drugset / Trial / NCT01262001

Safety, Tolerability, and Efficacy Study of Idiopathic Pulmonary Fibrosis

NCT01262001

Phase 2 Completed 90 enrolled Kyntra Bio
Non-randomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the safety and tolerability of FG-3019 in subjects with Idiopathic Pulmonary Fibrosis (IPF) and the efficacy of FG-3019 for attenuating fibrosis in these subjects.

Timeline

Start
2011-03
Primary completion
2014-06-26
Completion
2017-06-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Pamrevlumab Monoclonal antibody 15 mg/kg Intravenous
Subject Pamrevlumab Monoclonal antibody 30 mg/kg Intravenous