Literature DB >> 15742586

The challenge of assuring continued post-trial access to beneficial treatment.

Christine Grady1.   

Abstract

Keywords:  Biomedical and Behavioral Research; Health Care and Public Health

Mesh:

Substances:

Year:  2005        PMID: 15742586

Source DB:  PubMed          Journal:  Yale J Health Policy Law Ethics        ISSN: 1535-3532


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  12 in total

1.  Ethical issues in HIV prevention research with people who inject drugs.

Authors:  Jeremy Sugarman; Scott M Rose; David Metzger
Journal:  Clin Trials       Date:  2013-10-14       Impact factor: 2.486

2.  Ethical issues for control-arm patients after revelation of benefits of experimental therapy: a framework modeled in neuroblastoma.

Authors:  Yoram Unguru; Steven Joffe; Conrad V Fernandez; Alice L Yu
Journal:  J Clin Oncol       Date:  2013-01-07       Impact factor: 44.544

Review 3.  Human dignity as a basis for providing post-trial access to healthcare for research participants: a South African perspective.

Authors:  Pamela Andanda; Jane Wathuta
Journal:  Med Health Care Philos       Date:  2018-03

4.  Access to medications and medical care after participation in HIV clinical trials: a systematic review of trial protocols and informed consent documents.

Authors:  Andrea L Ciaranello; Rochelle P Walensky; Paul E Sax; Yuchiao Chang; Kenneth A Freedberg; Joel S Weissman
Journal:  HIV Clin Trials       Date:  2009 Jan-Feb

5.  Subjects' views of obligations to ensure post-trial access to drugs, care and information: qualitative results from the Experiences of Participants in Clinical Trials (EPIC) study.

Authors:  N Sofaer; C Thiessen; S D Goold; J Ballou; K A Getz; G Koski; R A Krueger; J S Weissman
Journal:  J Med Ethics       Date:  2009-03       Impact factor: 2.903

6.  Forms of benefit sharing in global health research undertaken in resource poor settings: a qualitative study of stakeholders' views in Kenya.

Authors:  Geoffrey M Lairumbi; Michael Parker; Raymond Fitzpatrick; Michael C English
Journal:  Philos Ethics Humanit Med       Date:  2012-01-17       Impact factor: 2.464

7.  Reasons Why Post-Trial Access to Trial Drugs Should, or Need not be Ensured to Research Participants: A Systematic Review.

Authors:  Neema Sofaer; Daniel Strech
Journal:  Public Health Ethics       Date:  2011-07-11       Impact factor: 1.940

8.  Reciprocity-based reasons for benefiting research participants: most fail, the most plausible is problematic.

Authors:  Neema Sofaer
Journal:  Bioethics       Date:  2013-12-06       Impact factor: 1.898

9.  Incorporating ethical principles into clinical research protocols: a tool for protocol writers and ethics committees.

Authors:  Rebecca H Li; Mary C Wacholtz; Mark Barnes; Liam Boggs; Susan Callery-D'Amico; Amy Davis; Alla Digilova; David Forster; Kate Heffernan; Maeve Luthin; Holly Fernandez Lynch; Lindsay McNair; Jennifer E Miller; Jacquelyn Murphy; Luann Van Campen; Mark Wilenzick; Delia Wolf; Cris Woolston; Carmen Aldinger; Barbara E Bierer
Journal:  J Med Ethics       Date:  2016-01-25       Impact factor: 2.903

10.  The 'experimental public' in longitudinal health research: views of local leaders and service providers in rural South Africa.

Authors:  Rhian Twine; Gillian Lewando Hundt; Kathleen Kahn
Journal:  Glob Health Res Policy       Date:  2017-09-06
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