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Data and Safety Monitoring of COVID-19 Vaccine Clinical Trials.
Joffe, Steven; Babiker, Abdel; Ellenberg, Susan S; Fix, Alan; Griffin, Marie R; Hunsberger, Sally; Kalil, Jorge; Levine, Myron M; Makgoba, Malegapuru W; Moore, Reneé H; Tsiatis, Anastasios A; Whitley, Richard.
  • Joffe S; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Babiker A; Medical Research Council Clinical Trials Unit, University College London, London, United Kingdom.
  • Ellenberg SS; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Fix A; Center for Vaccine Innovation and Access, PATH, Washington, District of Columbia, USA.
  • Griffin MR; Vanderbilt School of Medicine, Nashville, Tennessee, USA.
  • Hunsberger S; National Institute of Allergy and Infectious Disease, Rockville, Maryland, USA.
  • Kalil J; Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
  • Levine MM; University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Makgoba MW; Health Ombudsman, Office of Health Standards and Compliance, Pretoria, Republic of South Africa.
  • Moore RH; Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
  • Tsiatis AA; North Carolina State University, Raleigh, North Carolina, USA.
  • Whitley R; University of Alabama at Birmingham, Birmingham, Alabama, USA.
J Infect Dis ; 224(12): 1995-2000, 2021 12 15.
Article in English | MEDLINE | ID: covidwho-1233857
ABSTRACT
To speed the development of vaccines against SARS-CoV-2, the United States Federal Government has funded multiple phase 3 trials of candidate vaccines. A single 11-member data and safety monitoring board (DSMB) monitors all government-funded trials to ensure coordinated oversight, promote harmonized designs, and allow shared insights related to safety across trials. DSMB reviews encompass 3 domains (1) the conduct of trials, including overall and subgroup accrual and data quality and completeness; (2) safety, including individual events of concern and comparisons by randomized group; and (3) interim analyses of efficacy when event-driven milestones are met. Challenges have included the scale and pace of the trials, the frequency of safety events related to the combined enrollment of over 100 000 participants, many of whom are older adults or have comorbid conditions that place them at independent risk of serious health events, and the politicized environment in which the trials have taken place.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Aged / Humans Country/Region as subject: North America Language: English Journal: J Infect Dis Year: 2021 Document Type: Article Affiliation country: Infdis

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Aged / Humans Country/Region as subject: North America Language: English Journal: J Infect Dis Year: 2021 Document Type: Article Affiliation country: Infdis