We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov Menu

Autoantibody Reduction Therapy in Patients With Idiopathic Pulmonary Fibrosis (ART-IPF)

This study is currently recruiting participants.
Verified November 2016 by University of Alabama at Birmingham
ClinicalTrials.gov Identifier:
First Posted: October 25, 2013
Last Update Posted: December 9, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
National Institutes of Health (NIH)
Information provided by (Responsible Party):
University of Alabama at Birmingham

Recent research studies have suggested that proteins called antibodies that are produced by the immune system might be involved in the lung damage of idiopathic pulmonary fibrosis (IPF). Antibodies produced by the immune system normal help to fight infections by attacking bacteria and viruses without harming our own tissues. In patients with IPF, there is evidence that certain antibodies (called autoantibodies) attack the lung and contributes to the injury and scarring that occurs in IPF. Our recent studies have found that many IPF patients appear to have excessive autoantibody levels in blood and lungs that might make their disease worse.

Rituximab is a medication approved by the Food and Drug Administration (FDA) for the treatment of autoantibody diseases such as rheumatoid arthritis. Rituximab works by destroying B cells, a type of white blood cell, called a B-lymphocyte, which produce autoantibodies. In this research study, rituximab will be given into a vein to reduce the autoantibody levels that we believe might be contributing to the lung damage in IPF.

This study is being conducted to determine if rituximab provides beneficial effects for IPF patients by decreasing further lung injury.

Condition Intervention Phase
Ambulatory IPF Drug: Rituximab Drug: Placebo Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
Official Title: Autoantibody Reduction Therapy in Patients With Idiopathic Pulmonary Fibrosis (ART-IPF)

Resource links provided by NLM:

Further study details as provided by University of Alabama at Birmingham:

Primary Outcome Measures:
  • Autoantibodies to HEp-2 Cells [ Time Frame: 9 months ]
    Titers of anti-HEp-2 autoantibodies, by indirect immunofluorescence assays (IFA) over 9 months

Secondary Outcome Measures:
  • Anti-Heat Shock Protein 70 (HSP70) autoantibodies [ Time Frame: 9 months ]
    Changes of anti-HSP70 plasma concentrations as determined by ELISA

  • Forced Vital Capacity (FVC) as a percentage of predicted values (FVC%p) [ Time Frame: 9 months ]
    Serial FVC%p values over the observation period will be measured by spirometry.

  • Adverse Event (AE) Rates [ Time Frame: 9 months ]
    AE in the two treatment arms will be compared.

  • Acute exacerbation frequency [ Time Frame: 9 months ]
    The number and frequency of acute exacerbations, defined using consensus criteria (new/worsened hypoxemia and dyspnea, with characteristic radiographic changes within the last 30 days).

  • Survival [ Time Frame: 9 months ]
    Absolute and transplant-free survival in the two arms.

  • Hospitalization rates [ Time Frame: 9 months ]
    The frequency and duration of hospitalizations in the two arms will be compared.

Estimated Enrollment: 58
Study Start Date: January 2014
Estimated Study Completion Date: October 2018
Estimated Primary Completion Date: October 2018 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Placebo Comparator: Placebo
These subjects will receive i.v. placebo (5% dextrose in water) administered identically to the rituximab.
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.
Other Name: Placebo (D5W) i.v.
Experimental: Rituximab
Rituximab i.v. given on two occasions, with 14 days between doses.
Drug: Rituximab
i.v. rituximab given on two occasions 14 days apart.

Detailed Description:

This is a double-blinded, Phase II trial in which 58 ambulatory IPF patients at any of four medical centers (University of Pittsburgh, University of Chicago, Geisinger Medical Center, and Temple University) will be randomized equally to 1. placebo or 2. two doses of rituximab 1 gm i.v., with a 14 day interval inbetween doses.

Subjects will be followed for 9 months.


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   50 Years to 85 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

Ambulatory patients with a diagnosis of IPF, not established >5 years from the enrollment date, that fulfills ATS/ETS Consensus Criteria.

Ability and willingness to give informed consent. Presence of autoantibodies against HEp-2 cells, the assay for the primary endpoint.

Age 50-85 y.o.

Exclusion Criteria:

Diagnoses of current infection, proven or suspected by participating physicians based upon their clinical assessments.

Presence of active hepatitis B or C, or HIV infection. Presence of positive CONVENTIONAL autoimmune serologic tests, e.g., ANA, RF, Anti-Ro, Anti-LA, Anti-RNP, Anti-Jo-1.

History of reaction to murine-derived products or any of the trial medications, or prior exposures to human-murine chimeric antibodies.

Malignancy, excluding basal or squamous cell skin cancer and low-risk prostate cancer, defined as stage T1 or T2a with PSA less than 10 ng/dl.

Unwillingness to complete post-treatment surveillance for 9 months. Diagnosis of major morbidities (aside from IPF) expected to interfere with subjects' study participation for 9 months.

Treatment for >5 days within the preceding month with >10 mg. prednisone (or equivalent corticosteroid) or any treatment during the preceding month with a potent cellular immunosuppressant (e.g., cyclophosphomide, methotrexate, mycophenolate, azathioprine, calcineurin inhibitors, etc.).

Uncontrolled diabetes or hypertension that preclude safe treatment with methylprednisolone.

Concurrent participation in other experimental trials.

Pregnancy or unwillingness to use contraception during the duration of the study among female participants with child-bearing potential.

Ratio of forced expiratory volume in 1 second to forced vital capacity (FEV1/FVC) <70% of predicted values.

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01969409

Contact: Steven R Duncan, MD duncsr19@uab.edu

United States, Alabama
University of Alabama at Birmingham Recruiting
Birmingham, Alabama, United States, 35233
Contact: Steve Duncan, MD       duncsr19@uab.edu   
University of Alabama at Birmingham Recruiting
Birmingham, Alabama, United States, 35233
Contact: Steven Duncan, MD         
United States, Illinois
University of Chicago Withdrawn
Chicago, Illinois, United States
United States, Massachusetts
Brigham and Women's Hospital Recruiting
Boston, Massachusetts, United States
Contact: Ivan Rosa, MD         
United States, Minnesota
University of Minnestoa Recruiting
Minneapolis, Minnesota, United States
Contact: Hyun Kim, MD         
United States, Pennsylvania
Geisinger Medical Center Not yet recruiting
Danville, Pennsylvania, United States
Temple University Recruiting
Philadelphia, Pennsylvania, United States
University of Pittsburgh Medical Center Recruiting
Pittsburgh, Pennsylvania, United States, 15213
Principal Investigator: Kevin Gibson, MD         
United States, South Carolina
Medical University of South Carolina Not yet recruiting
Charleston, South Carolina, United States
Contact: Tim Whelean, MD         
Sponsors and Collaborators
University of Alabama at Birmingham
National Institutes of Health (NIH)
Principal Investigator: Steven R Duncan, MD University of Alabama at Birmingham
  More Information

Responsible Party: University of Alabama at Birmingham
ClinicalTrials.gov Identifier: NCT01969409     History of Changes
Other Study ID Numbers: HL119960
First Submitted: October 17, 2013
First Posted: October 25, 2013
Last Update Posted: December 9, 2016
Last Verified: November 2016

Keywords provided by University of Alabama at Birmingham:

Additional relevant MeSH terms:
Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
Idiopathic Interstitial Pneumonias
Lung Diseases
Lung Diseases, Interstitial
Pathologic Processes
Respiratory Tract Diseases
Antineoplastic Agents
Immunologic Factors
Physiological Effects of Drugs
Antirheumatic Agents