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Regenerative stem cell therapy for stroke in Europe (RESSTORE): a multicenter randomized controlled efficacy clinical trial

Authors :
Loïc Legris
Anaick Moisan
Assia Jaillard
Louise Bonnet
Thierry Moulin
Igor Sibon
Emmanuel Touzé
Isabelle Favre-Wiki
Charlotte Cordonnier
Lucie Dellaschiava
Mikael Mazighi
Charlotte Rosso
Sonia Alamowitch
David Calvet
Marianne Barbieux-Guillot
Stephan Roux
Alain-Ali Mojallal
Fabien Boucher
Antoine Thuriot
Julie Soulard
Bernadette Naegele
Dominic Perennou
Matthieu Roustit
Zaza Putkaradze
Marc Hommel
Audrey Lehmann
Julien Colombat
Fatima Chorfa
Delphine Maucort-Boulch
Laurent Lamalle
Sylvie Grand
Alexandre Krainik
Olivier Detante
Source :
Frontiers in Stroke, Vol 3 (2024)
Publication Year :
2024
Publisher :
Frontiers Media S.A., 2024.

Abstract

IntroductionEncouraging the activation of brain repair mechanisms and fostering spontaneous functional recovery in stroke patients hold great promise for alleviating the global burden of this condition and allowing an extended therapeutic time window. Cell-based regenerative therapy (with mesenchymal stem/stromal cells, such as adipose-derived stem cells [ADSCs]) is particularly attractive considering its excellent safety profile, low immunogenicity after allogeneic application, and well-established functional benefits on stroke recovery in animal models. This study aims to assess the efficacy and safety effects of intravenous (IV) infusion of freshly cultured allogeneic ADSCs on recovery after ischemic stroke.Population and methodsRESSTORE is a multicentric, randomized 1:1 controlled double-blind clinical trial. Eighty patients will be enrolled in nine French stroke centers. The main inclusion criteria are ≥18 years of age, acute hemispheric ischemic stroke, and a National Institutes of Health Stroke Scale (NIHSS) score of ≥7, including a motor subscore of ≥3. According to the previous dose-escalation safety trial data, the maximum tolerated dose of 3 million ADSCs/kg was selected. IV infusion was performed within 10 days following stroke onset, with a follow-up over 2 years.OutcomesThe primary endpoint is the motor NIHSS subscore, computed as the sum of the upper limb, lower limb, and hand scores, measured 6 months after stroke onset to assess motor recovery. The secondary outcomes are the occurrence of death/serious adverse events, clinical scores (the detailed NIHSS scores, Montreal Cognitive Assessment scores, modified Rankin Scale scores, Aphasia Handicap Scores, Depression Intensity Scale Circles scores, Fatigue Scale scores, etc.), immune monitoring (for the first 30 patients), and multimodal biomarkers derived from diffusion and functional magnetic resonance imaging.DiscussionThis study may provide some evidence for the effects of freshly cultured allogenic ADSCs IV infusion in subacute stroke that may help design a larger international randomized controlled trial.

Details

Language :
English
ISSN :
28133056
Volume :
3
Database :
Directory of Open Access Journals
Journal :
Frontiers in Stroke
Publication Type :
Academic Journal
Accession number :
edsdoj.88f02ae2bed74302aa4ed8ed9d9281d4
Document Type :
article
Full Text :
https://doi.org/10.3389/fstro.2024.1416490