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
- Lilly Confirms Orforglipron Diabetes Filings in US, Japan
August 7, 2026
- Takeda Snares US Approval for Orzeyful in Narcolepsy Type 1
August 7, 2026
- Inrebic Expands First-Line Treatment Options for Myelofibrosis: Expert
August 7, 2026
- Meiji Pharma Drops Hiyasta Development in B-Cell NHL
August 7, 2026
- AstraZeneca Japan Chief Says MFN Response Requires Drug Pricing Reform
August 5, 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.…





