Eisai said on July 16 that the European Medicines Agency (EMA) has accepted for review a marketing authorization application for its orexin receptor antagonist Dayvigo (lemborexant) for the treatment of chronic insomnia in adults.Dayvigo was approved in the US in…
To read the full story
Related Article
- Eisai’s Dayvigo Accepted for UK Regulatory Review
July 3, 2026
BUSINESS
- Japan Pharma Market Seen Topping 11 Trillion Yen by 2035: Fuji Keizai
August 26, 2026
- Belite Bio Eyes Japan Filing for Stargardt Drug within 3 Months
August 26, 2026
- Sandoz to Sell, Distribute G-Lasta Biosimilar in Japan
August 26, 2026
- Astellas Starts Global PIII of ASP2138 in Gastric Cancer
August 26, 2026
- Chugai Files Vamikibart in Japan for Uveitic Macular Edema
August 26, 2026
A few weeks ago, I had coffee with a very talented executive. Let’s call him Kenji. He has a great job, a big salary, and a solid team. But he was unhappy. He felt bored and wanted a new challenge.…





