drugset / Trial / NCT01629667

A Phase 2, Randomized Dose-ranging Study to Evaluate the Efficacy of Tralokinumab in Adults With Idiopathic Pulmonary Fibrosis

NCT01629667

Phase 2 Terminated 409 enrolled MedImmune LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

To study the safety and effectiveness of multiple-doses of tralokinumab on pulmonary function in adults with mild to moderate idiopathic pulmonary fibrosis (IPF). IPF is a chronic, progressive, irreversible, and usually fatal lung disease of unknown cause.

Timeline

Start
2012-10
Primary completion
2015-05
Completion
2016-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Tralokinumab Monoclonal antibody 400 mg Intravenous
Subject Tralokinumab Monoclonal antibody 800 mg Intravenous