drugset / Trial / NCT00143611

Efficacy & Safety of Resatorvid in Adults With Severe Sepsis

NCT00143611

Phase 3 Completed 277 enrolled Takeda
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

Drugs

EvaluationDrugModalityDoseRoute
Subject Resatorvid Small molecule 1.2 mg/kg Subcutaneous
Subject Resatorvid Small molecule 2.4 mg/kg Subcutaneous