electroporation) technology to engineer T cells to selectively target the tumor and overcome the suppressive tumor microenvironment. These engineering features will potentially enable the patient’s immune system to destroy ccRCC cells without harming normal tissues.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

"Kidney cancer is an immunologically responsive malignancy with several FDA approved immunotherapies on the market. But despite much progress in the field, there remains a tremendous unmet need in this indication, which we believe our Integrated Circuit T (ICT) cell technology is ideally suited to address," said Susie Jun, M.D., Ph.D., ArsenalBio’s Chief Medical Officer. "As with our AB-1015 program in ovarian cancer, we hope this study succeeds in identifying a safe and therapeutic dose to enable further study of this potential therapy in larger patient cohorts."

The Phase 1/2 trial (NCT06245915 ) is a dose escalation study that will evaluate the safety and efficacy of AB-2100 in patients with ccRCC that either came back or did not improve after treatment with a checkpoint inhibitor and a VEGF inhibitor. The goal of the study is to determine the maximum tolerated dose of AB-2100, which is administered intravenously via a single infusion following completion of conditioning chemotherapy. The study is expected to enroll up to 60 patients in Phase 1 and 130 patients total across multiple clinical sites in the United States.

AB-2100 is an ICT cell therapy engineered with the intent to treat ccRCC. The foundational manufacturing technique is precise and specific CRISPR-mediated insertion of a large synthetic double-stranded DNA cassette into a novel safe harbor site in Chromosome 11. The cassette encodes several features: a synthetic logic gate designed to optimize how the ICT cells target tumors and avoid normal tissues by requiring the presence of two distinct proteins in ccRCC (prostate-specific membrane antigen (PSMA) on tumor endothelium and carbonic anhydrase 9 (CA9) on the adjacent tumor cell); shRNAs to armor the T cell against immunosuppressive signals in the TME; and a novel synthetic pathway activator (SPA) designed to increase the potency and functional persistence of the engineered T cells.

"Our logic gate approach was designed to selectively target tumors and spare normal tissues by requiring the presence of two antigens in close proximity," said Dr. Jun. "Based upon our preclinical data we believe this synthetic biology-based logic gate approach will enable targeting of antigens like CA9 where conventional CAR T-cell strategies have been limited by on-target toxicity in healthy tissues."

AB-2100 is ArsenalBio’s second internally discovered T cell therapeutic candidate to enter clinical development. A multi-center, open-label phase 1 dose escalation trial (NCT05617755) of AB-1015, under investigation for the treatment of ovarian cancer, is currently enrolling.