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Zileuton for the Treatment of Idiopathic Pulmonary Fibrosis

Primary Purpose

Idiopathic Pulmonary Fibrosis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
zileuton
azathioprine/prednisone
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Pulmonary Fibrosis

Eligibility Criteria

35 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of idiopathic pulmonary fibrosis Taking < 15 mg prednisone for at least 30 days prior to screening Age 35-80, inclusive Able to understand a written informed consent and comply with the study protocol Exclusion Criteria: Significant environmental exposure Diagnosis of collagen vascular disease Evidence of active infection Clinically significant cardiac disease Myocardial infarction, coronary artery bypass or angioplasty within 6mo Unstable angina pectoris Congestive heart failure requiring hospitalization within 6 months Uncontrolled arrhythmia Poorly controlled or severe diabetes mellitus Pregnancy or lactation Women of childbearing potential not using a medically approved means of contraception (i.e. oral contraceptives, intrauterine devices, diaphragm, Norplant) Current enrollment in another experimental protocol Physiologic Criteria: FEV1/FVC < 0.60 Laboratory Criteria: Total bilirubin > 1.5 X upper limit normal AST or ALT > 3X upper limit normal Alkaline phosphatase > 3X upper limit normal White blood cell count < 2,500/mm3 Hematocrit < 30% Platelets < 100,000/mm3 Prothrombin time INR > 1.5

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

zileuton

azathioprine/prednisone

Arm Description

Zileuton

azathioprine/prednisone

Outcomes

Primary Outcome Measures

LTB4 level in BAL

Secondary Outcome Measures

CRP score

Full Information

First Posted
September 12, 2005
Last Updated
December 2, 2015
Sponsor
University of Michigan
Collaborators
National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00262405
Brief Title
Zileuton for the Treatment of Idiopathic Pulmonary Fibrosis
Official Title
Phase II Trial of Zileuton Compared to Azathioprine/Prednisone for the Treatment of Idiopathic Pulmonary Fibrosis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
January 2001 (undefined)
Primary Completion Date
May 2007 (Actual)
Study Completion Date
May 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Institutes of Health (NIH)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Open label trial of zileuton compared to azathioprine/prednisone for patients with idiopathic pulmonary fibrosis. Study subjects will undergo a detailed clinical, radiographic, and physiologic assessment at baseline. Subjects will be monitored off treatment for three months for changes in symptoms and physiology. Subjects will then be randomized to six months of treatment with zileuton or azathioprine/prednisone. The primary endpoint of this trial is change in LTB4 levels in bronchoalveolar lavage fluid following six months of treatment. Secondary endpoints are progression free survival, change in dyspnea, change in quality of life, and change in physiology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Pulmonary Fibrosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
zileuton
Arm Type
Experimental
Arm Description
Zileuton
Arm Title
azathioprine/prednisone
Arm Type
Active Comparator
Arm Description
azathioprine/prednisone
Intervention Type
Drug
Intervention Name(s)
zileuton
Intervention Type
Drug
Intervention Name(s)
azathioprine/prednisone
Primary Outcome Measure Information:
Title
LTB4 level in BAL
Time Frame
6 months
Secondary Outcome Measure Information:
Title
CRP score
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of idiopathic pulmonary fibrosis Taking < 15 mg prednisone for at least 30 days prior to screening Age 35-80, inclusive Able to understand a written informed consent and comply with the study protocol Exclusion Criteria: Significant environmental exposure Diagnosis of collagen vascular disease Evidence of active infection Clinically significant cardiac disease Myocardial infarction, coronary artery bypass or angioplasty within 6mo Unstable angina pectoris Congestive heart failure requiring hospitalization within 6 months Uncontrolled arrhythmia Poorly controlled or severe diabetes mellitus Pregnancy or lactation Women of childbearing potential not using a medically approved means of contraception (i.e. oral contraceptives, intrauterine devices, diaphragm, Norplant) Current enrollment in another experimental protocol Physiologic Criteria: FEV1/FVC < 0.60 Laboratory Criteria: Total bilirubin > 1.5 X upper limit normal AST or ALT > 3X upper limit normal Alkaline phosphatase > 3X upper limit normal White blood cell count < 2,500/mm3 Hematocrit < 30% Platelets < 100,000/mm3 Prothrombin time INR > 1.5
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Galen B Toews, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Zileuton for the Treatment of Idiopathic Pulmonary Fibrosis

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