From Research to Care: Modernizing U.S. Clinical Trial Infrastructure
The United States (U.S.) has long led the world in biomedical discovery, translation into clinical research, and approvals of new cures and life-changing treatments. But even as biomedical science accelerates the identification of these potentially transformative therapies, America’s clinical research enterprise is not keeping pace. Most clinical research in the U.S. remains fragmented and reliant on separate data, measurement, and process requirements that do not fit well into routine care. The resulting costs and burden of clinical research limit patient access and slow the generation of evidence needed to guide treatment.
Key actors in the biomedical innovation ecosystem are developing an increasingly rich array of public and private resources to address this critical challenge. Yet despite these efforts, clinical research integrated into care remains the exception, and other countries are more rapidly progressing to improve the speed and efficiency of both early-stage (e.g., Phase 1 clinical trials) and more advanced clinical development.
This draft framing report describes the current inefficiencies of U.S. clinical research, highlights the need for modernizing the U.S. clinical trial enterprise while also advancing early-stage drug development, and conceptualizes the next generation of drug development and regulation in the U.S. We propose a series of practical policy initiatives to further enable U.S. actions that advance the global use of aligned, modernized standards for clinical development across regulatory agencies.
Read the full document here.
Request for Comments
Duke-Margolis is seeking comments on this discussion draft, including but not limited to promising near-term opportunities for implementation of concepts described in this framework, and specific regulatory reforms and implementation supports which would advance the clinical development goals described in this discussion draft. Any responses received by June 15, 2026, would be particularly appreciated. For comments, please submit your responses via this form. Please email us at clinresearchcomments@duke.edu with any questions.
Duke-Margolis Authors
Valerie J. Parker, MSc
Assistant Policy Research Director, Regulatory & Real-World Data and Evidence
Brian Canter, PhD
Assistant Policy Research Director
Patrick Rodriguez, MA
Policy Analyst
2024 Margolis Intern
Marianne Hamilton Lopez, PhD, MPA
Senior Research Director, Biomedical Innovation
Faculty Director of the Duke-Margolis Postdoctoral Associates & Affiliated Fellows Program
Adjunct Associate Professor
Senior Team Member
Margolis Core Faculty
Mark McClellan, MD, PhD
Director of the Duke-Margolis Institute for Health Policy
Robert J. Margolis, MD, Professor of Business, Medicine and Policy
Margolis Executive Core Faculty