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. 2021 Jan 15;22(1):59.
doi: 10.1186/s13063-021-05024-y.

Missing clinical trial data: the evidence gap in primary data for potential COVID-19 drugs

Affiliations

Missing clinical trial data: the evidence gap in primary data for potential COVID-19 drugs

Florence Rodgers et al. Trials. .

Abstract

Background: Several drugs are being repurposed for the treatment of the coronavirus disease 2019 (COVID-19) pandemic based on in vitro or early clinical findings. As these drugs are being used in varied regimens and dosages, it is important to enable synthesis of existing safety data from clinical trials. However, availability of safety information is limited by a lack of timely reporting of overall clinical trial results on public registries or through academic publication. We aimed to analyse the evidence gap in this data by conducting a rapid review of results posting on ClinicalTrials.gov and in academic publications to quantify the number of trials missing results for drugs potentially being repurposed for COVID-19.

Methods: ClinicalTrials.gov was searched for 19 drugs that have been identified as potential treatments for COVID-19. Relevant clinical trials for any prior indication were listed by identifier (NCT number) and checked for results and for timely result reporting (within 395 days of the primary completion date). Additionally, PubMed and Google Scholar were searched to identify publications of results not listed on the registry. A second, blinded search of 10% of trials was conducted to assess reviewer concordance.

Results: Of 3754 completed trials, 1516 (40.4%) did not post results on ClinicalTrials.gov or in the academic literature. Tabular results were available on ClinicalTrials.gov for 1172 (31.2%) completed trials. A further 1066 (28.4%) had published results in the academic literature, but did not report results on ClinicalTrials.gov . Key drugs missing clinical trial results include hydroxychloroquine (37.0% completed trials unreported), favipiravir (77.8%) and lopinavir (40.5%).

Conclusions: There is an important evidence gap for the safety of drugs being repurposed for COVID-19. This uncertainty could cause unnecessary additional morbidity and mortality during the pandemic. We recommend caution in experimental drug use for non-severe disease and urge clinical trial sponsors to report missing results retrospectively.

Keywords: Adverse events; COVID-19 treatment; Clinical trial transparency; Coronavirus; Repurposed drugs; Safety information.

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Conflict of interest statement

Three of the co-authors on this paper are part of Universities Allied for Essential Medicines U.K. However, views expressed in this paper are not necessarily that of Universities Allied for Essential Medicines Europe.

Figures

Fig. 1
Fig. 1
Flow chart depicting the methodology used to search for and identify relevant publications for each of the trials listed on CT.gov
Fig. 2
Fig. 2
Flow diagram displaying the numbers of registered trials identified on CT.gov and the proportion of these which ultimately have no results available. The number of trials which had results available from various sources or had been withdrawn/suspended or trails for which results were not yet due are also shown
Fig. 3
Fig. 3
Bar chart displaying the proportion of trial results available across all potential COVID-19 therapies—categorised into those registered fully on CT.gov, those with results available in the academic literature only and those with no results available

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