HealthDay News — Greater transparency is being urged in clinical research, according to a health policy brief published in Health Affairs.
Elizabeth Richardson, from the Brookings Center for Health Policy in Washington, D.C., discusses policy initiatives that focus on improving the use of clinical research for patients, providers, and health systems.
Richardson notes that in recent years there have been renewed efforts to improve transparency and access to trial data. Benefits of making these data available include allowing future researchers to learn from past failures and facilitating third-party reanalysis of data.
Organizations are supporting improved transparency, including the AllTrials campaign, the World Health Organization, and the European Medicines Agency. The U.S. Food and Drug Administration has taken some steps to share data more broadly, while other U.S.-based organizations have been more proactive, including the Institute of Medicine, Department of Health and Human Services, and several drug companies. The move toward greater transparency is not limited to medication trials but includes other interventions such as psychosocial and behavioral.
“In the near term, legislative efforts by the U.S. government are under way to improve clinical trial data sharing,” Richardson writes. “Over the longer term, it is unclear how the existing and emerging data-sharing initiatives will evolve, and their ultimate usefulness will depend on a range of issues that are still under discussion.”
Richardson E. Health Policy Brief: Transparency in Clinical Research. Health Affairs. January 14, 2016. http://healthaffairs.org/healthpolicybriefs/brief.php?brief_id=150