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Why restrict medical effective altruism?
1Department of Philosophy, University of Arizona, Tucson, Arizona, USA.
Challenge trials involve purposefully exposing volunteers to pathogens to test treatments. This study argues that comparing research risks to societal risks, like military service, suggests no limit on acceptable volunteer risks.
Area of Science:
- Bioethics
- Medical Research Ethics
- Public Health
Background:
- Challenge trials involve controlled pathogen exposure to test medical interventions.
- Medical effective altruism (MEA) describes individuals volunteering for public good, accepting risks.
- Bioethicists raised ethical objections to challenge trials, particularly during COVID-19 vaccine development.
Purpose of the Study:
- To critically evaluate the ethical permissibility of risks undertaken by research subjects in challenge trials.
- To address the lack of a clear framework for judging acceptable harm levels in research.
- To examine Alex London's social consistency test for research risks.
Main Methods:
- Analysis of bioethical objections to challenge trials.
- Evaluation of Alex London's social consistency test for research risks.
- Comparison of risks in challenge trials to risks accepted in other societal spheres, specifically volunteer military service.
Main Results:
- The study concludes that the core ethical issue in challenge trials is determining permissible risk levels for subjects.
- Applying the social consistency test, particularly by comparing research risks to those in volunteer military service, suggests no inherent cap on acceptable risks.
- This implies that if societal norms permit soldiers to accept high risks, similar acceptance may extend to research volunteers.
Conclusions:
- The social consistency test, when applied broadly, does not provide a definitive limit on acceptable risks in challenge trials.
- Volunteer military service serves as a relevant social comparison, indicating that research volunteers could permissibly accept significant risks.
- Further development of ethical frameworks is needed to establish clear guidelines for risk assessment in human subject research.
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