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4.
Hastings Cent Rep ; 49(2): 26-36, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30998281

RESUMO

Policy-makers, bioethicists, and patient advocates have been engaged in a fierce battle about the merits and potential harms of a federal right-to-try law. This debate about access to investigational medical products has raised profound questions about the limits of patient autonomy, appropriate government regulation, medical paternalism, and political rhetoric. For example, do patients have a right to access investigational therapies, as the right-to-try movement asserts? What is government's proper role in regulating and facilitating access to drugs that are still in development? In this review, we analyze the history of the right-to-try movement, review the arguments put forth by supporters and opponents of the legislation, and consider the movement's consequences. Two possible scenarios may emerge. One is that the right-to-try pathway may fail to meaningfully increase patient access to investigational products. Alternatively, certain companies may attempt to rely on the federal right-to-try legislation to sell investigational products, taking advantage of the provision that allows for direct costs, as there is currently no clear mechanism for enforcement or monitoring of cost calculations.


Assuntos
Drogas em Investigação , Aplicação de Novas Drogas em Teste/legislação & jurisprudência , Produção de Droga sem Interesse Comercial/legislação & jurisprudência , Defesa do Paciente/legislação & jurisprudência , Regulamentação Governamental , Acessibilidade aos Serviços de Saúde/legislação & jurisprudência , Humanos , Doente Terminal/legislação & jurisprudência , Estados Unidos , United States Food and Drug Administration/legislação & jurisprudência
5.
J Law Med Ethics ; 47(4): 732-747, 2019 12.
Artigo em Inglês | MEDLINE | ID: mdl-31957586

RESUMO

In the U.S., there is no requirement for research sponsors to compensate human research subjects who experience injuries as a result of their participation. In this article, we review the moral justifications that compel the establishment of a better research-related injury compensation system. We explore how other countries and certain institutions within the U.S. have adopted various systems of compensation. The existence of these systems demonstrates both that the U.S. lags behind other nations in its protection of human research subjects and that the establishment of a compensation system is both practical and feasible. We then examine factors which have prevented the U.S. from establishing its own compensation system. We consider possible alternatives for the U.S. by examining the advantages and disadvantages of both established and proposed systems. We offer a new proposal that addresses the justice concerns which compel the establishment of a national compensation system, distributes the burdens of such a system on multiple stakeholders that benefit from research, and has the additional advantage of minimizing the administrative and logistical challenges associated with initiating such a system.


Assuntos
Compensação e Reparação/ética , Experimentação Humana/ética , Experimentação Humana/legislação & jurisprudência , Ferimentos e Lesões/economia , Pesquisa Biomédica/organização & administração , Humanos , Índia , Seguro Saúde/organização & administração , Federação Russa , África do Sul , Estados Unidos
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