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Considerations for unblinding individual study participants during vaccine trials

  • members of the SPEAC meta-DSMB
  • Johns Hopkins University
  • London School of Hygiene & Tropical Medicine
  • Coalition for Epidemic Preparedness Innovations
  • Vanderbilt University
  • Stanford University School of Medicine
  • Directorate General for Disease Surveillance and Control
  • Executive Director of The INCLEN Trust International
  • University of Melbourne
  • Finnish Institute for Health and Welfare (THL)
  • University of Basel
  • Institut Pasteur Korea
  • University of Jordan
  • University of Nebraska Medical Center
  • Emory University
  • Mahidol University
  • São Paulo School of Medical Sciences
  • Global Vaccine Data Network

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Premature unblinding of individual participants is rarely reported in publications, but such unblinding can disrupt vaccine trials by causing worry and drop-out of other participants or “pseudo unblinding,” in which participants or investigators over-interpret certain symptoms as being related to receiving an investigational product. This review summarizes appropriate reasons for unblinding in vaccine trials. Regulatory guidance could be improved by distinguishing guidance for vaccine trials from drug trials, with the recognition that unblinding individual participants in vaccine studies is rarely needed for management of adverse events following immunization.

Original languageEnglish
Pages (from-to)3399-3402
Number of pages4
JournalVaccine
Volume41
Issue number22
DOIs
Publication statusPublished - 22 May 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adverse events
  • Regulatory guidance
  • Unblinding
  • Vaccine
  • Vaccine safety
  • Vaccine trials

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