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Saniona completed toxicology and CMC work for SAN2465, clearing the package needed to support an IND filing. IND submission to the FDA is targeted by end-October 2026, setting up first-in-human dosing plans. Planned Phase 1 trial targets safety, tolerability, pharmacokinetics in healthy volunteers, with biomarker reado
Saniona completed required toxicology and CMC work for SAN2465, clearing the way for a US IND filing by end-October 2026. The company is finalizing IND documentation for submission to the FDA. A planned Phase 1 trial would test safety, tolerability, pharmacokinetics, and biomarkers in healthy volunteers. Disclaimer: Th