Aug 2026· Therapeutic Innovation and Regulatory Science· 0 citations· 11 references
Medicine
TL;DR
Describing trends in the geographic distribution of select measures of biopharmaceutical leadership from 2004 through 2024 suggests that over several decades, there has been a strong decline in European measures of leadership.
Abstract
For several decades, the United States (U.S.) has been the leader in biopharmaceutical advancements. Recently, the U.S. has increased government interventions to limit prices for patent-protected medicines. While it is unclear whether ongoing efforts to implement international reference pricing in the U.S. could have similar effects, descriptive measures of global biopharmaceutical market dynamics can help benchmark future assessments. In this analysis, we analyzed trends in the geographic distribution of select measures of biopharmaceutical leadership from 2004 through 2024. Using the PharmaProjects database from Citeline, we found that 43.1% of first launches of small-molecule and biologic drugs occurred in the U.S., 15.3% occurred in Europe, and 9.9% occurred in China. Over this time, the share of drugs launched first in the U.S. went from 45.9 to 37.8%, the share of drugs launched first in Europe fell from 26.7 to 8.5%, while this share in China grew from 3.3 to 28.7%. The share of first-launched therapeutics developed by U.S.-headquartered companies and by companies based in Europe declined while the share developed by companies based in China increased. Though additional research is needed on the measurement of biopharmaceutical leadership, and impacts of government intervention, this descriptive study suggests that over several decades, there has been a strong decline in European measures of leadership. At the same time, China is becoming increasingly important in the global biopharmaceutical space. This analysis supports the view that the U.S remains a leader, and offers a benchmark and context for future evaluations that consider potential unintended consequences of ongoing proposals to increase government intervention in the prices of patent-protected medicines.
Background The 21st Century Cures Act (2017) was enacted during a period of evolving FDA flexibility in evidentiary standards for drug approval. To examine trends before and after implementation, we independently reviewed all novel drugs approved between 2016 and 2024. Methods We constructed a database of all novel FDA...
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