
NeOnc Technologies said the FDA provided written feedback outlining detailed manufacturing and formulation requirements to support continued late-stage development of its NEO212 program. The update is procedural and does not include efficacy or commercial milestones, implying limited near-term financial impact.
NeOnc Technologies said the FDA provided written feedback outlining detailed manufacturing and formulation requirements to support continued late-stage development of its NEO212 program. The update is procedural and does not include efficacy or commercial milestones, implying limited near-term financial impact.
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