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  Photo courtesy of Gabrielle Emanuel
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October 20-22, 2006, McShain Lounge, McCarthy Hall, Georgetown University, Washington, DC, USA


Medical researchers often discover that their subjects are afflicted with diseases and conditions other than the disease or condition under study. There is no settled ethical guidance on when medical researchers or research sponsors have a responsibility to provide “ancillary care”—care for these additional diseases or conditions. Drawing together bioethicists, medical researchers, legal experts, economists, and health policy experts from around the world, this workshop explored current ancillary-care practices and needs, debated alternative principled approaches to ancillary-care obligations, and examined the legal, economic, and policy issues pertaining to working out guidelines on this neglected topic in the ethics of medical research.

Consensus paper: With the participation of all but two of the workshop’s speakers (whose schedules did not permit them to participate), a paper expressing the consensus of the workshop has now been published in PLoS Medicine 5(5): e90 doi:10.1371/journal.pmed.0050090

Workshop speakers included:

Roger Brownsword, King’s College, London (UK)
Alexander M. Capron, University Professor, Scott H. Bice Chair in Healthcare Law, Policy and Ethics, and Professor of Law and Medicine at USC.
Richard Chaisson, MD, Professor and Director, Center for TB Research, Johns Hopkins University
Michael D. Clayman, Vice President, Lilly Research Laboratories (USA)
Peter B. Corr, PhD, Senior Vice President for Science and Technology, Pfizer Inc. (USA)
Stephen DeCherney, MD, MPG, President, Global Clinical Research Organization, Quintiles, Inc. (USA)
Christine Grady, PhD, RN, Department of Clinical Bioethics, NIH (USA) Elizabeth S. Higgs, MD, NIAID, NIH (USA)
Elizabeth S. Higgs, MD, MIA, DTM&H, Division of Clinical Research, NIAID, NIH
Dr. Nandini K. Kumar, Division of Basic Medical Sciences, Traditional Medicine and Bio-Medical Ethics, Indian Council of Medical Research
Reidar Lie, MD, PhD, Department of Clinical Bioethics, NIH (USA)
Maria Merritt, PhD, Berman Bioethics Institute, Johns Hopkins University (USA)
Prof. Malcolm Molyneux, Director, Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi
Beyene Petros, D.Sc., Associate Professor of Biomedical Sciences, Department of Biology, Addis Ababa University; member of the Council of People's Representatives (Ethiopia)
Henry S. Richardson, PhD, JD, MPP, Georgetown University (USA)
Jeremy Sugarman, MD, MPH, Professor of Bioethics and Medicine, Johns Hopkins University
Sandy Thomas, Executive Director, Nuffield Council (UK)

This Workshop was sponsored by the Reflective Engagement Initiative at Georgetown University, with additional support from Georgetown University's Department of Philosophy, the Kennedy Institute of Ethics, and the PhRMA Foundation.


 
Last update 10/19/06
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