drugset / Trial / NCT00143611
Efficacy & Safety of Resatorvid in Adults With Severe Sepsis
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to determine the optimal dose of Resatorvid for reducing 28-day all-cause mortality in subjects with severe sepsis.
Timeline
- Start
- 2005-09
- Primary completion
- 2007-02
- Completion
- 2007-02
Outcome
Missed primary endpoint
paper 17% in the high-dose group (p = .26 for placebo vs. high dose). PMID 20562702 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Resatorvid | Small molecule | 1.2 mg/kg | Subcutaneous |
| Subject | Resatorvid | Small molecule | 2.4 mg/kg | Subcutaneous |