Autoantibody Reduction Therapy in Patients With Idiopathic Pulmonary Fibrosis

PHASE2CompletedINTERVENTIONAL
Enrollment

58

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

January 31, 2019

Study Completion Date

November 30, 2020

Conditions
Ambulatory IPF
Interventions
DRUG

Rituximab

i.v. rituximab given on two occasions 14 days apart.

DRUG

Placebo

Subjects randomized to placebo will receive two i.v. doses of 5% dextrose in water (D5W) in the same schedule as the rituximab subjects. The D5W and rituximab preparations will be indistinguishable.

Trial Locations (7)

15213

University of Pittsburgh Medical Center, Pittsburgh

17822

Geisinger Medical Center, Danville

19122

Temple University, Philadelphia

29425

Medical University of South Carolina, Charleston

35233

University of Alabama at Birmingham, Birmingham

55455

University of Minnestoa, Minneapolis

02115

Brigham and Women's Hospital, Boston

All Listed Sponsors
collaborator

National Institutes of Health (NIH)

NIH

lead

University of Alabama at Birmingham

OTHER

NCT01969409 - Autoantibody Reduction Therapy in Patients With Idiopathic Pulmonary Fibrosis | Biotech Hunter | Biotech Hunter