Cellular Biomedicine Group Inc. 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. C-TIL051 is an autologous adoptive cell therapy comprised of a patient's ex vivo expanded lymphocytes using CBMG's proprietary manufacturing process.