drugset / Trial / NCT00886470
ST266 Versus Standard Care In Treating Partial Thickness Burns
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The objective of this protocol is to perform a safety and dose-determination efficacy clinical trial in patients having a degree of partial-thickness burn wounds. The trial will be a prospectively randomized and double-blind trial of ST266 compared with standardized care using 0.9% NaCl (normal saline) solution in the same three treatment regimens.
Timeline
- Start
- 2009-06
- Primary completion
- 2010-03
- Completion
- 2010-03
Outcome
Outcome not reported
Stopped (Enrollment): “This study was terminated early due to slow accrual of patients.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ST266 | Protein / enzyme biologic | 0.01 unknown | Topical |
Indications
No indication recorded.