• NEC Bio Therapeutics' NECVAX-NEO1, combined with checkpoint inhibitors, demonstrates encouraging interim results in a Phase 1 trial for solid tumors.
• The personalized, bacteria-based oral DNA vaccine induced an ELISPOT response in 68% of neoepitopes, with 40% of patients showing significant neoantigen-specific signals.
• After 24 weeks, 80% of patients treated with NECVAX-NEO1 achieved stable disease status, indicating a high disease control rate in melanoma, renal cell, and head and neck cancer patients.
• The Phase 1 trial showed no treatment-related toxicities, supporting further investigation of NECVAX-NEO1 as a potential treatment option for difficult-to-treat cancers.