NMPA granted Priority Review Status to Geptanolimab

On August 5, 2020 Genor Biopharma Co. Inc reported that National Medical Products Administration (NMPA) has granted priority review status to its new drug application (NDA) for Geptanolimab, a PD-1 mAb, on July 28, 7 days after the NDA acceptance (Press release, Genor Biopharma, AUG 5, 2020, View Source [SID1234594762]).

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Relapsed/refractory Peripheral T cell Lymphoma (PTCL) is the first indication that Genor targeted for its Geptanolimab. It is currently the first PD-1 mAb in China and globally being applied for this disease setting.