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Published on: December 11, 2016
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.
Background:
When a new intervention or drug is developed, this has to pass through various phases of clinical testing before it achieves market approval, which can take many years. This raises an issue for drugs which could benefit terminally ill patients. These patients might set their hopes on the experimental drug but are unable to wait since they are likely to pass away before the drug is available. As a means of nevertheless getting access to experimental drug, many seriously ill and terminally ill patients are therefore very willing to participate in randomised controlled trials. However, only very few terminally ill patients are able to actually participate, and those that do participate are at risk of participating solely as a way of getting experimental drugs. Currently, there are, however, ways of getting access to drugs that have not (yet) gained market approval. One such mean is via expanded access or compassionate use programs where terminally ill patients receive experimental new drugs that are not yet market approved. In this paper, I examine some of the common justifications for such programs.
Main Body:
The most frequently voiced justifications for compassionate use or expanded access programs could be put in one of three categories. First, there are justifications of justice, where compassionate use programs could be seen as a just or fair way to distribute experimental new drugs to patients who are denied access to RCT's through no fault of their own. Second, such programs could be justified by reference to the ethical principle of beneficence where it could be claimed that terminally ill patients stand to benefit greatly at very little risk (as they are already dying). Third, there are considerations of autonomy where, it is claimed, patients should be able to exercise their autonomy and have access to such drugs if that is there free choice and they are fully aware of the risks associated with that choice.
Short Conclusion:
In this paper, I argue currently all justifications are potentially problematic. If they truly form the basis for justification, compassionate use programs should be designed to maximize justice, beneficence and autonomy.
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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