Evidence map›Paper›PMID 39702219›Full record

ArticleOrphanet journal of rare diseases2024

Multi-stakeholder sessions on major innovation topics in rare disease clinical trials.

Daniel Bodden, Stefanie Schoenen, Stephanie Wied, Johan Verbeeck, Maya Dirani, Hiba Abou Daya, Nicole Heussen, Geert Molenberghs, Ralf-Dieter Hilgers, Rima Nabbout

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Daniel BoddenInstitute of Medical Statistics, RWTH Aachen University Aachen, Pauwelsstrasse 19, 52064, Aachen, Germany. daniel.bodden@rwth-aachen.de.ORCID 0000-0003-1051-5713
Stefanie SchoenenInstitute of Medical Statistics, RWTH Aachen University Aachen, Pauwelsstrasse 19, 52064, Aachen, Germany.
Stephanie WiedInstitute of Medical Statistics, RWTH Aachen University Aachen, Pauwelsstrasse 19, 52064, Aachen, Germany.
Johan VerbeeckI-BioStat, Data Science Institute, Hasselt University, Martelarenlaan 42, 3500, Hasselt, Belgium.
Maya DiraniInstitut des Maladies Gènètiques Imagine- Necker Enfants malades Hospital, 24 Boulevard du Montparnasse, 75015, Paris, France.
Hiba Abou DayaThematic Institute of Genetics, Genomics & Bioinformatics, INSERM, 8 rue de la Croix Jarry, 75013, Paris, France.
Nicole HeussenInstitute of Medical Statistics, RWTH Aachen University Aachen, Pauwelsstrasse 19, 52064, Aachen, Germany.
Geert MolenberghsI-BioStat, Data Science Institute, Hasselt University, Martelarenlaan 42, 3500, Hasselt, Belgium.
Ralf-Dieter HilgersInstitute of Medical Statistics, RWTH Aachen University Aachen, Pauwelsstrasse 19, 52064, Aachen, Germany.
Rima NabboutInstitut des Maladies Gènètiques Imagine- Necker Enfants malades Hospital, 24 Boulevard du Montparnasse, 75015, Paris, France.

Funding

Horizon 2020 825575
6 · The paper itself

Abstract

backgroundThe European Joint Programme on Rare Diseases aims to enhance the rare diseases research ecosystem by bringing together stakeholders such as research funders, institutions and patient organizations. Work Package 20 focuses on the validation, use and development of innovative methodologies for rare disease clinical trials. This paper reports on the outcomes of a retreat held in April 2023, where areas for innovation and educational needs in rare disease clinical trials were discussed in multi-stakeholder sessions.

methodsMulti-stakeholder sessions covered the topics: Future Educational System, Randomization in Rare Disease Clinical Trials, Endpoints in Rare Disease Clinical Trials and Using History Course Data. The sessions began with expert presentations to set the scene, followed by guided discussions facilitated by questions on a collaborative digital whiteboard. Participants wrote responses, which were then discussed live with the experts.

resultsTraining is needed for diverse stakeholders in rare disease clinical trials to enhance understanding and drive innovation. Challenges include a lack of standardized terminology for multiple endpoints, inadequate understanding of randomization in small sample studies and various obstacles in effectively using natural history data.

conclusionCreating a comprehensive and sustainable educational program for rare diseases clinical trial methodology requires strategic collaboration and adherence to FAIR principles. The workshop highlighted the need for innovations for topics in areas such as handling missing data, optimizing the extraction of information from small samples, remote endpoint measurement and new randomized inference techniques. Additionally, integrating innovations into tailored training programs is crucial for advancing the field.

Indexed as

Clinical Trials as TopicRare DiseasesHumansEducational systemFinite populationsMultiple endpointsNatural historyRandomization

Identifiers

PMID39702219
PMCPMC11657468

What OpenQuestion holds

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LicenceCC BY
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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.