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Tikva Allocell Secures $8 Million to Advance Solid Tumor Therapy

With $8 million in Series A funding led by Kantharos Capital, Singapore-based Tikva Allocell is moving its lead candidate, TAVST01, toward a 2026 clinical trial. The firm aims to solve the persistent rejection issues that have historically hindered donor-derived cell therapies in the treatment of solid tumors.

Tikva Allocell Secures $8 Million to Advance Solid Tumor Therapy

The capital injection will support IND-enabling activities and a planned year-end IND submission for TAVST01, a therapy designed to target B7-H3 proteins found in lung, breast, prostate, and pancreatic cancers. Unlike conventional treatments that are often cleared by the patient's immune system, TAVST01 utilizes Epstein-Barr virus-specific T cells, which the body naturally sustains, to ensure greater durability and persistence.

Tikva’s technology, licensed from Baylor College of Medicine, employs an ALLO SerpinB9 EBVST platform. By integrating an optimized form of SerpinB9—a natural inhibitor of granzyme B—the therapy provides a protective 'armor' that allows donor cells to resist rejection while minimizing the risk of graft-versus-host disease. Dr. Ivan Horak, CEO of Tikva Allocell, noted that this approach addresses the primary barriers in solid-tumor treatment by requiring minimal gene editing while maintaining a robust anti-tumor response. The company plans to initiate Phase 1 trials in Singapore and the United States, targeting patients who currently face limited treatment options.

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