Evidence map›Paper›PMID 40249275›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2025

Treatment Selection and Prioritization for the EJS ACT-PD MAMS Trial Platform.

Cristina Gonzalez-Robles, Dilan Athauda, Thomas R Barber, Roger A Barker, David T Dexter, Susan Duty, Romy Ellis-Doyle, Sonia Gandhi, Joel Handley, Edwin Jabbari and 20 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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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

30 authors.

Cristina Gonzalez-RoblesDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.ORCID 0000-0001-6809-0127
Dilan AthaudaDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.ORCID 0000-0001-8594-2483
Thomas R BarberDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.
Roger A BarkerJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
David T DexterParkinson's UK, London, United Kingdom.
Susan DutyWolfson Sensory, Pain and Regeneration Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.ORCID 0000-0003-3408-5973
Romy Ellis-DoyleDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.
Sonia GandhiDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.
Joel HandleyNorth Bristol NHS Trust, Bristol, United Kingdom.
Edwin JabbariDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.ORCID 0000-0001-6844-882X
Keith MartinExpert Through Experience, London, United Kingdom.
Kevin McFarthingExpert Through Experience, London, United Kingdom.
Georgia MillsDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.
Heather MortiboysSheffield Institute for Translational Neuroscience, School of Medicine and Population Health, The University of Sheffield, Sheffield, United Kingdom.
Stephen MullinFaculty of Health, University of Plymouth, Plymouth, United Kingdom.
Rebecca PettyFaculty of Health, University of Plymouth, Plymouth, United Kingdom.
Esther SammlerMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.ORCID 0000-0003-3218-7116
Paula ScurfieldDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.
Simon R W StottCure Parkinson's, London, United Kingdom.
George K TofarisNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9252-5933
Li WeiResearch Department of Practice and Policy, School of Pharmacy, University College London, London, United Kingdom.
Caroline H Williams-GrayJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-2648-9743
Alan WongPharmacy Service, Royal Free Hospital NHS Foundation Trust, London, United Kingdom.
Marie-Louise ZeisslerFaculty of Health, University of Plymouth, Plymouth, United Kingdom.ORCID 0000-0002-6232-4284
Richard K WyseCure Parkinson's, London, United Kingdom.
Camille B CarrollFaculty of Health, University of Plymouth, Plymouth, United Kingdom.
Thomas FoltynieDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.ORCID 0000-0003-0752-1813
Oliver BandmannSheffield Institute for Translational Neuroscience, School of Medicine and Population Health, The University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0003-3149-0252
Anthony H V SchapiraDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom.
EJS ACT‐PD Consortium

Funding

Edmond J. Safra Philanthropic Foundation
6 · The paper itself

Abstract

backgroundThere are currently no disease-modifying therapies (DMTs) registered for Parkinson's disease (PD). The Edmond J. Safra Accelerating Clinical Trials in Parkinson Disease (EJS ACT-PD) initiative will expedite clinical assessment of putative DMTs through a multi-arm multistage (MAMS) trial, testing several treatments against a common placebo arm and replacing unsuccessful therapies early.

objectiveThe objective of this study was to describe the treatment selection process for the EJS ACT-PD clinical trial platform.

methodsA Treatment Selection Working Group (TSWG) identified compounds using complementary strategies, such as literature search, related initiatives (Cure Parkinson's International Linked Clinical Trials [iLCT] initiative), and expert suggestions. Compounds were classified into five mechanistic subgroups (mitochondrial, lysosomal, protein, inflammation, "other"). "Go/No-Go" criteria and a scoring system covering preclinical, pharmacological, and clinical evidence were devised. Experts scored the candidates for quantitative rankings. Dossiers adapted from iLCT documents were produced for the top-ranked compounds and in turn prioritized by the TSWG. Practical and logistical considerations from the Steering Committee (SC) guided the final decision. Patient and Public Involvement and Engagement representatives provided feedback throughout the process.

resultsA total of 293 interventions were identified, 52 of which passed the "Go/No-Go" criteria and were scored. Dossiers of the 14 top-ranked compounds were submitted to the SC. Telmisartan, terazosin, and ursodeoxycholic acid were selected as the initial interventions.

conclusionsDrug selection in DMT PD MAMS trials requires consideration of scientific and practical issues. We present a robust system that can inform similar initiatives. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Antiparkinson AgentsClinical Trials as TopicParkinson DiseaseHumansAntiparkinson Agentsadaptive clinical trialmethodologyneuroprotectionneuroprotective agentsParkinson's disease

Identifiers

PMID40249275
PMCPMC12273612

What OpenQuestion holds

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LicenceCC BY
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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.