US Food and Drug Administration Approval of Aducanumab-Is Amyloid Load a Valid Surrogate End Point for Alzheimer Disease Clinical Trials?

JAMA Neurol. 2021 Nov 1;78(11):1307-1308. doi: 10.1001/jamaneurol.2021.3126.
No abstract available

MeSH terms

  • Alzheimer Disease / drug therapy*
  • Amyloid beta-Peptides / drug effects*
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Biomarkers*
  • Clinical Trials as Topic / standards*
  • Drug Approval*
  • Humans
  • United States
  • United States Food and Drug Administration

Substances

  • Amyloid beta-Peptides
  • Antibodies, Monoclonal, Humanized
  • Biomarkers
  • aducanumab