Keywords
AlternativesCancer
Case Studies
Consent
Disclosure
Disease
Drug Industry
Drugs
Human Experimentation
Industry
Informed Consent
Life
Moral Obligations
Patients
Physicians
Prognosis
Quality of Life
Random Selection
Research
Research Design
Research Subjects
Risks and Benefits
Terminally Ill
Therapeutic Research
Toxicity
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http://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=When+Research+Is+Best+Therapy.+&title=Hastings+Center+Report.+&volume=18&issue=2&pages=24-26&date=1988&au=Marquis,+Donhttp://hdl.handle.net/10822/731990
Abstract
A case study is presented in which a physician must decide whether to ask a renal cell carcinoma patient, who has declined treatment unless it would improve his quality of life or extend his period of survival, to participate in a study comparing a standard progestational agent (Depo-provera) with an otherwise unavailable drug (gamma-interferon) which offers the only promising treatment for his disease. Two commentaries weigh the moral obligations of the physician, the patient, and the drug company in a circumstance where the patient has the right to withdraw from the study if he is randomly chosen to receive the less effective drug. (KIE abstract)Date
2015-05-05Identifier
oai:repository.library.georgetown.edu:10822/731990Hastings Center Report. 1988 Apr/May; 18(2): 24-26.
0093-0334
http://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=When+Research+Is+Best+Therapy.+&title=Hastings+Center+Report.+&volume=18&issue=2&pages=24-26&date=1988&au=Marquis,+Don
http://hdl.handle.net/10822/731990
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