drugset / Trial / NCT06505941

Clinical Study on the Safety and Preliminary Efficacy of hUC-MSCs Intravenous Infusion Therapy for ARDS

NCT06505941

RandomizedParallel-groupDouble-blindTreatment

Summary

The object of this study is to observe the safety of umbilical cord mesenchymal stem cell therapy for acute respiratory distress syndrome, consisting with two phases.

Timeline

Start
2024-07-20
Primary completion
2025-11-20
Completion
2027-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Umbilical Cord Mesenchymal Stem Cell Cell therapy 1e+06 cells/kg Intravenous
Subject Umbilical Cord Mesenchymal Stem Cell Cell therapy 5e+06 cells/kg Intravenous
Subject Umbilical Cord Mesenchymal Stem Cell Cell therapy 1e+07 cells/kg Intravenous