Biogen was today due to appear before the European Medicines Agency at an oral explanation meeting relating to the regulator’s re-examination of its recommendation last year that the company’s Alzheimer’s disease drug, Aduhelm (aducanumab), should not be approved for use in the EU.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?