drugset / Trial / NCT01597635
The Safety, Tolerability, PK and PD of GSK2586881 in Patients With Acute Lung Injury
RandomizedParallel-groupTriple-blindTreatment
Summary
This is an early phase (phase IIa), randomized, multi-center study in subjects with acute lung injury (ALI) or acute respiratory distress syndrome (ARDS). The purpose of this study is to investigate the safety of GSK2586881 and to determine what effects it has on people with Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS). The study has two parts: Part A will be an open-label investigation in five subjects. Part B will be a double-blind, placebo controlled investigation and will involve approximately 60 subjects.
Timeline
- Start
- 2012-09-01
- Primary completion
- 2014-10-01
- Completion
- 2014-10-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GSK2586881 | Protein / enzyme biologic | 0.1 mg/kg | Intravenous |
| Subject | GSK2586881 | Protein / enzyme biologic | 0.4 mg/kg | Intravenous |
| Subject | GSK2586881 | Protein / enzyme biologic | 0.8 mg/kg | Intravenous |