Cellular Biomedicine Group Announces FDA Clearance of IND Application for Novel TIL Therapy C-TIL051

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Cellular Biomedicine Group Inc. (CBMG or the “Company”), a biopharmaceutical company developing innovative cellular immunotherapies for the treatment of cancer, today announced that the Food and Drug Administration (FDA) granted clearance of the Investigational New Drug (IND) application to proceed with Phase 1 clinical development of its novel Tumor Infiltrating Lymphocyte (TIL) product C-TIL051 for late-stage Non-Small Cell Lung Cancer (NSCLC) patients that are relapsed or refractory to anti-PD1 therapy.