Cadonilimab Receives Regulatory Approval from China's NMPA for First-Line Treatment of Advanced Cervical Cancer, Reports Akeso Inc

Reuters
06-16
Cadonilimab Receives Regulatory Approval from China's NMPA for First-Line Treatment of Advanced Cervical Cancer, Reports Akeso Inc

Akeso Inc. has announced a significant regulatory approval for their innovative treatment, cadonilimab. The China National Medical Products Administration (NMPA) has approved the use of cadonilimab as a first-line treatment for advanced, recurrent, or metastatic cervical cancer as of May 2025. This approval marks an important milestone for Akeso, as cadonilimab, a first-in-class PD-1/CTLA-4 bispecific antibody, has shown significant improvements in progression-free survival and overall survival in various patient subgroups. This development highlights the ongoing impact of cadonilimab in transforming the treatment standards for advanced cervical cancer and underscores its potential global health benefits for women.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Akeso Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: CN10670) on June 16, 2025, and is solely responsible for the information contained therein.

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