ArticleCell reports. Medicine2026
Intravenous human umbilical cord-derived mesenchymal stem cell transplantation for ischemic stroke (MERIT): A phase 1 trial.
Article in Cell reports. Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05697718 (A Phase I Study of Safety and Tolerability of Single-dose Human Umbilical Cord Mesenchymal Stem Cell), which is not on this map. Cited by 1 paper.
What it found
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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.
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.
A Phase I Study of Safety and Tolerability of Single-dose Human Umbilical Cord Mesenchymal Stem Cell (IxCell hUC-MSC-S) in Patients With Convalescent Phase of Ischemic Stroke
Who cites it
1 citing paper in PubMed.
- Stem cell and stem cell-derived extracellular vesicle therapy for traumatic brain injury: mechanisms, engineering and translation.Frontiers in neuroscience · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
21 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Umbilical cord-derived mesenchymal stem cells (UC-MSCs) hold promise as a potential therapy for ischemic stroke, but the optimal transplantation strategy remains to be explored. This open-label, single-arm, phase 1 study enrolls 18 patients with subacute ischemic stroke and National Institutes of Health Stroke Scale (NIHSS) scores of 6-20 (median, 9; interquartile range, 8-12). The patients receive a single intravenous transplantation of 50, 100, or 200 million UC-MSCs (n = 6 for each dose) and are followed for 24 weeks. The primary outcome is safety and tolerability, with secondary assessment of preliminary efficacy and exploratory analyses of immunological changes. Possible treatment-related adverse events include dizziness, nausea, sweating, fatigue, and epilepsy. No serious adverse event occurs. A reduction in NIHSS score by 1-5 points is observed in 14 patients during follow-up. In conclusion, intravenous administration of UC-MSCs is well-tolerated in subacute ischemic stroke. The trial is registered on ClinicalTrials.gov (NCT05697718).
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Registered trials
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