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.