NCT04565665
Study of Cord Blood Derived Mesenchymal Stem Cells for Treatment of Moderate, Severe or Critical Pneumonia
Active, Not Recruiting
PHASE1Ages 18+InterventionalTreatmentM.D. Anderson Cancer CenterInvestigator-initiated
~65 participants
Updated 2026-05-20 on ClinicalTrials.gov
What's tested:Best PracticeMesenchymal Stem Cell
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of composite serious adverse events (Phase I)
Measured over Within 30 days of the first mesenchymal stem cell (MSC) infusion
+3 more outcomes measured
Conditions
Where it's being run
1 sites across 1 statesTexas1
Study leadership
- Amanda Olson · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Exclusion
Moribund participants not expected to survive up to 48 hours
Participants with severe chronic liver disease (Childs-Pugh score \> 10)
Pregnant and/or lactating women
Participants on extracorporeal membrane oxygenation
What this trial measures
- Incidence of composite serious adverse events (Phase I)Within 30 days of the first mesenchymal stem cell (MSC) infusion
Serious adverse events with be comprised of grade 3 or 4 graft versus host disease or death and will be estimated and reported overall and by group, along with 95% confidence intervals.
- Patients alive without grade 3, 4 infusional toxicity (Phase II)At day 30 post MSC infusion
- Patients alive with grade 3 or 4 infusional toxicity (Phase II)At day 30 post MSC infusion
- Patients not alive (Phase II)At day 30 post MSC infusion