
Pharmaceutical R&D Developer
The Center for Drug Evaluation (CDE) of China's National Medical Products Administration (NMPA) announced that the new indication marketing authorization application for dupilumab injection (dupilumab, English trade name: Dupixent) submitted by Sanofi in China has been proposed for priority review by the CDE. The proposed indication is: for the treatment of moderate-to-severe atopic dermatitis in adults and pediatric patients aged 6 to less than 12 years who are inadequately controlled by or for whom topical prescription therapies are not recommended.