Drug pricing: why international reference may not work for the United States

A Value in Health commentary analyzes Europe’s experience with international reference pricing (IRP) and warns that a U.S. “Most-Favored Nation” model could restrict access to new medicines without ensuring sustainable price reductions.

Rafael Mantovani

5 min read

October 1, 2025

The U.S. government under President Trump proposed in 2025 a “Most-Favored Nation” (MFN) model, aiming to benchmark domestic drug prices against those in other developed countries through international reference pricing (IRP). However, a recent commentary in Value in Health argues that such an approach may create more harm than benefit.

In Europe, IRP delivered only short-term budget savings. Over time, list prices converged with those of high-income “anchor” countries such as Germany and France, without true long-term reductions. This mechanism also delayed or restricted access to innovative medicines in less affluent countries, forcing payers to adopt confidential, non-transparent pricing agreements with manufacturers.

According to the authors, implementing MFN in the U.S. could make the country the new global reference point for drug prices. This shift may drive pharmaceutical companies to set even higher launch prices to offset potential revenue losses. Such dynamics risk undermining incentives for innovation and worsening inequities in drug access worldwide.

As a more sustainable alternative, the commentary suggests that the U.S. should strengthen its own health technology assessment (HTA) frameworks. By systematically evaluating clinical benefit, cost-effectiveness, and societal willingness to pay, HTA mechanisms could offer more rational and predictable drug pricing decisions, avoiding the pitfalls observed in Europe.

Farmacoeconomics
Health Technology Assessement

Sources

  • Grueger J, Martin K, Sullivan SD. Referencing drug prices of other countries may not sustainably lower prices in the United States: lessons from Europe. Value Health. 2025;28(9):1305-8. doi:10.1016/j.jval.2025.06.010.

Written by Rafael Mantovani

About

Rafael Mantovani holds a Pharmacy degree and a Master’s in Pharmaceutical Sciences from the Federal University of São Paulo (UNIFESP). Over the course of his career, he has built solid expertise in Medical Affairs, working at the intersection of science, strategy, and medical education. His professional focus lies in evidence-based medicine and health technology assessment (HTA), with a strong commitment to translating data into meaningful decisions that benefit both patients and healthcare systems. With experience spanning Medical Information, Pharmacovigilance, and Medical Science Liaison roles, Rafael has developed a broad understanding of how science and innovation can be applied strategically. Currently serving as a Medical Affairs Manager, he leads teams and projects across different therapeutic areas, combining scientific rigor, engagement with key opinion leaders, and a clear vision for sustainable impact in healthcare.