The FDA has accepted Sanofi and Regeneron’s application to expand Dupixent’s use, with a decision expected by April 2025.
Microbion has reported positive topline results from its Phase II study of pravibismane, a topical treatment for DFI.
Longboard has commenced the Phase III DEEp OCEAN Study of bexicaserin for treating seizures linked to DEEs in two years and ...
Zai Lab and argenx have announced receipt of approval from the National Medical Products Administration (NMPA) of China for ...