Kesselheim AS - Clinical Pharmacology & Therapeutics
The Orphan Drug Act aims to advance therapeutic options for rare disease patients, but orphan drugs typically undergo more limited premarket testing than non-orphan drugs, resulting in greater clinical uncertainty. The authors argue that the ethical principles of justice and beneficence necessitate enhanced informed consent procedures for patients receiving orphan drugs and increased investment in postmarket surveillance and confirmatory testing.
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Daval CJR, Kesselheim AS - STAT
Mulsant SS, Kesselheim AS, Naci H - Journal of Cancer Policy
Avorn J - MedPage Today