EMA säger nej till Eli Lillys alzheimerläkemedel

Den europeiska läkemedelsmyndigheten EMA rekommenderar att Eli Lillys alzheimerkandidat Kisunla nekas godkännande i EU. Nyttan med behandlingen bedöms inte överväga riskerna för potentiellt dödliga biverkningar i form av hjärnsvullnad.

By Anders Göransson

March 31, 2025 10:26 AM

Kisunla (donanemab) har utvecklats för att bromsa utvecklingen av Alzheimers sjukdom hos vuxna patienter med amyloid-beta-plack i hjärnan och en mild kognitiv nedsättning eller mild demens på grund av Alzheimers sjukdom.

I bland annat USA har läkemedlet beviljats marknadsgodkännande, men EMA gör en annan bedömning.

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