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
- Terumo to Take US$610 Million Hit as CSL Plasma Supply Deal Ends
October 9, 2026
- TOPIX Shuffle Puts Mid-Tier Drug Makers, Wholesalers on Chopping Block
October 9, 2026
- Ono Gets Japan, Asia Rights to 3 IgG Degraders from Biohaven
October 9, 2026
- Datroway Snares TNBC Approval in China: Daiichi Sankyo
October 9, 2026
- Enhertu Gains Adjuvant Nod in China for HER2-Positive Breast Cancer
October 9, 2026
The Wednesday TableShe had been on virtual calls since eight in the morning. The screen glowed. Her eyes burned. Plugged into Teams across time zones, she was digitally connected yet entirely isolated from the reality of Japan’s pharma market.She needed…





