The approval of Aβ-clearing antibodies like Leqembi (lecanemab) and Kisunla (donanemab) marked a landmark shift toward disease-modifying therapies in Alzheimer’s,…
BUSINESS
PDUFA Date Set for Jan. 31, 2017 for Daiichi Sankyo’s Nausea Drug
Daiichi Sankyo said that the US FDA has accepted its new drug application for the nausea drug CL-108 it licensed from US pain specialty firm Charleston Laboratories, with a target action date under the Prescription Drug User Fee Act (PDUFA)…
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