MedPath

A Randomized, Double-blind, Placebo-controlled, Parallel-group, 52-week Pivotal Study to Assess the Efficacy, Safety, and Tolerability of Dupilumab in Patients with Moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD) with Type 2 inflammatio

Phase 3
Recruiting
Conditions
chronic bronchitis
10006436
Registration Number
NL-OMON54320
Lead Sponsor
Genzyme Europe BV
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
28
Inclusion Criteria

Participants with a physician diagnosis of COPD who meet the following criteria
at screening:
- Current or former smokers with a smoking history of >=10 pack-years
- Moderate to severe COPD (post-bronchodilator FEV1/FVC ratio <0.70 and
post-bronchodilator FEV1 % predicted >30% and <=70%)
- Medical Research Council (MRC) Dyspnea Scale grade >=2
- Patient-reported history of signs and symptoms of chronic bronchitis (chronic
productive cough) for 3 months in the year up to screening in the absence of
other known causes of chronic cough
- Documented history of high exacerbation risk defined as exacerbation history
of >=2 moderate* or >=1 severe** within the year prior to inclusion. At least one
exacerbation should have occurred while the patient was taking ICS/LAMA/LABA
(or LAMA/LABA if ICS is contradicted). Moderate exacerbations are recorded by
the Investigator and defined as AECOPD that require either systemic
corticosteroids (intramuscular (IM), intravenous, or oral) and/or antibiotics.
One of the two required moderate exacerbations has to require the use of
systemic corticosteroids. Severe exacerbations are recorded by the Investigator
and defined as AECOPD requiring hospitalization or observation >24 hours in
emergency department/urgent care facility
- Background triple therapy (ICS + LABA + LAMA) for 3 months prior to
randomization with a stable dose of medication for >=1 month prior to Visit 1;
Double therapy LABA + LAMA allowed if ICS is contraindicated
- Evidence of Type 2 inflammation: Patients with blood eosinophils >=300
cells/microliter at Visit 1

Exclusion Criteria

- COPD diagnosis for less than 12 months prior to randomization
- Participants with current diagnosis of asthma according to the Global
Initiative for
Asthma (GINA) guidelines, or documented history of asthma
- Significant pulmonary disease other than COPD (eg, lung fibrosis,
sarcoidosis, interstitial
lung disease, pulmonary hypertension, bronchiectasis, Churg-Strauss Syndrome,
etc) or another diagnosed pulmonary or systemic disease associated with
elevated peripheral eosinophil counts
- Cor pulmonale, evidence of right cardiac failure
- Long-term treatment with oxygen >4.0 L/min OR if a participant requires more
than
2.0 L/min in order to maintain oxygen saturation >88%
- Hypercapnia requiring BiPAP
- AECOPD as defined in inclusion criteria within 4 weeks prior to or during the
screening period
- Respiratory tract infection within 4 weeks prior to screening, or during the
screening period
- History of, or planned pneumonectomy or lung volume reduction surgery.
Patients who are participating in the acute phase of a pulmonary rehabilitation
program, ie, who started rehabilitation <4 weeks prior to screening (Note:
patients in the maintenance phase of a rehabilitation program can be included)
- Diagnosis of a-1 anti-trypsin deficiency

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>- Annual rate of acute COPD exacerbation (AECOPD)</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>- Change in SGRQ<br /><br>- Improvement in SGRQ<br /><br>- Change in pre-bronchodilator FEV1 from baseline to Week 52<br /><br>- Change in pre-bronchodilator FEV1 from baseline to time points up to Week 44<br /><br>- Change in post-bronchodilator FEV1 lung function<br /><br>- Change in forced expiratory flow (FEF) 25-75%<br /><br>- Annualized rate of severe AECOPD<br /><br>- Time to first AECOPD<br /><br>- Adverse events<br /><br>- Potentially clinically significant abnormality (PCSA) in laboratory tests<br /><br>- Anti-drug antibodies</p><br>
© Copyright 2025. All Rights Reserved by MedPath