Eli Lilly Donanemab secures CDSCO nod for early symptomatic Alzheimer's Disease
Written By : Ruchika Sharma
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2025-11-18 10:00 GMT | Update On 2025-11-18 10:00 GMT
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New Delhi: Eli Lilly and Company (India) has secured marketing authorization for donanemab (350 mg/20 mL administered every four weeks via intravenous infusion as described in the prescribing information) from the Central Drugs Standard Control Organization (CDSCO) for the treatment of Alzheimer’s disease (AD) in adults with early symptomatic stages. This includes individuals with mild cognitive impairment (MCI) and those in the mild dementia stage of AD, with confirmed amyloid pathology.
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