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Clinical trials of new drugs for Alzheimer disease: a 2020-2023 update. | LitMetric

Clinical trials of new drugs for Alzheimer disease: a 2020-2023 update.

J Biomed Sci

PhD Program in Medical Neuroscience, College of Medical Science and Technology, Taipei Medical University, No. 291, Zhong Zheng Road, Zhonghe District, New Taipei City, Taiwan.

Published: October 2023

AI Article Synopsis

  • Alzheimer's disease (AD) is the leading cause of dementia and involves various harmful processes in the brain, such as amyloid and tau accumulation, inflammation, and neuron damage.
  • The US-FDA has recently approved two new drugs, Aducanumab and Lecanemab, targeting amyloid, marking a significant advancement after nearly 20 years without new treatments.
  • Current clinical trials are focusing on developing disease-modifying therapies that target the underlying causes of AD and are increasingly recruiting participants at earlier disease stages, emphasizing the importance of research in prevention and intervention.

Article Abstract

Alzheimer's disease (AD) is the leading cause of dementia, presenting a significant unmet medical need worldwide. The pathogenesis of AD involves various pathophysiological events, including the accumulation of amyloid and tau, neuro-inflammation, and neuronal injury. Clinical trials focusing on new drugs for AD were documented in 2020, but subsequent developments have emerged since then. Notably, the US-FDA has approved Aducanumab and Lecanemab, both antibodies targeting amyloid, marking the end of a nearly two-decade period without new AD drugs. In this comprehensive report, we review all trials listed in clinicaltrials.gov, elucidating their underlying mechanisms and study designs. Ongoing clinical trials are investigating numerous promising new drugs for AD. The main trends in these trials involve pathophysiology-based, disease-modifying therapies and the recruitment of participants in earlier stages of the disease. These trends underscore the significance of conducting fundamental research on pathophysiology, prevention, and intervention prior to the occurrence of brain damage caused by AD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544555PMC
http://dx.doi.org/10.1186/s12929-023-00976-6DOI Listing

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