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  1. Fair Allocation of GLP-1 and Dual GLP-1-GIP Receptor Agonists.Ezekiel J. Emanuel, Johan L. Dellgren, Matthew S. McCoy & Govind Persad - forthcoming - New England Journal of Medicine.
    Glucagon-like peptide-1 (GLP-1) receptor agonists, such as semaglutide, and dual GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) receptor agonists, such as tirzepatide, have been found to be effective for treating obesity and diabetes, significantly reducing weight and the risk or predicted risk of adverse cardiovascular events. There is a global shortage of these medications that could last several years and raises questions about how limited supplies should be allocated. We propose a fair-allocation framework that enables evaluation of the ethics of current (...)
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  • Is Deidentification Sufficient to Protect Health Privacy in Research?Mark A. Rothstein - 2010 - American Journal of Bioethics 10 (9):3-11.
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  • Rethinking research ethics.Rosamond Rhodes - 2005 - American Journal of Bioethics 5 (1):7 – 28.
    Contemporary research ethics policies started with reflection on the atrocities perpetrated upoconcentration camp inmates by Nazi doctors. Apparently, as a consequence of that experience, the policies that now guide human subject research focus on the protection of human subjects by making informed consent the centerpiece of regulatory attention. I take the choice of context for policy design, the initial prioritization of informed consent, and several associated conceptual missteps, to have set research ethics off in the wrong direction. The aim of (...)
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  • Privacy Overkill.Rosamond Rhodes & Daniel A. Moros - 2010 - American Journal of Bioethics 10 (9):12-15.
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  • In defense of the duty to participate in biomedical research.Rosamond Rhodes - 2008 - American Journal of Bioethics 8 (10):37 – 38.
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  • Urge Overkill: Protecting Deidentified Human Subjects at What Price?Misha Angrist - 2010 - American Journal of Bioethics 10 (9):17-18.
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  • The Recipe for Overreaching Regulation.Abraham Schwab - 2010 - American Journal of Bioethics 10 (8):55-56.
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  • Balancing Privacy Protections with Efficient Research: Institutional Review Boards and the Use of Certificates of Confidentiality.Peter M. Currie - 2005 - IRB: Ethics & Human Research 27 (5):7.
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  • Informed Consent and Biobanks.Ellen Wright Clayton - 2005 - Journal of Law, Medicine and Ethics 33 (1):15-21.
    Biomedical research has always relied on access to human biological materials and clinical information, resources that when combined form biobanks. In the past, it appears that investigators sometimes used these resources with relatively little oversight, and without the consent of the individuals from whom these materials and information were obtained. Several developments in the last ten to fifteen years have converged to place greater emphasis on the role of individual consent in the creation and use of biobanks. The most important (...)
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  • “Human Non-Subjects Research”: Privacy and Compliance.Kyle Bertram Brothers & Ellen Wright Clayton - 2010 - American Journal of Bioethics 10 (9):15-17.
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