SOTIO Presents Overview of DUET-01 Phase 1/2 Study at ASCO Annual Meeting

On May 23, 2024 SOTIO Biotech, a clinical-stage immuno-oncology company owned by PPF Group, reported that it will present on June 1, 2024 (Developmental Therapeutics—Immunotherapy session) a Trial-in-Progress poster on the first-in-human DUET-01 Phase 1/2 study at the 2024 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting (Press release, SOTIO, MAY 23, 2024, View Source [SID1234643658]). The study is evaluating the use of BOXR1030, a metabolically enhanced CAR T-cell therapy, for the treatment of patients with solid tumors.

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!

Patient enrollment and dosing in the DUET-01 clinical trial (NCT05120271) are ongoing at three leading cancer care centers across the U.S., with additional sites expected to be imminently initiated in the U.K.

"The arrival of CAR T-cell therapies has profoundly improved the therapeutic outlook for patients with some blood cancers. Unfortunately, the same has not been true for solid tumors, where cell therapies’ success has been stymied by the challenges of overcoming the tumor microenvironment," said Ecaterina Dumbrava, M.D., Assistant Professor of Investigational Cancer Therapeutics at The University of Texas MD Anderson Cancer Center and primary investigator on the DUET-01 trial. "As a metabolically enhanced GPC3-targeting CAR T-cell therapy, BOXR1030 has shown promising preclinical results in resisting tumor microenvironment-like conditions and improving T cell proliferation compared with standard CAR T cells. GPC3 is a clinically validated tumor-restricted target with a high prevalence in several solid tumor indications with unmet medical need. Given these promising observations thus far, we are looking forward to continuing to evaluate its potential in a clinical setting in the DUET-01 study."

The DUET-01 clinical trial is a first-in-human, open-label, multicenter, dose escalation study to assess and determine the recommended Phase 2 dose of BOXR1030 in patients with GPC3-positive advanced solid tumors. The trial will enroll up to 98 patients with advanced, unresectable hepatocellular carcinoma, squamous cell lung cancer, myxoid/round cell liposarcoma, and Merkel cell carcinoma.

Presentation materials will be available on June 1, after presentations conclude, here.