An analysis of common ethical justifications for compassionate use programs for experimental drugs

Kasper Raus1,2

  • 1Department of Philosophy and Moral Sciences, Ghent University, Ghent, Belgium. Kasper.Raus@UGent.be.

BMC Medical Ethics
|October 21, 2016
PubMed
Abstract

Insights

Terminally ill patients may access experimental drugs through expanded access programs, but current justifications based on justice, beneficence, and autonomy are problematic. These programs require redesign to truly maximize these ethical principles for patient benefit.

Area of Science:

  • Medical Ethics
  • Clinical Pharmacology
  • Patient Advocacy

Background:

  • New drug development involves lengthy clinical trials, delaying access for terminally ill patients.
  • Expanded access (compassionate use) programs offer pre-market experimental drugs to patients with life-threatening conditions.
  • Participation in randomized controlled trials (RCTs) is limited for terminally ill patients, with risks of exploitation.

Purpose of the Study:

  • To examine common ethical justifications for expanded access programs.
  • To critically analyze the ethical underpinnings of compassionate use.
  • To propose improvements for designing these programs.

Main Methods:

  • Analysis of ethical principles: justice, beneficence, and autonomy.
  • Review of existing justifications for expanded access programs.
  • Ethical argumentation regarding program design.

Main Results:

  • Common justifications for expanded access programs fall into three categories: justice, beneficence, and autonomy.
  • Each justification is found to be potentially problematic in its current application.
  • Current programs may not fully realize the ethical ideals they purport to uphold.

Conclusions:

  • Expanded access programs require a re-evaluation of their ethical foundations.
  • To be ethically sound, these programs must be designed to actively maximize justice, beneficence, and patient autonomy.
  • A more robust framework is needed to ensure equitable and ethical access to experimental therapeutics.

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