BioArctic Partner Eisai Reports the MAA Submission to the MHRA for Lecanemab to Treat Early Alzheimer's Disease
- The company has submitted an MAA to the MHRA for lecanemab, an investigational anti-amyloid beta (Aβ) protofibril Ab to treat early AD. The MAA was based on the results from the confirmatory P-III study (Clarity AD) & the P-IIb study evaluating lecanemab
- The results showed that patients treated with lecanemab achieved a reduction of clinical decline over PBO after 18mos. The (Clarity AD) study met its 1EPs & 2EPs with highly significant results
- Lecanemab may have the ability to impact disease pathology & slow down the progression of the disease. BioArctic gets the rights to commercialize lecanemab in the Nordic region while Eisai & BioArctic are preparing for joint commercialization in the region
Ref: PRNewswire | Image: BioArctic
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