drugset / Trial / NCT01759511

Long-Term Safety Study of GS-6624 in Adults With Idiopathic Pulmonary Fibrosis (IPF)

NCT01759511

Phase 2 Terminated 34 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the long term safety and tolerability of simtuzumab (GS-6624) in participants with idiopathic pulmonary fibrosis (IPF) who had previously participated in Gilead clinical trial AB0024-201.

Timeline

Start
2012-10-18
Primary completion
2016-02-19
Completion
2016-02-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Simtuzumab Monoclonal antibody 125 mg/ml Intravenous
Subject Simtuzumab Monoclonal antibody 200 mg/ml Intravenous