Results 31 to 40 of about 2,875 (114)
ABSTRACT Early cognitive decline may become evident through changes in daily activities or behaviour before it is apparent in a brief consultation. This selective narrative review supports case‐finding and appropriate referral in general and psychiatric practice.
Kengo Shimoda
wiley +1 more source
Introduction Donanemab, a monoclonal antibody directed against an insoluble, modified, N-terminal truncated form of amyloid beta, demonstrated efficacy and safety in patients with early, symptomatic Alzheimer’s disease (AD) in the phase 3 TRAILBLAZER-ALZ
Shoichiro Sato +5 more
doaj +1 more source
INTRODUCTION Infusion‐related reactions (IRRs) and hypersensitivity are adverse events associated with therapeutic antibodies. Characterization of IRRs can lead to improved risk anticipation and management of this event.
Paul Ardayfio +16 more
doaj +1 more source
Abstract Since the groundbreaking work of Alois Alzheimer in the early 1900s, Alzheimer's disease research has evolved immensely, most notably with the establishment of the Alzheimer's Disease Research Centers (ADRC). Fueled by the vision and funding of the National Institute on Aging (NIA), ADRCs have created a legacy through their work standardizing ...
John H. Growdon +4 more
wiley +1 more source
Optimal anti-amyloid-beta therapy for Alzheimer's disease via a personalized mathematical model.
With the recent approval by the FDA of the first disease-modifying drug for Alzheimer's Disease (AD), personalized medicine will be increasingly important for appropriate management and counseling of patients with AD and those at risk.
Wenrui Hao +2 more
doaj +1 more source
Longitudinal clinical outcomes after amyloid clearance in aducanumab phase 3 studies
Abstract INTRODUCTION Anti‐amyloid antibody clinical trials with a high proportion of participants reaching treatment‐related amyloid clearance (TRAC) had positive clinical outcomes. We evaluated the aducanumab phase 3 program to determine whether TRAC during the double‐blind period was likewise associated with clinical benefit.
Menglan Pang +8 more
wiley +1 more source
Safety Concerns in Neurological Clinical Trials: A Challenge That the FDA Must Resolve
Background: Monoclonal antibodies approved by the FDA, lecanemab, donanemab, and aducanumab, are failing to meet the expected efficacy to treat early Alzheimer’s disease, and aducanumab has been recalled.
Sarfaraz K. Niazi
doaj +1 more source
Abstract INTRODUCTION Whether glucagon‐like peptide‐1 (GLP‐1) receptor (GLP‐1R) activation lowers Alzheimer's disease (AD) risk via peripheral metabolic improvement or direct neuroprotection remains unclear. METHODS Using blood and brain‐cortex cis‐acting expression quantitative trait loci (cis‐eQTLs) for GLP‐1R as instruments, we performed cis ...
Li Jiang +17 more
wiley +1 more source
INTRODUCTION This study investigated evidence for or against a difference in treatment effect between women and men for lecanemab and donanemab. METHODS Data were derived from supplementary analyses of the regulatory studies CLARITY‐AD (lecanemab) and ...
Stefan J. Teipel +2 more
doaj +1 more source
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.
Wenjing Wu +14 more
wiley +1 more source

