Status:

COMPLETED

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

Lead Sponsor:

McMaster University

Conditions:

Chronic Obstructive Pulmonary Diseases

Chronic Airways Limitation

Eligibility:

All Genders

40-80 years

Phase:

PHASE3

Brief Summary

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 episo...

Detailed Description

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 a...

Eligibility Criteria

Inclusion

  • 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

  • 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

Key Trial Info

Start Date :

January 1 2012

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2015

Estimated Enrollment :

18 Patients enrolled

Trial Details

Trial ID

NCT01463644

Start Date

January 1 2012

End Date

September 1 2015

Last Update

September 24 2025

Active Locations (1)

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1

Firestone Institute of Respiratory Health, St Joseph's Hospital

Hamilton, Ontario, Canada, L8N 4A6