U.S. FDA approval ahead of Veyonda Phase 1b study

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    Noxopharm (ASX:NOX) receives approval from U.S. FDA for Veyonda



    • Clinical drug development company Noxopharm (NOX) has received approval from the U.S. Food and Drug Administration for its Veyonda cancer treatment
    • This approval will see Noxopharm begin a study in using Veyonda to treat cancerous cells found in fat, blood and muscle tissue
    • Chief Medical Officer Gisela Mautner said the drug met the FDA's very high standard as a safe and well-tolerated drug

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