Evidence map›Paper›PMID 42496993›Full record

ArticleJAMA health forum2026

Clinical Development, Regulatory, and Reimbursement Review Duration of New Drugs in the US and European Countries.

Simon Hediger, Camille E G Glaus, Stacie B Dusetzina, Ulrich-Peter Rohr, Thomas J Hwang, Kerstin Noelle Vokinger

Abstract read
In one paragraph

Article in JAMA health forum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Simon HedigerAcademic Chair for Regulation in Law, Medicine, and Technology, University of Zurich, Zurich, Switzerland.
Camille E G GlausAcademic Chair for Regulation in Law, Medicine, and Technology, University of Zurich, Zurich, Switzerland.
Stacie B DusetzinaDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Ulrich-Peter RohrSwissmedic, Swiss Agency for Therapeutic Products, Bern, Switzerland.
Thomas J HwangProgram On Regulation, Therapeutics, and Law (PORTAL), Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Kerstin Noelle VokingerAcademic Chair for Regulation in Law, Medicine, and Technology, University of Zurich, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Rapid access to new drugs is of interest to patients and society. Objective: To analyze duration for clinical development, regulatory review, and reimbursement review of new drugs and assess whether these durations changed over the past decade in the US and European countries (Germany, France, and Switzerland). Design, Setting, and Participants: In this cross-sectional study, databases of the US Food and Drug Administration, the European Medicines Agency, and the Swiss Agency for Therapeutic Products were used to identify all new drugs approved from 2014 to 2024, investigational new drug application dates, submission dates, and approval pathways. Reimbursement dates were extracted from Medicare (US), Ministry of Health and Prevention (France), Federal Joint Committee (Germany), Federal Office of Public Health (Switzerland). Main Outcomes and Measures: Kaplan-Meier estimates were applied to calculate the median time for clinical development, regulatory review, and reimbursement review. Results: This study included 519 drugs in the US, 412 in France, 412 in Germany, and 395 in Switzerland. Median total duration from clinical trial initiation until reimbursement was 9.3 (95% CI, 9.0-9.8) years in the US, 11.1 (95% CI, 10.2-12.0) years in France, 8.9 (95% CI, 8.3-9.5) years in Germany, and 9.8 (95% CI, 9.6-10.5) years in Switzerland. Median total duration from clinical trial initiation until reimbursement increased in the US from 9.0 (95% CI, 8.43-9.90) years in the first period (January 2014-August 2017) to 9.35 (95% CI, 8.75-11.56) years in the most recent period (May 2021-December 2024). In France, the median total duration increased from 9.82 (95% CI, 8.88-11.41) years to 12.18 (95% CI, 10.12-14.78) years. In Switzerland, median total duration increased from 9.42 (95% CI, 8.2-10.17) years to 10.05 (95% CI, 9.39-12.32) years. In Germany, the median total duration decreased from 9.27 (95% CI, 7.67-10.6) years to 8.7 (95% CI, 7.92-9.57) years. Cancer drugs showed a shorter median total duration compared with all drugs, especially in the US and Germany, and less pronounced in Switzerland and France. Conclusions and Relevance: The findings of this study suggest that the overall median duration from clinical development until reimbursement of new drugs showed only minimal variation over time. Given recent efforts to accelerate new drug approvals, future research should evaluate potentially modifiable factors that increase clinical development durations. This could help to better target policies to accelerate access to new drugs, ideally adequately balancing safety with speed.

Indexed as

Drug ApprovalDrug DevelopmentReimbursement MechanismsCross-Sectional StudiesEuropeHumansSwitzerlandTime FactorsUnited StatesUnited States Food and Drug Administration

Identifiers

PMID42496993
PMCPMC13401199

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.