drugset / Trial / NCT01371305

STX-100 in Patients With Idiopathic Pulmonary Fibrosis (IPF)

NCT01371305 ↗

Phase 2 Completed 41 enrolled Biogen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of subcutaneously (SC) administered multiple, escalating doses of BG00011 (a humanized monoclonal antibody directed against the alpha v beta 6 (αvβ6) integrin, formerly known as STX-100) in participants with IPF. The Secondary objectives are to estimate the pharmacokinetic (PK) parameters after the 1st dose and after the last dose of multiple, escalating doses of BG00011 in participants with IPF, to assess the immunogenicity of BG00011 in participants with IPF, and to assess the effect of BG00011 on biomarkers isolated from bronchoalveolar lavage (BAL) and peripheral blood in participants with IPF.

Timeline

Start
2012-07-16
Primary completion
2017-03-31
Completion
2017-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BG00011 Monoclonal antibody — Subcutaneous