Phase 3
N=238
Mepolizumab for COPD Hospital Eosinophilic Admissions Pragmatic Trial
COPD · Eosinophilia
Bottom Line
View on ClinicalTrials.gov: NCT04075331 ↗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
| Outcome | Result | p-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.
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.