Stopped: Study was suspended pending renovation and reopening of the facility manufacturing the study product, and the study was ultimately terminated in February of 2026.
The protocol is a phase I open label study evaluating the safety and feasibility of peri-transplant infusion of freshly expanded interferon gamma primed MSCs in adult and pediatric patients undergoing HCT for acute leukemia and myelodysplastic syndrome (MDS).
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Number of successful preparations and deliveries of investigational product
Timeframe: Day 1 (day of infusion)
Number of adverse events attributed to the investigational product
Timeframe: Day 2 (day after infusion)
Maximal Tolerated Dose
Timeframe: Day 2 (day after infusion)