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Eli Lilly requests re-examination of Alzheimer's drug recommendation

Eli Lilly has requested that the EMA re-examine its opinion on the company's Alzheimer's drug, Kisunla, the agency announced on Friday.

Kisunla (donanemab) has already been granted market approval in the United States, but in late March, the Europe's medicines regulator (EMA) issued a different assessment.

Kisunla has been developed to slow the progression of Alzheimer's disease in adult patients with amyloid-beta plaques in the brain and mild cognitive impairment or mild dementia due to Alzheimer's disease.

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