NeOnc gets FDA manufacturing feedback for NEO212 tablet transition

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NeOnc Receives FDA Written Feedback on NEO212 CMC Development and Capsule-to-Tablet Transition

July 15, 2026 9:00 AM EDT

FDA feedback provides detailed manufacturing and formulation requirements for continued late-stage development of NEO212

CALABASAS, Calif., July 15, 2026 (GLOBE NEWSWIRE) -- NeOnc Technologies Holdings, Inc. (NASDAQ: NTHI) (NeOnc or the Company), a clinical-stage life sciences company focused on the development of treatments for central nervous system cancers, today announced that it has received written feedback from the U.S. Food and Drug Administration (FDA) regarding the chemistry, manufacturing and controls (CMC) development program for NEO212, the Companys novel temozolomide-perillyl alcohol conjugate.

The written feedback was provided in advance of a Type B End-of-Phase... More