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Incidental findings in UK healthy volunteers screened for a COVID-19 vaccine trial.

Hodgson, SH; Iveson, P; Larwood, J; Roche, S; Morrison, H; Cosgrove, C; Galiza, E; Ikram, S; Lemm, N-M; Mehdipour, S; et al. Hodgson, SH; Iveson, P; Larwood, J; Roche, S; Morrison, H; Cosgrove, C; Galiza, E; Ikram, S; Lemm, N-M; Mehdipour, S; Owens, D; Pacurar, M; Schumacher, M; Shaw, RH; Faust, SN; Heath, PT; Pollard, AJ; Emary, KRW; Pollock, KM; Lazarus, R (2022) Incidental findings in UK healthy volunteers screened for a COVID-19 vaccine trial. Clin Transl Sci, 15 (2). pp. 524-534. ISSN 1752-8062 https://doi.org/10.1111/cts.13170
SGUL Authors: Heath, Paul Trafford Ikram, Sabina

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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.

Item Type: Article
Additional Information: © 2021 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
Keywords: 1102 Cardiorespiratory Medicine and Haematology, 1112 Oncology and Carcinogenesis, 1199 Other Medical and Health Sciences, General Clinical Medicine
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Clin Transl Sci
ISSN: 1752-8062
Language: eng
Dates:
DateEvent
13 February 2022Published
20 October 2021Published Online
13 September 2021Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Projects:
Project IDFunderFunder ID
MC_PC_19055Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
UNSPECIFIEDCoalition for Epidemic Preparedness Innovations (CEPI)UNSPECIFIED
UNSPECIFIEDNational Institute for Health ResearchUNSPECIFIED
UNSPECIFIEDNIHR Oxford Biomedical Research CentreUNSPECIFIED
UNSPECIFIEDNIHR Southampton Clinical Research Facility and NIHR Southampton Biomedical Research CentreUNSPECIFIED
UNSPECIFIEDUniversity Hospital Southampton NHS Foundation TrustUNSPECIFIED
UNSPECIFIEDNIHR Imperial Clinical Research FacilityUNSPECIFIED
UNSPECIFIEDNIHR North West London, South London, Wessex, and West of England Local Clinical Research NetworksUNSPECIFIED
UNSPECIFIEDNIHR Oxford Health Biomedical Research CentreUNSPECIFIED
PubMed ID: 34670021
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113796
Publisher's version: https://doi.org/10.1111/cts.13170

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