FDA OKays Proceeding with Phase 1/2 Trials of NEO212 for Primary Brain Tumors and for Brain Metastasis in Combination with Standard of Care Therapy
“We believe receiving this authorization from the FDA will enable us to advance NEO212 into the clinic where we believe it can have a positive effect on treatment outcomes,” stated NeOnc CEO, Thomas Chen, MD, Ph.D. “Based on pre-clinical testing, we believe NEO212 may be effectively delivered to the brain to treat primary brain tumors.”
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