NeOnc_Technologies
NEO212 enters its next regulatory milestone with Phase 1 dose escalation completed and 610 mg selected as the recommended Phase 2 dose.
Clinical observations reported to date include approximately 60% tumor reduction followed by 21 months of disease control in one recurrent GBM patient, and approximately 16 months of stable disease in a patient with brain metastases.
While individual cases do not establish efficacy, these observations provide important clinical context as we prepare for the November 17 FDA meeting and the next stage of NEO212’s development.
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