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…
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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…





