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Clinical trial

A Phase I Open-Label, Dose-Escalation Study to Evaluate Safety, Tolerability, and Efficacy of Allogeneic Placenta-derived Human Mesenchymal Stem Cells for the Treatment of Acute Respiratory Distress Syndrome

NCT05886985 is registered in ClinicalTrials.gov with BioSpring Medical Co., Ltd as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase I Open-Label, Dose-Escalation Study to Evaluate Safety, Tolerability, and Efficacy of Allogeneic Placenta-derived Human Mesenchymal Stem Cells for the Treatment of Acute Respiratory Distress Syndrome
Lead sponsor
BioSpring Medical Co., Ltd
Phase
Phase 1
Overall status
Not yet recruiting
Start date
December 31, 2023
Completion date
May 31, 2027
Enrollment
24 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

acute respiratory distress syndrome