drugset / Trial / NCT02104713

Stem Cell Therapy to Improve Burn Wound Healing

NCT02104713 ↗

NaSingle-groupOpen-labelHealth-services research

Summary

This study will determine the safety of allogeneic stem cell therapy from healthy donors, for 2nd degree burn wounds of less than 20% Total Body Surface Area (TBSA), at four different dose levels. Clinical evaluation will take place every 1 to 4 weeks intervals until wound closure, and then monthly for 6 months following the last administration of MSCs. Once the safety and dose-response analysis in Phase 1 is completed, an expanded trial will be initiated to better examine the efficacy of MSC therapy in 2nd degree burn wounds. Phase 1 will establish the maximum safe dose that will be used in the Phase II trial.

Timeline

Start
2014-06-04
Primary completion
2019-03-18
Completion
2019-03-18

Drugs

EvaluationDrugModalityDoseRoute
Subject mesenchymal stem cells Cell therapy 2500 cells —
Subject mesenchymal stem cells Cell therapy 5000 cells —
Subject mesenchymal stem cells Cell therapy 10000 cells —
Subject mesenchymal stem cells Cell therapy 20000 cells —

Indications

No indication recorded.