NeOnc_Technologies
Sep 30, 2:35 PM
November 17 marks the next regulatory milestone for
$NTHI.
Following completion of NEO212 Phase 1 dose escalation and selection of 610 mg as the recommended Phase 2 dose, we have scheduled an in-person End-of-Phase 1 Type B Meeting with the FDA.
The meeting will focus on patient population, trial design, endpoints and the evidence needed to support NEO212’s next stage of development, while also seeking FDA feedback on a potential registrational strategy and accelerated approval pathway.
$NTHI $VKTX $MRNA
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