ArticlePloS one2020
Funders' data-sharing policies in therapeutic research: A survey of commercial and non-commercial funders.
Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
21 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Prevalence and predictors of data and code sharing in the medical and health sciences: systematic review with meta-analysis of individual participant data.BMJ (Clinical research ed.) · 2023Pooled it
- Incentivising research data sharing: a scoping review.Wellcome open research · 2021Pooled it
- Ethical Considerations for Clinical Data Sharing in Craniofacial Research: Recommendations From a Multidisciplinary Working Group.The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2026Article
- Data reuse in global health: perspectives from actors in policy, funding and research.BMJ global health · 2026Article
- A quantitative analysis of the use of anonymization in biomedical research.NPJ digital medicine · 2025Article
- Evaluating the discoverability of supporting research materials in ClinicalTrials.gov for US federally funded COVID-19 clinical studies.Journal of the Medical Library Association : JMLA · 2024Article
- Exploration of registration and the risk of bias in acupuncture randomised controlled trials: a systematic review protocol.BMJ open · 2024Article
- Article
- Responsibilities for receiving and using individual participant data.Cochrane evidence synthesis and methods · 2023Article
- Investigating the Secondary Use of Clinical Research Data: Protocol for a Mixed Methods Study.JMIR research protocols · 2023Article
- Ten (not so) simple rules for clinical trial data-sharing.PLoS computational biology · 2023Review
- Implementing clinical trial data sharing requires training a new generation of biomedical researchers.Nature medicine · 2023Article
- Ensuring Prevention Science Research is Synthesis-Ready for Immediate and Lasting Scientific Impact.Prevention science : the official journal of the Society for Prevention Research · 2022Article
- Advancing code sharing in the computational biology community.PLoS computational biology · 2022Article
- Data-sharing and re-analysis for main studies assessed by the European Medicines Agency-a cross-sectional study on European Public Assessment Reports.BMC medicine · 2022Article
- Article
- Promotion of data sharing needs more than an emergency: An analysis of trends across clinical trials registered on the International Clinical Trials Registry Platform.Wellcome open research · 2022Article
- Increasing best practice data sharing at PLOS Pathogens.PLoS pathogens · 2021Article
- Medical journal requirements for clinical trial data sharing: Ripe for improvement.PLoS medicine · 2021Article
- Status, use and impact of sharing individual participant data from clinical trials: a scoping review.BMJ open · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundFunders are key players in supporting randomized controlled trial (RCT) data-sharing. This research aimed to describe commercial and non-commercial funders' data-sharing policies and to assess the compliance of funded RCTs with the existing data-sharing policies. METHODS AND
findingsFunders of clinical research having funded at least one RCT in the years 2016 to 2018 were surveyed. All 78 eligible non-commercial funders retrieved from the Sherpa/Juliet Initiative website and a random sample of 100 commercial funders selected from pharmaceutical association member lists (LEEM, IFPMA, EFPIA) and the top 100 pharmaceutical companies in terms of drug sales were included. Thirty (out of 78; 38%) non-commercial funders had a data-sharing policy with eighteen (out of 30, 60%) making data-sharing mandatory and twelve (40%) encouraging data-sharing. Forty-one (out of 100; 41%) of commercial funders had a data-sharing policy. Among funders with a data-sharing policy, a survey of two random samples of 100 RCTs registered on Clinicaltrial.gov, data-sharing statements were present for seventy-seven (77%, 95% IC [67%-84%]) and eighty-one (81% [72% - 88%]) of RCTs funded by non-commercial and commercial funders respectively. Intention to share data was expressed in 12% [7%-20%] and 59% [49%- 69%] of RCTs funded by non-commercial and commercial funders respectively.
conclusionsThis survey identified suboptimal performances of funders in setting up data-sharing policies. For those with a data-sharing policy, the implementation of the policy in study registration was limited for commercial funders and of concern for non-commercial funders. The limitations of the present study include its cross-sectional nature, since data-sharing policies are continuously changing. We call for a standardization of policies with a strong evaluation component to make sure that, when in place, these policies are effective.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.