Safety, Tolerability, and Efficacy Study of Idiopathic Pulmonary Fibrosis

PHASE2CompletedINTERVENTIONAL
Enrollment

90

Participants

Timeline

Start Date

March 31, 2011

Primary Completion Date

June 26, 2014

Study Completion Date

June 21, 2017

Conditions
Idiopathic Pulmonary Fibrosis
Interventions
DRUG

FG-3019

Cohort 1 and Cohort 1-EX: 15 mg/kg by infusion every 3 weeks for 45 weeks in the target population (first treatment year and first extended treatment year and every 3 weeks thereafter for three additional extended treatment years).

DRUG

FG-3019

Cohort 2 and Cohort 2-EX: 30 mg/kg by infusion every 3 weeks for 45 weeks in the target population (first treatment year and first extended treatment year and every 3 weeks thereafter for three additional extended treatment years).

Trial Locations (18)

10029

Mount Sinai, New York

22042

Inova Fairfax Hospital, Falls Church

30322

Emory University, Atlanta

32803

Central Florida Pulmonary Group, PA, Orlando

33606

Tampa General Hospital, Tampa

35294

University of Alabama at Birmingham Hospital, Birmingham

37232

Vanderbilt University, Nashville

40202

University of Louisville, Louisville

43221

The Ohio State University, Columbus

53705

University of Wisconsin School of Medicine & Public Health, Madison

63017

St. Luke's Hospital, Chesterfield

67208

Via Christi Hospitals Wichita, Inc., Wichita

75390

University of Texas Southwestern Medical Center, Dallas

84108

University of Utah - Lung Health Research, Salt Lake City

85258

Arizona Pulmonary Specialists, LTD, Scottsdale

06520

Yale University, New Haven

08901

Rutgers-Robert Wood Johnson Medical School, New Brunswick

05446

Vermont Lung Center, Colchester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

FibroGen

INDUSTRY