34
Participants
Start Date
October 18, 2012
Primary Completion Date
February 19, 2016
Study Completion Date
February 19, 2016
Simtuzumab
200 mg/mL administered intravenously biweekly (per original protocol) or 125 mg/mL self-administered subcutaneously every 7 ± 2 days (per protocol amendment 1)
University of Pittsburgh Medical Center, Pittsburgh
Medical University of South Carolina, Charleston
Vanderbilt University Medical Center, Nashville
Arizona Pulmonary Specialists, Ltd., Scottsdale
University of California, Los Angeles
Stanford University Medical Center, Stanford
Lead Sponsor
Gilead Sciences
INDUSTRY