Evidence map›Paper›PMID 42121240›Full record

ArticleGlobalization and health2026

Building a case for accelerated clinical development of drugs and vaccines - what are the driving forces?

Loïs C van Eck, Clàudia Pallisé Perelló, Natalie Evans, Mariëtte A van den Hoven, Martin P Grobusch, Sabine M Hermans, Hanna K de Jong

Abstract read
In one paragraph

Article in Globalization and health, 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

7 authors.

Loïs C van EckCenter for Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Amsterdam Institute for Immunology and Infectious Diseases, Amsterdam Public Health - Global Health, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.
Clàudia Pallisé PerellóDepartment of Ethics, Law and Humanities, Amsterdam Public Health Institute, Amsterdam UMC, Vrije University Amsterdam, de Boelelaan 1117, Amsterdam, 1081 HV, The Netherlands.
Natalie EvansDepartment of Ethics, Law and Humanities, Amsterdam Public Health Institute, Amsterdam UMC, Vrije University Amsterdam, de Boelelaan 1117, Amsterdam, 1081 HV, The Netherlands.
Mariëtte A van den HovenDepartment of Ethics, Law and Humanities, Amsterdam Public Health Institute, Amsterdam UMC, Vrije University Amsterdam, de Boelelaan 1117, Amsterdam, 1081 HV, The Netherlands.
Martin P GrobuschCenter for Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Amsterdam Institute for Immunology and Infectious Diseases, Amsterdam Public Health - Global Health, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.
Sabine M HermansCenter for Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Amsterdam Institute for Immunology and Infectious Diseases, Amsterdam Public Health - Global Health, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.
Hanna K de JongCenter for Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Amsterdam Institute for Immunology and Infectious Diseases, Amsterdam Public Health - Global Health, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands. h.k.dejong@amsterdamumc.nl.ORCID 0000-0001-6224-7947

Funding

Amsterdam Public Health Research Institute APH-GH-2021-2European Commission Grant Agreement no: 101058094
6 · The paper itself

Abstract

backgroundThe COVID-19 pandemic, among others, has shown the world that rapid drug and vaccine development and expedited clinical trials can be effective and safe. The overall benefit of accelerating clinical development would be faster public access to medicines. In this study, we explore key stakeholders' experiences and perceptions of drivers for the acceleration of clinical development.

methodsWe conducted semi-structured interviews with policy advisors and experts from key stakeholder groups involved in clinical development, identified via a power-interest stakeholder analysis. Thematic analysis was used to identify analytic themes.

resultsTwenty-five participants were interviewed representing pharmaceutical companies, the European Medicines Agency, national competent authorities in the EU, different research and clinical development organizations, including non-governmental organizations, and the World Health Organization. Drivers facilitating acceleration of clinical development could be grouped into three themes: alignment of stakeholders, innovative research design and processes, and financing. Some barriers of systematic acceleration were raised within these themes: European disharmony in trials practice, regulations and guidance; fragmentation of efforts; bureaucracy and the complexity of the Clinical Trials Information System (CTIS) submission process; and financial neglect for poverty-related diseases.

conclusionTo sustainably accelerate clinical development, future policies should facilitate collaboration and communication between stakeholders and work to minimize technical and bureaucratic barriers.

Indexed as

COVID-19 VaccinesDrug DevelopmentVaccinesClinical Trials as TopicCOVID-19HumansInterviews as TopicStakeholder ParticipationCOVID-19 VaccinesVaccines

Identifiers

PMID42121240
PMCPMC13169579

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.