NeOnc Initiates Cohort 3 in Phase 1 Clinical Trial of NEO212™, a Patented Novel Hybrid Drug Designed to Deliver ‘Double Punch’ Against Malignant Brain Tumors
The NEO™ technology platform enables novel drug production via bioconjugation and unique delivery methods designed to address the persistent challenges with overcoming the blood-brain barrier.WESTLAKE VILLAGE, Calif., July 24, 2024 (GLOBE NEWSWIRE) -- NeOnc Technologies Holdings, Inc., a clinical-stage medical biotechnology company, has begun enrollment of patients for Cohort 3 out of 6 of the Phase 1 clinical trial of NEO212™, the company’s patented novel hybrid drug designed to deliver a double punch’ against primary and secondary malignant brain tumors.
Chen and his medical and scientific teams. The NEO212 clinical trial is titled, Open-Label, Phase 1/2 Dose Finding, Safety and Efficacy Study of Oral NEO212 in Patients with Astrocytoma IDH-Mutant, Glioblastoma IDH-Wildtype or Uncontrolled Metastasis to the Brain in Patients with Select Solid Tumors.’ The company recently announced that its Phase 2a clinical trial of NEO100-01™, titled, 'An Open-Label, Phase 1/2a Dose Escalation Study of Safety and Efficacy of NEO100 in Recurrent Grade IV Glioma,’ was expanded from Grade IV to Grade III Astrocytoma with IDH1 mutation.
"Now that we are nearly halfway through our Phase 1 clinical trial of NEO212, we are encouraged that NEO212 may eventually impact the standard of care for primary brain tumors and other cancers that can spread to the brain,” commented NeOnc CEO, Thomas Chen, MD, Ph.D.
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Author / Journalist: NeOnc Technologies Holdings, Inc.
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