EMA planerar möte om lecanemab

Den europeiska läkemedelsmyndigheten EMA:s vetenskapliga rådgivande grupp (SAG) väntas inom kort sammanträda för att diskutera ansökan om marknadsgodkännande för Alzheimerläkemedlet lecanemab.

By Anders Göransson

January 11, 2024 9:58 AM

"Ansökan granskas för närvarande av EMA. Mötet för SAG förväntas äga rum under första kvartalet 2024", skriver Bioarctic i ett pressmeddelande, där man hänvisar till uppgifter från sin partner Eisai.

Eisai räknar med att Europeiska kommissionens beslut om marknadsgodkännande av lecanemab kommer under andra kvartalet 2024. om ett yttrande från CHMP, EMA:s expertkommitté för humanmedicin, kommit senast den 31 mars,

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