For years, they’ve been working on a real-world problem that still eludes Big Pharma. And now they may have one of the most exciting biologics in development.
They are the biotech disruptor, Cytonics. After successfully treating 10,000+ osteoarthritis patients with their first-generation OA therapy, Cytonics is pioneering a next-gen treatment: CYT-108. A genetically-engineered variant of the naturally-occurring Alpha-2-Macroglobulin protein, CYT-108 could become one of the first disease-modifying drugs for OA.
CYT-108 recently completed FDA Phase 1 clinical trials — but there’s more. Recent research suggests that CYT-108's "super A2M" activity may prove to be potent as a melanoma therapy. With a provisional U.S. patent filed to expand the drug into oncology, Cytonics is rapidly evolving into the next potential biotech breakthrough.