- Calidi partnered with Avance Clinical to support Australian regulatory approval and accelerate initiation of first-in-human clinical trials for CLD-401 in Australia.
- The collaboration is intended to facilitate clinical trial initiation in Australia while Calidi pursues an FDA IND filing in 2026.
- CLD-401 is a genetically modified vaccinia virus designed to replicate only in tumor cells and express an IL-15 superagonist in the tumor microenvironment.
- The planned phase I trial will evaluate safety and pharmacodynamics in patients with solid tumors.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Calidi Biotherapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603240800PRIMZONEFULLFEED9677135) on March 24, 2026, and is solely responsible for the information contained therein.
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