July 2026 Eisai and Biogen received U.S. FDA approval for LEQEMBI IQLIK® (lecanemab-irmb), a once-weekly subcutaneous autoinjector formulation for early Alzheimer's disease, expanding treatment access through at-home administration.
May 2026 Health Canada approved Kisunla™ (donanemab) from Eli Lilly for adults with early symptomatic Alzheimer's disease, expanding the availability of disease-modifying dementia therapies in Canada.
April 2026 The U.S. FDA approved an expanded indication for Auvelity® (dextromethorphan/bupropion) as the first non-antipsychotic treatment for agitation associated with dementia due to Alzheimer's disease.
January 2026 Alpha Cognition commercially launched ZUNVEYL® (benzgalantamine) in the United States, expanding treatment options for mild-to-moderate Alzheimer's disease with a prodrug formulation designed to improve gastrointestinal tolerability.
June 2025 Eli Lilly expanded the global rollout of Kisunla® (donanemab) through additional regulatory submissions and commercialization initiatives following approvals in major markets, strengthening its Alzheimer's disease treatment portfolio.