News

WHO Launches Initiative to Standardize Clinical Trial Data


 

The World Health Organization has launched a major initiative to standardize the way that information on clinical trials is made available to the public.

In an attempt to address growing public concerns about the transparency of medical research involving human participants, WHO is recommending 20 key details that all clinical trial registries should include.

“Registration of all clinical trials and full disclosure of key information at the time of registration are fundamental to ensuring transparency in medical research and fulfilling ethical responsibilities to patients and study participants,” Dr. Timothy Evans, assistant director-general of the WHO, said in a written statement.

WHO's International Clinical Trials Registry Platform is not itself a registry but provides standards for all clinical trial registries. These standards require information about sources of monetary or material support, primary and secondary sponsors, contacts for public and scientific queries, countries of recruitment, health conditions or problems studied, interventions, key inclusion and exclusion criteria, study design, date of first enrollment, target sample size, recruitment status, and primary and secondary outcomes.

The voluntary initiative is part of a growing movement toward greater accessibility to clinical trial information, prompted in part by high-profile cases involving the suppression of data by pharmaceutical companies.

In the European Union, all clinical trials conducted in member states are required to be registered in the EudraCT database, supervised by the European Medicines Agency.

In the United States, www.ClinicalTrials.gov

The WHO has acknowledged the need to balance increased transparency with the protection of competitive advantage. It may come down to a question of the timing of disclosure. In comments submitted to a WHO formal consultation on disclosure timing policy in April, the Pharmaceutical Research and Manufacturers of America noted “there may be infrequent instances where companies may regard certain data elements as sensitive for competitive reasons and wish to delay public disclosure.” In particular, the organization said that companies may wish to delay the disclosure of the official scientific title of the study, specific mechanism or molecular identifiers of the intervention, target sample size, primary outcome, and key secondary outcomes.

The WHO Registry Platform is expected to launch a Web-based search portal later this year that would allow interested individuals to search among participating registries for clinical trials taking place or completed throughout the world.

For more information on the registry platform, visit www.who.int/ictrp/en

Recommended Reading

ACP Proposes Pay Changes, Training Program Redesign
MDedge Rheumatology
Policy & Practice
MDedge Rheumatology
New Orleans' Medical Schools Awash in Optimism : Tulane and LSU report more candidates that have done charity work in the U.S. and other countries.
MDedge Rheumatology
NHMA Aims to Train Hispanic Physician Leaders
MDedge Rheumatology
Non-Hospital MDs Should Be at Forefront of Pandemic Flu Plan
MDedge Rheumatology
Government Offers Two Ways to Serve During Emergencies
MDedge Rheumatology
Plan Now to Use Telemedicine After Disaster Hits
MDedge Rheumatology
Feds Approve One Drug Assistance Program Redesign
MDedge Rheumatology
Policy & Practice
MDedge Rheumatology
Physicians Heed the Call To Adopt Health Care IT
MDedge Rheumatology