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