Results 91 to 100 of about 5,337 (191)
What should convince a clinician of disease modification in Alzheimer's disease clinical trials?
Abstract The recent publication of extension data from post‐regulatory trials of amyloid‐lowering antibody therapies, such as donanemab and lecanemab, requires clinicians to critically appraise trial designs and analyses in order to evaluate claims made by authors and sponsors of disease modification.
Jemma Hazan, Kathy Y. Liu, Robert Howard
wiley +1 more source
Abstract Cochrane Reviews are widely regarded as the gold standard for evidence synthesis, yet analytical framing influences interpretation. A recent Cochrane review of amyloid beta–targeting monoclonal antibodies pools mechanistically and biologically heterogenous interventions.
Betty M. Tijms +4 more
wiley +1 more source
Aggregation-dependent epitope sequence and modification fingerprints of anti-Aβ antibodies
A hallmark of Alzheimer’s disease (AD), the most common form of dementia, is the progressive accumulation of amyloid-beta (Aβ) peptides across distinct brain regions.
Ivan Talucci +14 more
doaj +1 more source
ABSTRACT Alzheimer's disease (AD) is a debilitating neurodegenerative condition characterized by progressive cognitive impairment, memory deterioration, and neuronal dysfunction. Its complex pathophysiology involves multiple interlinked processes, including amyloid‐β (Aβ) aggregation, tau hyperphosphorylation, oxidative stress, neuroinflammation ...
Amandeep Thakur +6 more
wiley +1 more source
Background Aducanumab is a human monoclonal antibody that selectively targets aggregated forms of amyloid beta (Aβ), including soluble oligomers and insoluble fibrils, and, at the writing of this , is currently under review by the US Food and Drug ...
Porter, Verna R. +15 more
core +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
Addendum: The antibody aducanumab reduces Aβ plaques in Alzheimer's disease.
This corrects the article DOI: 10.1038/nature21361. Erratum for An intermediate-mass black hole in the centre of the globular cluster 47 Tucanae. [Nature. 2017] The antibody aducanumab reduces Aβ plaques in Alzheimer's disease.
Grimm, Jan +6 more
core +1 more source
A real-world safety surveillance study of aducanumab through the FDA adverse event reporting system
BackgroundAlzheimer’s disease poses a major public health challenge, with aducanumab’s approval in 2021 as the first disease-modifying therapy raising important safety considerations.
Jingjing Huang +2 more
doaj +1 more source
Fit for purpose high‐throughput absolute quantitation of chimeric aducanumab in mouse cortex and plasma [PDF]
Background: Although pharmacokinetics and pharmacodynamics of biotherapeutics are commonly studied through ELISAs; however, the extremely strong binding of modern antibody‐based therapeutics result in background, inability of secondary antibody binding ...
Haynes, Kathryn A. +6 more
core +1 more source
Alzheimer's disease is a neurodegenerative disorder characterized by progressive cognitive decline and neuronal damage. Anti-amyloid monoclonal antibodies such as aducanumab, lecanemab, and donanemab, represent the first disease-modifying therapies for ...
Agnieszka Skoczeń +9 more
doaj +1 more source

