Prostaglandin Inhibition for Emphysema
NCT02006576 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 118
Last updated 2023-12-13
Summary
The Prostaglandin Inhibition for Emphysema (PIE) study will determine if a currently available therapy, ibuprofen 600 mg three times daily, can block PGE production in the lower respiratory tract and if this results in improvement in measures of lung repair function.
Conditions
- Emphysema
Interventions
- DRUG
-
600 mg ibuprofen three times daily for 48 weeks
- OTHER
-
Placebo three times daily
Sponsors & Collaborators
-
National Jewish Health
collaborator OTHER -
Temple University
collaborator OTHER -
University of California, Los Angeles
collaborator OTHER -
University of Alabama at Birmingham
collaborator OTHER -
University of Nebraska
lead OTHER
Principal Investigators
-
Stephen I Rennard, MD · University of Nebraska
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 46 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2014-01-01
- Primary Completion
- 2018-03-31
- Completion
- 2018-03-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Efficacy and Safety of Alpha1-Proteinase Inhibitor (Human), Modified Process (Alpha-1 MP) in Subjects With Pulmonary Emphysema Due to Alpha1 Antitrypsin Deficiency (AATD)
NCT01983241 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Phase 2 Study to Evaluate the Safety and Tolerability of PBI-4050 in Patients With Idiopathic Pulmonary Fibrosis (IPF)
NCT02538536 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Pharmacodynamics, and Pharmacokinetics of Orally Administered BLD-2660 in Subjects With IPF
NCT04244825 ·Status: WITHDRAWN ·Phase: PHASE2
-
Efficacy/Safety of HA Inhalation Solution for Hereditary Emphysema in Patients With Alpha-1 Antitrypsin Deficiency
NCT03114020 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), Pharmacodynamics (PD) and Food Effect of Single or Repeat Doses of GSK2793660 in Healthy Subjects
NCT02058407 ·Status: TERMINATED ·Phase: PHASE1
-
Inhaled Treprostinil for Dyspnea and Exercise Intolerance in Mild COPD
NCT06969573 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Efficacy and Safety of Nintedanib in Patients With Progressive Fibrosing Interstitial Lung Disease (PF-ILD)
NCT02999178 ·Status: COMPLETED ·Phase: PHASE3
-
Single Doses of GSK3008348 in Idiopathic Pulmonary Fibrosis (IPF) Participants Using Positron Emission Tomography (PET) Imaging
NCT03069989 ·Status: TERMINATED ·Phase: PHASE1
-
Safety and Efficacy of a Lysophosphatidic Acid Receptor Antagonist in Idiopathic Pulmonary Fibrosis
NCT01766817 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy of Pirfenidone in Patients With Idiopathic Pulmonary Fibrosis
NCT00287729 ·Status: COMPLETED ·Phase: PHASE3
-
A Study in Patients With Non-cystic Fibrosis Bronchiectasis to Test How Well Different Doses of BI 1323495 Are Tolerated and How BI 1323495 Affects Biomarkers of Inflammation
NCT04656275 ·Status: TERMINATED ·Phase: PHASE1
-
Three-Arm Study of the Safety and Efficacy of Pirfenidone in Patients With Idiopathic Pulmonary Fibrosis
NCT00287716 ·Status: COMPLETED ·Phase: PHASE3
-
To Evaluate the Effect of Different Doses of SAR156597 Given to Patients With Idiopathic Pulmonary Fibrosis (IPF)
NCT01529853 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Study of Efficacy and Safety of Inhaled Treprostinil in Subjects With Idiopathic Pulmonary Fibrosis
NCT04708782 ·Status: COMPLETED ·Phase: PHASE3
-
Phase 1, Safety and Bronchopulmonary PK Study in Healthy Volunteers
NCT03691584 ·Status: COMPLETED ·Phase: PHASE1
-
A Study Measuring the Effectiveness, Safety, and Tolerability of BMS-986278 in Participants With Lung Fibrosis
NCT04308681 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Single and Repeat Doses of the Dry Powder Formulation of GSK2269557 in Healthy Subjects
NCT01762878 ·Status: COMPLETED ·Phase: PHASE1
-
Effect of a Component of Fish Oil on Exercise-Induced Bronchoconstriction and Airway Inflammation in Asthma
NCT01504646 ·Status: COMPLETED ·Phase: NA
-
Study of Pharmacodynamics, Pharmacokinetics, Safety and Tolerability of VAY736 in Patients With Idiopathic Pulmonary Fibrosis
NCT03287414 ·Status: TERMINATED ·Phase: PHASE2
-
Safety, Tolerability and PK of Nintedanib in Combination With Pirfenidone in IPF
NCT02579603 ·Status: COMPLETED ·Phase: PHASE4
-
TD-1058 First-In-Human Study in Healthy Subjects and Subjects With Idiopathic Pulmonary Fibrosis
NCT04589260 ·Status: TERMINATED ·Phase: PHASE1
-
A Study to Test How Taking BI 1015550 for 12 Weeks Affects Lung Function in People With Idiopathic Pulmonary Fibrosis (IPF)
NCT04419506 ·Status: COMPLETED ·Phase: PHASE2
-
Tiotropium Bromide Inhalation Solution in Subjects With Chronic Obstructive Pulmonary Disease
NCT04780984 ·Status: COMPLETED ·Phase: PHASE2
-
Study of the Efficacy and Safety of Inhaled Treprostinil in Subjects With Progressive Pulmonary Fibrosis (TETON-PPF)
NCT05943535 ·Status: RECRUITING ·Phase: PHASE3
-
Expanded Access Program of Nintedanib in Patients With Idiopathic Pulmonary Fibrosis (EAP)
NCT02171156 ·Status: APPROVED_FOR_MARKETING