Project Lightspeed: A Case Study in Research Ethics and Accelerated Vaccine Development

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Bibliographic Details
Title: Project Lightspeed: A Case Study in Research Ethics and Accelerated Vaccine Development
Language: English
Authors: Klaus Leisinger, Doris Schroeder (ORCID 0000-0002-3633-2758)
Source: Research Ethics. 2024 20(4):847-856.
Availability: SAGE Publications. 2455 Teller Road, Thousand Oaks, CA 91320. Tel: 800-818-7243; Tel: 805-499-9774; Fax: 800-583-2665; e-mail: journals@sagepub.com; Web site: https://sagepub.com
Peer Reviewed: Y
Page Count: 10
Publication Date: 2024
Document Type: Journal Articles
Reports - Research
Descriptors: Scientific Research, Research Methodology, Immunization Programs, COVID-19, Pandemics, Ethics, Experimental Programs, Decision Making, Trust (Psychology), Efficiency, Governance, Compliance (Legal)
DOI: 10.1177/17470161241251597
ISSN: 1747-0161
2047-6094
Abstract: The COVID-19 pathogen led to a fast expanding pandemic because it proved lethal in certain populations but could be transmitted by persons who appeared healthy. As a result, researchers came under unprecedented time pressure to develop a vaccine. This case study focuses on the first COVID-19 vaccine, which was approved for use in humans, known as Comirnaty, the BioNTech-Pfizer COVID-19 vaccine or Vaccine BNT162b2. With the benefit of hindsight, we show how close collaboration with regulators and trust-based decisions meant that the race for a COVID-19 vaccine was won without purposefully infecting healthy participants with an infectious agent that can cause severe illness or death and for which no rescue therapy had existed.
Abstractor: As Provided
Entry Date: 2024
Accession Number: EJ1443228
Database: ERIC
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Description
Abstract:The COVID-19 pathogen led to a fast expanding pandemic because it proved lethal in certain populations but could be transmitted by persons who appeared healthy. As a result, researchers came under unprecedented time pressure to develop a vaccine. This case study focuses on the first COVID-19 vaccine, which was approved for use in humans, known as Comirnaty, the BioNTech-Pfizer COVID-19 vaccine or Vaccine BNT162b2. With the benefit of hindsight, we show how close collaboration with regulators and trust-based decisions meant that the race for a COVID-19 vaccine was won without purposefully infecting healthy participants with an infectious agent that can cause severe illness or death and for which no rescue therapy had existed.
ISSN:1747-0161
2047-6094
DOI:10.1177/17470161241251597