Literature DB >> 15994362

Stopping trials early for commercial reasons: the risk-benefit relationship as a moral compass.

A S Iltis1.   

Abstract

Decisions by industry sponsors to end clinical trials early for commercial reasons have been the subject of controversy. I argue that the principal consideration in assessing these decisions ought to be the way in which the termination would affect the trial's risk-benefit relationship. If there is not yet sufficient benefit to be gained from the study to offset the risks to which participants were exposed and it is expected that important scientific information would be obtained if the trial were continued, early termination constitutes an unethical alteration of the risk-benefit relationship. This violates the grounds on which permission is given to conduct human research, patients consent to participate, and investigators agree to conduct studies. These knowable and avoidable changes in risk-benefit relationship should generally be seen as impermissible.

Entities:  

Keywords:  Analytical Approach; Biomedical and Behavioral Research

Mesh:

Year:  2005        PMID: 15994362      PMCID: PMC1734192          DOI: 10.1136/jme.2004.008771

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  9 in total

Review 1.  Premature discontinuation of clinical trial for reasons not related to efficacy, safety, or feasibility.

Authors:  M Lièvre; J Ménard; E Bruckert; J Cogneau; F Delahaye; P Giral; E Leitersdorf; G Luc; L Masana; P Moulin; P Passa; D Pouchain; G Siest
Journal:  BMJ       Date:  2001-03-10

2.  Societal responsibilities of clinical trial sponsors. Lack of commercial pay off is not a legitimate reason for stopping a trial.

Authors:  S Evans; S Pocock
Journal:  BMJ       Date:  2001-03-10

3.  Responsibilities of sponsors are limited in premature discontinuation of trials.

Authors:  R Ashcroft
Journal:  BMJ       Date:  2001-07-07

4.  Stopping medical research to save money: a broken pact with researchers and patients.

Authors:  Bruce M Psaty; Drummond Rennie
Journal:  JAMA       Date:  2003 Apr 23-30       Impact factor: 56.272

5.  Early closure of European Pimagedine trial. Steering Committee. Safety Committee.

Authors:  G Viberti; G Slama; G Pozza; A Czyzyk; R W Bilous; A Gries; H Keen; J H Fuller; G Menzinger
Journal:  Lancet       Date:  1997-07-19       Impact factor: 79.321

6.  Early stopping of trials.

Authors:  G Hopf
Journal:  Lancet       Date:  1997-09-20       Impact factor: 79.321

7.  Early stopping of trials.

Authors:  A Langer
Journal:  Lancet       Date:  1997-09-20       Impact factor: 79.321

8.  Risk and medical ethics.

Authors:  E Pochin
Journal:  J Med Ethics       Date:  1982-12       Impact factor: 2.903

9.  Principal results of the Controlled Onset Verapamil Investigation of Cardiovascular End Points (CONVINCE) trial.

Authors:  Henry R Black; William J Elliott; Gregory Grandits; Patricia Grambsch; Tracy Lucente; William B White; James D Neaton; Richard H Grimm; Lennart Hansson; Yves Lacourciere; James Muller; Peter Sleight; Michael A Weber; Gordon Williams; Janet Wittes; Alberto Zanchetti; Robert J Anders
Journal:  JAMA       Date:  2003 Apr 23-30       Impact factor: 56.272

  9 in total
  6 in total

1.  Risk-benefit analysis: from a logical point of view.

Authors:  Georg Spielthenner
Journal:  J Bioeth Inq       Date:  2012-03-21       Impact factor: 1.352

2.  Wrongful termination: lessons from the Geron clinical trial.

Authors:  Christopher Thomas Scott; David Magnus
Journal:  Stem Cells Transl Med       Date:  2014-10-08       Impact factor: 6.940

3.  Would tirofiban have been shown non-inferior to abciximab had the TENACITY trial not been terminated for financial reasons?

Authors:  Peter B Berger; Judson B Williams; Vic Hasselblad; Karen Chiswell; Karen S Pieper; Robert M Califf
Journal:  J Interv Cardiol       Date:  2013-02-05       Impact factor: 2.279

4.  Quantitative Framework for Retrospective Assessment of Interim Decisions in Clinical Trials.

Authors:  Roger Stanev
Journal:  Med Decis Making       Date:  2016-06-27       Impact factor: 2.583

5.  Implications of product withdrawal on a post-approval pragmatic trial: The VOLUME study experience.

Authors:  Francesca M Kolitsopoulos; Nicolle M Gatto; Kevin Sweetland; Michael B Bracken; Neville Jackson
Journal:  Contemp Clin Trials Commun       Date:  2019-10-28

6.  Practices and Attitudes of Swiss Stakeholders Regarding Investigator-Initiated Clinical Trial Funding Acquisition and Cost Management.

Authors:  Stuart McLennan; Alexandra Griessbach; Matthias Briel
Journal:  JAMA Netw Open       Date:  2021-06-01
  6 in total

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