drugset / Trial / NCT02104713
Stem Cell Therapy to Improve Burn Wound Healing
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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.