David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
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Bioethics 15 (4):312–332 (2001)
This paper examines the role of equipoise in evaluating international research. It distinguishes two possible formulations of the equipoise requirement that license very different evaluations of international research proposals. The interpretation that adopts a narrow criterion of similarity between clinical contexts has played an important role in one recent controversy, but it suffers from a number of problems. An alternative interpretation that adopts a broader criterion of similarity does a better job of avoiding both exploitation of the brute fact of social deprivation and the exploitation of needy populations for the benefit of more well-off populations. It also holds out the promise of reconciling the need to find interventions that can be employed in developing world contexts with the cluster of moral values that must constrain the way such research is carried out.
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Sven Ove Hansson (2004). Weighing Risks and Benefits. Topoi 23 (2):145-152.
Rieke van der Graaf & Johannes J. M. van Delden (2009). What is the Best Standard for the Standard of Care in Clinical Research? American Journal of Bioethics 9 (3):35 – 43.
Sven Ove Hansson (2010). Reversing “Research Exceptionalism”. American Journal of Bioethics 10 (8):66-67.
J. C. Lindsey, S. K. Shah, G. K. Siberry, P. Jean‐Philippe & M. J. Levin (2013). Ethical Tradeoffs in Trial Design: Case Study of an HPV Vaccine Trial in HIV‐Infected Adolescent Girls in Lower Income Settings. Developing World Bioethics 13 (2):95-104.
Rieke van Der Graaf & Johannes JM van Delden (2009). Response to Open Peer Commentaries on “What is The Best Standard for the Standard of Care in Clinical Research?”. American Journal of Bioethics 9 (6):7-8.
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