Incidental findings in UK healthy volunteers screened for a COVID-19 vaccine trial
- PMID: 34670021
- PMCID: PMC8652599
- DOI: 10.1111/cts.13170
Incidental findings in UK healthy volunteers screened for a COVID-19 vaccine trial
Abstract
The safety of novel therapeutics and vaccines are typically assessed in early phase clinical trials involving "healthy volunteers." Abnormalities in such individuals can be difficult to interpret and may indicate previously unrecognized medical conditions. The frequency of incidental findings (IFs) in healthy volunteers who attend for clinical trial screening is unclear. To assess this, we retrospectively analyzed data for 1838 "healthy volunteers" screened for enrolment in a UK multicenter, phase I/II severe acute respiratory syndrome-coronavirus 2 (SARS-COV-2) vaccine trial. Participants were predominantly White (89.7%, 1640/1828) with a median age of 34 years (interquartile range [IQR] = 27-44). There were 27.7% of participants (510/1838) who had at least one IF detected. The likelihood of identifying evidence of a potential, new blood-borne virus infection was low (1 in 238 participants) compared with identification of an elevated alanine transaminase (ALT; 1 in 17 participants). A large proportion of participants described social habits that could impact negatively on their health; 21% consumed alcohol in excess, 10% were current smokers, 11% described recreational drug use, and only 48% had body weight in the ideal range. Our data demonstrate that screening prior to enrollment in early phase clinical trials identifies a range of IFs, which should inform discussion during the consent process. Greater clarity is needed to ensure an appropriate balance is struck between early identification of medical problems and avoidance of exclusion of volunteers due to spurious or physiological abnormalities. Debate should inform the role of the trial physician in highlighting and advising about unhealthy social habits.
© 2021 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.
Conflict of interest statement
All authors have worked or are currently working on the UK clinical trials of the SARS‐COV‐2 candidate vaccine; ChAdOx‐1 nCoV‐19. AJP is Chair of UK Dept. Health and Social Care's (DHSC) Joint Committee on Vaccination & Immunisation (JCVI), and is a member of the WHO’s SAGE. The views expressed in this article do not necessarily represent the views of DHSC, JCVI, NIHR or WHO. AJP is the Chief Investigator of UK studies of ChAdOx nCoV‐2 vaccine. The University of Oxford has entered into a partnership with AstraZeneca on coronavirus vaccine development. SNF acts as UK Chief Investigator for other commercial and non‐commercial COVID‐19 vaccines studies (Janssen adult and paediatric COVID‐19 vaccine trials, Valneva COVID‐19 vaccine trials, Oxford/AZ paediatric vaccine trial and the Imperial College COVID‐19 vaccine trial). PTH acts as UK Chief Investigator for the Novavax COVID 19 vaccine trial and as an investigator for other commercial and non‐commercial COVID‐19 vaccine trials (Valneva COVID‐19 vaccine trials, Oxford/AZ paediatric vaccine trial, Pfizer pregnancy COVID‐19 trial and the Imperial College COVID‐19 vaccine trial). KMP acts as Chief Investigator and investigator for other commercial and non‐commercial COVID‐19 vaccine studies (Imperial College London COVID‐19 vaccine trial and Janssen adult COVID‐19 vaccine trial). RL acts as Principal and Chief Investigator for other commercial and non‐commercial COVID 19 vaccine studies (Valneva COVID‐19 vaccine trials, University of Oxford COMCOV study, Janssen adult COVID‐19 vaccine trial).
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