NMPA accepts NDA for sevabertinib (BAY 2927088) for previously treated NSCLC patients with HER2/ERBB2 mutations
“The acceptance for review of sevabertinib by the Center for Drug Evaluation in China is a significant milestone that validates our ongoing efforts to develop personalized healthcare solutions that help people living with cancer,” said Christine Roth, Executive Vice President, Global Product Strategy and Commercialization and Member of the Pharmaceuticals Leadership Team at Bayer. “If approved, sevabertinib will help address critical unmet challenges and improve outcomes for these patients, who currently have a poor prognosis and limited treatment options.”
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