On March 7, 2024 Verismo Therapeutics, a clinical-stage CAR-T company developing the novel KIR-CAR platform technology, reported that it has activated a second clinical site for its STAR-101 Phase 1 clinical trial at The University of Texas MD Anderson Cancer Center (Press release, Verismo Therapeutics, MAR 7, 2024, View Source [SID1234640943]).
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STAR-101 is a multi-center clinical trial designed to evaluate Verismo Therapeutic’s lead candidate, SynKIR-110, for the treatment of mesothelin-overexpressing ovarian cancer, malignant pleural mesothelioma, and cholangiocarcinoma.
"This milestone marks the steady progress towards our goal of bringing SynKIR-110 to as many patients as possible," said Dr. Bryan Kim, Co-Founder and CEO of Verismo Therapeutics. "We are grateful for the opportunity to work with Dr. Mehmet Altan at MD Anderson to bring us closer to that goal."
Verismo achieved clearance from the FDA to initiate this multi-center clinical trial for SynKIR-110 and has partnered with the Hospital of the University of Pennsylvania as the first clinical site.
Verismo has previously announced that SynKIR-110 received Orphan Drug Designation and Fast Track Designation for the treatment of mesothelin-expressing mesotheliomas.
For more information about the STAR-101 clinical trial, please visit ClinicalTrials.gov NCT05568680.
About the KIR-CAR Platform
The KIR-CAR platform is a dual-chain CAR T cell therapy and has been shown in preclinical animal models to be capable of maintaining antitumor T cell activity even in challenging solid tumor environments. DAP12 acts as a novel costimulatory molecule for T cells using additional T cell stimulating pathways, further sustaining chimeric receptor expression and improving KIR-CAR T cell functional persistence. This continued T cell function and persistence can lead to ongoing regression of solid tumors in preclinical models, including those resistant to traditional CAR T cell therapies. The KIR-CAR platform is being investigated in combination with many additional emerging technologies, such as in vivo gene engineering, advanced cell manufacturing and reprogramming, combinational therapies, and even allogeneic cellular therapies to potentially provide the next-generation multimodal targeted immunotherapy for patients in need.