drugset / Trial / NCT00996840

SB-681323 IV for Subjects at Risk of Acute Lung Injury or ARDS

NCT00996840

Phase 2 Completed 77 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindTreatment

Summary

This is an early phase (Phase IIa), randomized, double-blind, parallel group, multi-centre study for subjects with trauma (physical injury) who are at risk for developing Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS). The primary purpose of the study is to evaluate the safety and tolerability of SB-681323, which is a potent, selective inhibitor of p38 alpha (MAPK) (prevents inflammation of tissue), in comparison to a placebo.

Timeline

Start
2009-10-16
Primary completion
2013-02-09
Completion
2013-02-09

Drugs

EvaluationDrugModalityDoseRoute
Subject dilmapimod Small molecule 3 mg Intravenous
Subject dilmapimod Small molecule 7.5 mg Intravenous
Subject dilmapimod Small molecule 10 mg Intravenous

Indications