Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07413978Phase 2Recruiting
Phase 2, open-label trial of human umbilical cord mesenchymal stem cells in acute respiratory distress syndrome (ARDS), sponsored by Changchun Tuohua Pharmaceutical. Primary endpoints: Dose Limiting Toxicity incidence rate at 28 days, Maximum Tolerated Dose and 1 more. Started Apr 2025; status: recruiting.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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