Compliance with results reporting at ClinicalTrials.gov.

dc.contributor.author

Anderson, Monique L

dc.contributor.author

Chiswell, Karen

dc.contributor.author

Peterson, Eric D

dc.contributor.author

Tasneem, Asba

dc.contributor.author

Topping, James

dc.contributor.author

Califf, Robert M

dc.coverage.spatial

United States

dc.date.accessioned

2016-11-30T19:52:30Z

dc.date.issued

2015-03-12

dc.description.abstract

BACKGROUND: The Food and Drug Administration Amendments Act (FDAAA) mandates timely reporting of results of applicable clinical trials to ClinicalTrials.gov. We characterized the proportion of applicable clinical trials with publicly available results and determined independent factors associated with the reporting of results. METHODS: Using an algorithm based on input from the National Library of Medicine, we identified trials that were likely to be subject to FDAAA provisions (highly likely applicable clinical trials, or HLACTs) from 2008 through 2013. We determined the proportion of HLACTs that reported results within the 12-month interval mandated by the FDAAA or at any time during the 5-year study period. We used regression models to examine characteristics associated with reporting at 12 months and throughout the 5-year study period. RESULTS: From all the trials at ClinicalTrials.gov, we identified 13,327 HLACTs that were terminated or completed from January 1, 2008, through August 31, 2012. Of these trials, 77.4% were classified as drug trials. A total of 36.9% of the trials were phase 2 studies, and 23.4% were phase 3 studies; 65.6% were funded by industry. Only 13.4% of trials reported summary results within 12 months after trial completion, whereas 38.3% reported results at any time up to September 27, 2013. Timely reporting was independently associated with factors such as FDA oversight, a later trial phase, and industry funding. A sample review suggested that 45% of industry-funded trials were not required to report results, as compared with 6% of trials funded by the National Institutes of Health (NIH) and 9% of trials that were funded by other government or academic institutions. CONCLUSIONS: Despite ethical and legal obligations to disclose findings promptly, most HLACTs did not report results to ClinicalTrials.gov in a timely fashion during the study period. Industry-funded trials adhered to legal obligations more often than did trials funded by the NIH or other government or academic institutions. (Funded by the Clinical Trials Transformation Initiative and the NIH.).

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/25760355

dc.identifier.eissn

1533-4406

dc.identifier.uri

https://hdl.handle.net/10161/13024

dc.language

eng

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Massachusetts Medical Society

dc.relation.ispartof

N Engl J Med

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10.1056/NEJMsa1409364

dc.subject

Algorithms

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Clinical Trials as Topic

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Databases, Factual

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Disclosure

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Drug Industry

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Government Regulation

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Humans

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Mandatory Programs

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National Library of Medicine (U.S.)

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Proportional Hazards Models

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Registries

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Research Support as Topic

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United States

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United States Food and Drug Administration

dc.title

Compliance with results reporting at ClinicalTrials.gov.

dc.type

Journal article

duke.contributor.orcid

Anderson, Monique L|0000-0003-4719-399X

duke.contributor.orcid

Chiswell, Karen|0000-0002-0279-9093

duke.contributor.orcid

Peterson, Eric D|0000-0002-5415-4721

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/25760355

pubs.begin-page

1031

pubs.end-page

1039

pubs.issue

11

pubs.organisational-group

Clinical Science Departments

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Duke

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Duke Clinical Research Institute

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Institutes and Centers

pubs.organisational-group

Medicine

pubs.organisational-group

Medicine, Cardiology

pubs.organisational-group

School of Medicine

pubs.organisational-group

Staff

pubs.publication-status

Published

pubs.volume

372

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