Theoretical and Natural Science
- The Open Access Proceedings Series for Conferences
Vol. 35, 26 April 2024
* Author to whom correspondence should be addressed.
Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by a gradual and irreversible decline in cognitive function. The underlying pathology involves the accumulation of amyloid beta, a protein implicated in the development and progression of the illness. Aducanumab is a type of human monoclonal antibody that exhibits preferential immunoreactivity towards both soluble and insoluble aggregates of Amyloid Beta (Aβ). Two phase 3 studies, namely EMERGE and ENGAGE, were conducted to evaluate the efficacy of aducanumab in individuals with early Alzheimer’s disease. These studies were designed identically, randomized, and double-blind in nature. Both trials were suspended early with the ineffective results shown in interim analysis for futility. Aducanumab was reassessed and met the primary and secondary clinical endpoints in EMERGE, but remains ineffective in ENGAGE. Reduction of Aβ plaques was observed in the high-dose group (10 mg/kg), showing a dose- and time-dependent pattern. The primary safety concern with Aducanumab is amyloid-related imaging abnormalities (ARIA), particularly in ApoEε4 carriers. Aducanumab is a new therapeutic strategy for AD, providing new treatment with disease-modifying potential. This paper evaluated the pharmacology, mechanism, clinical studies, and safety assessment of aducanumab. This research aims to provide a reference for the understanding of Aducanumab’s current research status and results.
Aducanumab, Alzheimer’s Disease, Amyloid beta, Clinical trials, Monoclonal antibody
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The datasets used and/or analyzed during the current study will be available from the authors upon reasonable request.
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