ARIA in Patients Treated With Lecanemab (BAN2401) in a Phase 2 Study in Early Alzheimer's Disease
INTRODUCTION Lecanemab is a humanized immunoglobulin G1 (IgG1) monoclonal antibody that preferentially targets soluble aggregated Aβ species (protofibrils) with activity at amyloid plaques.
Lawrence S Honig +2 more
exaly +2 more sources
Caregiver positivity as a psychosocial modifier of lecanemab-related outcomes in Alzheimer's disease: A multicenter longitudinal study in China. [PDF]
Abstract INTRODUCTION Real‐world modifiers of lecanemab benefit in Alzheimer's disease (AD) remain elusive. We examined associations between caregiver positivity and longitudinal outcomes in AD. METHODS This seven‐center longitudinal study followed 127 biomarker‐supported AD patient–caregiver dyads over 18 months.
Wu W +14 more
europepmc +2 more sources
Use of Lecanemab for the Treatment of Alzheimer's Disease: A Systematic Review
Purpose The US Food and Drug Administration authorized lecanemab for the therapeutic use of Alzheimer's disease (AD) in January 2023. To assess the effectiveness and safety of lecanemab in treating AD, we thoroughly examined the studies that are ...
Md Fahad Hossain
exaly +2 more sources
ObjectiveWe performed a systematic review and meta-analysis of the cognitive effectiveness and safety of lecanemab on subjects with Alzheimer's disease (AD).MethodsWe screened the literature published before February 2023 in PubMed, Embase, Web of ...
Yuewei Chi, Yue Qiao
exaly +3 more sources
Real‐world evidence for amyloid‐targeted therapies: Lecanemab and donanemab [PDF]
INTRODUCTION Real‐world safety data on amyloid‐targeted therapies in early Alzheimer's disease remain limited, particularly for modified donanemab titration and direct lecanemab–donanemab comparisons.
Ryan Hakim +8 more
doaj +2 more sources
Real-world effectiveness of monoclonal antibody lecanemab versus acetylcholinesterase inhibitors in Alzheimer’s disease: a target trial emulation [PDF]
Background Acetylcholinesterase inhibitors (AChEIs) provide symptomatic relief in Alzheimer’s disease (AD), whereas lecanemab may modify disease progression; however, real-world evidence on its safety and clinical impact remains limited.
Chuo-Yu Lee +11 more
doaj +2 more sources
Dementia with Lewy bodies and amyloid pathology: Eligible for anti‐amyloid treatment or not? [PDF]
Abstract In the future, treatment of dementia will be personalized, targeted to contributing pathologies, rather than the clinical syndrome. Anti‐amyloid drugs for Alzheimer's disease are the first approved drugs; however, the impact of co‑pathology on the treatment effects remains incomplete.
Exalto L +6 more
europepmc +2 more sources
Real‐world implementation of lecanemab in Alzheimer's disease: A Japanese cohort [PDF]
INTRODUCTION Real‐world evidence for lecanemab remains limited, particularly among Asian populations. We evaluated the feasibility, safety, biomarker profiles, and short‐term clinical outcomes of lecanemab in practice in Japan.
Sho Shimohama +13 more
doaj +2 more sources
Post-marketing safety of lecanemab: a real-world study based on FAERS database, multicenter cohort and network pharmacology [PDF]
IntroductionLecanemab is a monoclonal antibody targeting amyloid-beta (Aβ) approved for treating Alzheimer’s disease (AD) with mild cognitive impairment or mild dementia. Continuous monitoring of its real-world safety profile remains essential.
Xiaoxuan Xing +13 more
doaj +2 more sources
Post-marketing safety signals and report-level ARIA-E stratification for lecanemab and donanemab: an integrated FAERS and WHO-VigiAccess pharmacovigilance study [PDF]
Background: Anti-β-amyloid monoclonal antibodies provide a disease-modifying treatment approach for Alzheimer’s disease, but post-marketing safety concerns remain, particularly amyloid-related imaging abnormalities (ARIA).
Wei-Yang Xue +6 more
doaj +2 more sources

