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frrol

04/27/24 8:26 AM

#457775 RE: Hosai #457772

The past few years the EMA have had huge demand on their AD rapporteur roster. They're currently assessing lecanemab and donanemab, and they've been dragging on. Wouldn't be surprised if that was a factor in delay. Lecan is having procedural issues, and donan was being assessed for accelerated assessment last year (can't find out current status).

Steady_T

04/27/24 2:26 PM

#457791 RE: Hosai #457772

Thanks for the clarification.