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Phase 3 N=238 Randomized Double-blind Treatment

Mepolizumab for COPD Hospital Eosinophilic Admissions Pragmatic Trial

COPD · Eosinophilia

Enrolled (actual)
238
Serious AEs
2.1%
Results posted
Apr 2026
Primary outcome: Primary: Time From Randomisation to Next Hospital Readmission or Death (All Cause) — 25.7; 24.4 Weeks — p=0.811

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Mepolizumab (Drug); Placebo (Drug)
Age
Adult, Older Adult · 40+ yrs
Sex
All
Sponsor
University of Leicester
Primary completion
Jun 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Time From Randomisation to Next Hospital Readmission or Death (All Cause)
25.7; 24.4 0.811
SECONDARY
Total Number of Hospital Readmissions All Cause Over 48 Weeks
1.77; 1.54 0.505
SECONDARY
Total Number of Moderate Exacerbations Over 48 Weeks
2.22; 1.83 0.140
SECONDARY
Total Number of Severe Exacerbations Over 48 Weeks
1.20; 0.91 0.263
SECONDARY
Total Number of Exacerbations Over 48 Weeks
3.42; 2.74 0.054
SECONDARY
Time From Randomisation to Next Hospital Readmission or Death Due to a Respiratory Cause
24.4; 25.7 0.811
SECONDARY
Time From Randomisation to Treatment Failure
10.0; 12.9 0.849
SECONDARY
Hospital Readmission (Respiratory Cause)
55; 52 0.759
SECONDARY
Time From Randomisation to Next Hospital Readmission (All Cause)
27.9; 24.4 0.938
SECONDARY
Death (All Cause)
11; 9 0.705
SECONDARY
Death (Respiratory Cause)
8; 5 0.432
SECONDARY
Extended Medical Research Council Dyspnoea Score (eMRC)
5.0; 5.0; 4.0; 4.0; 4.0; 4.0 0.81
SECONDARY
St George's Respiratory Questionnaire (SGRQ)
72.0; 69.8; 66.2; 65.5; 64.6; 64.3 0.726
SECONDARY
COPD Assessment Tool (CAT)
26.1; 25.2; 23.9; 22.3; 23.8; 23.6 0.730
SECONDARY
Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS)
41.2; 42.9; 43.3; 44.9; 43.2; 44.7 0.789
SECONDARY
London Chest Activities of Daily Living Questionnaire (LCADL)
28.9; 27.6; 26.5; 24.7; 24.8; 24.6 0.563
SECONDARY
Short Physical Performance Battery (SPPB)
7.0; 7.0; 7.0; 8.5; 8.0; 8.0 0.03 sig
SECONDARY
Handgrip Strength
24.9; 27.3; 25.6; 27.6; 25.1; 27.4 0.913
SECONDARY
Percentage Sputum Eosinophil Count (Inflammatory Markers)
0.68; 0.75; 0.84; 0.47; 0.90; 0.48 0.002 sig
SECONDARY
Total Serum Eosinophil Count (Inflammatory Markers)
0.13; 0.15; 0.24; 0.08; 0.28; 0.07 <0.001 sig
SECONDARY
Adverse Events (AEs)
91; 91; 28; 27 0.070
SECONDARY
Serious Adverse Events (SAEs)
3; 2; 116; 116 0.686
SECONDARY
Pre Dose Systolic Blood Pressure (mmHg)
130.2; 129.7 0.585
SECONDARY
Post Dose Systolic Blood Pressure (mmHg)
128.1; 127.4 0.580
SECONDARY
Pre Dose Diastolic Blood Pressure (mmHg)
73.2; 73.1 0.506
SECONDARY
Post Dose Diastolic Blood Pressure (mmHg)
71.9; 72.3 0.729
SECONDARY
Pre Dose Heart Rate (Beats Per Minute)
81.4; 81.8 0.423
SECONDARY
Post Dose Heart Rate (Beats Per Minute)
79.8; 79.6 0.240
SECONDARY
Pre Dose Temperature (°C)
36.4; 36.4 0.981
SECONDARY
Post Dose Temperature (°C)
36.5; 36.5 0.946

Summary

This is a single-centre, double-blinded, randomised, placebo controlled trial comparing mepolizumab 100mg versus placebo in patients with eosinophilic COPD, started following their index admission to hospital.

Eligibility Criteria

Inclusion Criteria

  • Symptoms typical of COPD when stable (baseline eMRC dyspnoea grade 2 or more).
  • A clinician defined exacerbation of COPD requiring admission to hospital.
  • Serum eosinophil count of ≥ 300 cells/μL either at time of admission or at any one time in the preceding 12 months.
  • Smoking pack years ≥10 years.
  • Age ≥ 40 years.
  • Established on inhaled corticosteroids (ICS) prior to this admission.
  • Willing and able to consent to participate in trial.
  • Able to understand written and spoken English.

Exclusion Criteria

  • COPD patients without eosinophilia (defined as persistently < 300 cells/μL within the last 12 months).
  • Other conditions that may be the cause of eosinophilia (such as hypereosinophilic syndrome, eosinophilic granulomatosis, eosinophilic oesophagitis or parasitic infection).
  • Patients whose treatment is considered palliative (life expectancy < 6 months).
  • Other respiratory conditions including active lung cancer, interstitial lung disease, primary pulmonary hypertension or any other conditions that in the view of the investigator will affect the trial.
  • Known history of anaphylaxis or hypersensitivity to mepolizumab or any of the excipients (sucrose, sodium phosphate dibasic heptahydrate, polysorbate 80).
  • Unstable or life-threatening cardiac disease including myocardial infarction or unstable angina in the last 6 months, unstable or life-threatening cardiac arrhythmia requiring intervention in the last 3 months and New York Heart Association (NYHA) Class IV heart failure.
  • Decompensated liver disease or cirrhosis.
  • Pregnant, breastfeeding, or lactating women. Women of child-bearing potential must agree to use appropriate methods of birth control and have a negative blood serum pregnancy test performed after randomisation but prior to first dosing with randomised treatment.*
  • Participation in an interventional clinical trial within 3 months of visit 1 or receipt of any investigational medicinal product within 3 months or 5 half-lives.
  • Known blood born infection (e.g. HIV, hepatitis B or C).
  • Women of child bearing potential (WOCBP) - A woman is defined as being of childbearing potential (WOCBP), i.e. fertile, following menarche and until becoming post-menopausal, unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04075331). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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