Eisai said on July 2 that UK regulatory authorities have accepted for review a marketing authorization application for its in-house-developed orexin receptor antagonist Dayvigo (lemborexant) for the treatment of adult insomnia. The application, filed with the Medicines and Healthcare products…
To read the full story
Related Article
- Eisai’s Dayvigo Accepted for EMA Review
July 17, 2026
BUSINESS
- Shionogi Pivoting to Function-Based Model in Global HR Revamp
September 1, 2026
- SanBio to Move All Akuugo Manufacturing to Minaris’ Yokohama Site
September 1, 2026
- Merck KGaA to Consolidate Japan Life Science Labs at Haneda Hub
September 1, 2026
- FDA Approves Takeda’s PV Drug Mimrylo
September 1, 2026
- Sarclisa SC Can Meet Patient, Healthcare Worker Needs: Specialist
September 1, 2026
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





