Right to Experimental Treatment: FDA New Drug Approval, Constitutional Rights, and the Public's Health
On May 2, 2006, a divided panel of the U.S. Court of Appeals for the District of Columbia, in a startling opinion, Abigail Alliance for Better Access to Developmental Drugs v. Eschenbach, held that terminally ill patients who have exhausted all other available options have a constitutional right to...
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Veröffentlicht in: | The Journal of law, medicine & ethics medicine & ethics, 2009-06, Vol.37 (2), p.269-279 |
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description | On May 2, 2006, a divided panel of the U.S. Court of Appeals for the District of Columbia, in a startling opinion, Abigail Alliance for Better Access to Developmental Drugs v. Eschenbach, held that terminally ill patients who have exhausted all other available options have a constitutional right to experimental treatment that FDA has not yet approved. Although ultimately overturned by the full court, Abigail Alliance generated considerable interest from various constituencies. Meanwhile, FDA proposed similar regulatory amendments, as have lawmakers on both sides of the aisle in Congress. But proponents of expanded access fail to consider public health and consumer safety concerns. In particular, allowing patients to try unproven treatments, outside of controlled clinical trials risks both the study's outcome and the health of patients who might benefit from the deliberate, careful process of new drug approval as it currently operates under FDA's auspices. |
doi_str_mv | 10.1111/j.1748-720X.2009.00371.x |
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Eschenbach, held that terminally ill patients who have exhausted all other available options have a constitutional right to experimental treatment that FDA has not yet approved. Although ultimately overturned by the full court, Abigail Alliance generated considerable interest from various constituencies. Meanwhile, FDA proposed similar regulatory amendments, as have lawmakers on both sides of the aisle in Congress. But proponents of expanded access fail to consider public health and consumer safety concerns. In particular, allowing patients to try unproven treatments, outside of controlled clinical trials risks both the study's outcome and the health of patients who might benefit from the deliberate, careful process of new drug approval as it currently operates under FDA's auspices.</description><identifier>ISSN: 1073-1105</identifier><identifier>EISSN: 1748-720X</identifier><identifier>DOI: 10.1111/j.1748-720X.2009.00371.x</identifier><identifier>PMID: 19493072</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject><![CDATA[Alliances ; Clinical trials ; Compassionate Use Trials - legislation & jurisprudence ; Constitutional rights ; Courts ; Drug and Narcotic Control - legislation & jurisprudence ; Drug approval ; Drugs ; Drugs, Investigational - supply & distribution ; Due process of law ; FDA approval ; Food ; Government regulation ; Government regulation of business ; Health Services Accessibility - ethics ; Health Services Accessibility - legislation & jurisprudence ; Health technology assessment ; Humans ; Laws, regulations and rules ; Medical treatment ; Patient Rights - ethics ; Patient Rights - legislation & jurisprudence ; Pharmaceutical research ; Public health ; State court decisions ; Terminal illnesses ; Terminally ill ; Terminally Ill - legislation & jurisprudence ; United States ; United States Food and drug administration]]></subject><ispartof>The Journal of law, medicine & ethics, 2009-06, Vol.37 (2), p.269-279</ispartof><rights>2009 American Society of Law, Medicine & Ethics</rights><rights>2009 American Society of Law, Medicine & Ethics, Inc.</rights><rights>COPYRIGHT 2009 Sage Publications, Inc.</rights><rights>Copyright © American Society of Law, Medicine and Ethics 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c8081-3db185c7b7de56794ee5645bc329a3aea099a1cbb6cdf08d55fa6a4c62acd0a93</citedby><cites>FETCH-LOGICAL-c8081-3db185c7b7de56794ee5645bc329a3aea099a1cbb6cdf08d55fa6a4c62acd0a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1748-720X.2009.00371.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1748-720X.2009.00371.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27864,27865,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19493072$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leonard, Elizabeth Weeks</creatorcontrib><title>Right to Experimental Treatment: FDA New Drug Approval, Constitutional Rights, and the Public's Health</title><title>The Journal of law, medicine & ethics</title><addtitle>J Law Med Ethics</addtitle><description>On May 2, 2006, a divided panel of the U.S. Court of Appeals for the District of Columbia, in a startling opinion, Abigail Alliance for Better Access to Developmental Drugs v. Eschenbach, held that terminally ill patients who have exhausted all other available options have a constitutional right to experimental treatment that FDA has not yet approved. Although ultimately overturned by the full court, Abigail Alliance generated considerable interest from various constituencies. Meanwhile, FDA proposed similar regulatory amendments, as have lawmakers on both sides of the aisle in Congress. But proponents of expanded access fail to consider public health and consumer safety concerns. In particular, allowing patients to try unproven treatments, outside of controlled clinical trials risks both the study's outcome and the health of patients who might benefit from the deliberate, careful process of new drug approval as it currently operates under FDA's auspices.</description><subject>Alliances</subject><subject>Clinical trials</subject><subject>Compassionate Use Trials - legislation & jurisprudence</subject><subject>Constitutional rights</subject><subject>Courts</subject><subject>Drug and Narcotic Control - legislation & jurisprudence</subject><subject>Drug approval</subject><subject>Drugs</subject><subject>Drugs, Investigational - supply & distribution</subject><subject>Due process of law</subject><subject>FDA approval</subject><subject>Food</subject><subject>Government regulation</subject><subject>Government regulation of business</subject><subject>Health Services Accessibility - ethics</subject><subject>Health Services Accessibility - legislation & 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subjects | Alliances Clinical trials Compassionate Use Trials - legislation & jurisprudence Constitutional rights Courts Drug and Narcotic Control - legislation & jurisprudence Drug approval Drugs Drugs, Investigational - supply & distribution Due process of law FDA approval Food Government regulation Government regulation of business Health Services Accessibility - ethics Health Services Accessibility - legislation & jurisprudence Health technology assessment Humans Laws, regulations and rules Medical treatment Patient Rights - ethics Patient Rights - legislation & jurisprudence Pharmaceutical research Public health State court decisions Terminal illnesses Terminally ill Terminally Ill - legislation & jurisprudence United States United States Food and drug administration |
title | Right to Experimental Treatment: FDA New Drug Approval, Constitutional Rights, and the Public's Health |
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