July 2026 Eisai Co., Ltd. and Biogen Inc. received U.S. FDA approval for the subcutaneous starter-dose formulation of Leqembi® (lecanemab-irmb), enabling at-home initiation with caregiver assistance and improving access to Alzheimer's disease treatment in North America.
April 2026 Axsome Therapeutics received U.S. FDA approval for Auvelity® as the first non-antipsychotic treatment indicated for agitation associated with dementia due to Alzheimer's disease, expanding therapeutic options for neurodegenerative disease management in North America.
October 2025 Alpha Cognition Inc. commercially expanded the availability of ZUNVEYL® (benzgalantamine) across the United States through specialty pharmacy and long-term care distribution channels, strengthening treatment options for patients with mild-to-moderate Alzheimer's disease.
July 2025 Eli Lilly and Company received U.S. FDA approval for an updated prescribing framework for Kisunla® (donanemab-azbt), supporting its commercialization for adults with early symptomatic Alzheimer's disease in the United States and expanding access to disease-modifying therapy.