Skip to main content
OpenTrials
Completed

NCT Number: NCT01463644

Mepolizumab in Chronic Obstructive Pulmonary Diseases (COPD) With Eosinophilic Bronchitis

Some patients with chronic obstructive pulmonary diseases (COPD) have large number of specific white blood cells called eosinophils in their airways. These cells are also responsible for causing episodes of worsened respiratory symptoms (exacerbations) and often cause irreversible damage to the airways . This subset of COPD patients often require oral steroids to bring down the number of eosinophils in their airways. Steroids have harmful effects on several of our body systems like bones, blood pressure, blood glucose control and can cause recurrent infections. Mepolizumab is a drug that specifically targets eosinophils reducing the number in the airway. This drug has been shown to be effective in decreasing exacerbation rates and time to exacerbation in asthma patients with eosinophils in their airways. Targeting eosinophils in COPD patients has been shown to reduce severe exacerbations. Hence it is likely that COPD patients with eosinophils in their airways will benefit similarly and have reduced rates and time to exacerbation.

Study Hypothesis:Does mepolizumab decrease sputum eosinophils in patients with fixed airflow obstruction (COPD) and eosinophilic bronchitis?

Completed

Looking for future studies?

Notify Me

Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Firestone Institute of Respiratory Health, St Joseph's Hospital

Hamilton, Ontario, L8N 4A6, Canada

About this study

It is thus likely that a specific treatment such as anti-IL5 directed against eosinophils would be superior to the current standard treatment in decreasing sputum eosinophil counts and exacerbations and decrease structural changes (remodelling) in patients with COPD who continue to have eosinophils in their airway and whose airway disease has an eosinophil-driven component as evidenced by persistent airway eosinophilia.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis: An established clinical history of COPD in accordance with the definition by the American Thoracic Society/European Respiratory Society as follows: Chronic obstructive pulmonary disease is a preventable and treatable disease state characterized by airflow limitation that is not fully reversible. The airflow limitation is usually progressive and is associated with an abnormal inflammatory response of the lungs to noxious particles or gases, primarily caused by cigarette smoking. Although COPD affects the lungs, it also produces significant systemic consequences
  • Sputum eosinophils > 3% at randomization and on at least one occasion in the past 2 years. If this historic data is not available, documented improvement in Forced expired volume in 1 second (FEV1) of at least 12% with a course of prednisone in the past 2 years will be used as a surrogate for the presence of airway eosinophilia
  • FEV1/Vital Capacity (VC) < 70% and FEV1 < 60% of predicted normal values calculated using NHANES III reference equations at Screening Visit
  • At least one major exacerbation requiring prednisone in the preceding 12 months. If patients are currently well controlled by optimizing their sputum cell counts (eosinophils < 2%), they should have documented history of exacerbations when their eosinophilia was uncontrolled.
  • A signed and dated written informed consent prior to study participation.
  • Smoking History: Current or former cigarette smokers with a history of cigarette smoking of greater than 10 pack-years [number of pack years = (number of cigarettes per day/20) x number of years smoked (e.g., 20 cigarettes per day for 10 years, or 10 cigarettes per day for 20 years]. Former smokers are defined as those who have stopped smoking for at least 6 months prior to Screening Visit
  • Male or female adults. A female is eligible to enter and participate in the study if she is either of Non-child bearing potential or is of child bearing age and has a negative pregnancy test at screening, and agrees to acceptable contraceptive methods used consistently and correctly

Exclusion criteria

  • Current asthma (12% reversibility to a bronchodilator)
  • Sputum eosinophils < 3% on fluticasone (or equivalent) of 250µg bid.
  • Inability to use salmeterol or tiotropium
  • Significant co-morbidity that prevents from participating in the study
  • Known bronchiectasis or immune deficiency disorders that would predispose the patients to recurrent infections.
  • Pregnancy or intent to become pregnant and lactating females
  • Drug or Alcohol Abuse: A known or suspected history of alcohol or drug abuse within 2 years prior to Screening Visit

Treatment and study plan

Mepolizumab

Drug

This is an anti IL-5 which is given once a month intravenously at the dose of 750 mg.

Other names: SB-240563

Placebo

Drug

The placebo will consist of 100 mL normal saline solution (0.9%, 154 mmol/L sodium chloride).

Other names: Normal saline

Primary outcomes

  1. Percentage Decrease of Sputum Eosinophils From Baseline to End of Therapy (6 Months)

    Time frame: 6 months

    The results will be expressed as absolute changes in percent sputum eosinophil counts from baseline to end of therapy (at 6 months).

    Change is difference in sputum eosinophils between baseline/time zero to end of therapy/6 months.

    A larger number represents a greater degree in the reduction of sputum eosinophils.

Secondary outcomes

  1. Proportion of Patients With a Major Exacerbation.

    Time frame: Baseline to 6 months

    Exacerbation: a sustained worsening of the patient's respiratory condition, from the stable state and beyond normal day-to-day variations, necessitating a change in regular medication in a patient with underlying COPD Major exacerbation will be defined as a symptomatic deterioration requiring treatment with antibiotics, oral or intravenous corticosteroids, hospitalization, or a combination of these.

Sponsors and collaborators

Lead sponsor

McMaster University

Other

Registry information

Official study title

Mepolizumab in COPD With Eosinophilic Bronchitis: A Randomized Clinical Trial

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Nov 2, 2011
Registry last updated
Sep 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.