Study of dupilumab injections to reduce airway inflammation in adults aged 40-85 with chronic obstructive pulmonary disease

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What is this study about?

This study focuses on patients with Chronic Obstructive Pulmonary Disease (COPD), a long-term lung condition that causes breathing difficulties. The research examines the effects of dupilumab, given as an injection under the skin, compared to a placebo. The purpose is to evaluate how this medication affects inflammation in the airways, particularly looking at mucus buildup in the lungs.

The study involves patients who have moderate to severe COPD and show specific signs of inflammation in their blood. During the study, participants receive either dupilumab (also known as SAR231893) or a matching placebo as injections under the skin for 24 weeks. The medication is provided in pre-filled syringes, and participants continue taking their regular COPD medications throughout the study.

The research uses special lung imaging techniques to examine how the treatment affects mucus in the airways. High-resolution Computed Tomography (HRCT) scans are used to look at changes in the lungs over the course of treatment. The study also monitors the safety of the treatment and any changes in breathing ability.

1 Initial assessment

You will undergo an evaluation to confirm your eligibility for the study, including verification of chronic obstructive pulmonary disease (COPD) diagnosis

Your medical history will be reviewed, including smoking history of at least 10 pack-years

Blood tests will be performed to check your eosinophil levels (type of white blood cells)

A high-resolution computed tomography (HRCT) scan will be performed to assess mucus in your lungs

2 Treatment assignment

You will be randomly assigned to receive either dupilumab or placebo

The medication will be provided as an injection under the skin (subcutaneous use)

You will continue your regular COPD medications throughout the study

3 Treatment period

The treatment period will last 24 weeks

You will receive regular injections of either dupilumab or placebo

Your current COPD medications will continue, including triple therapy (three different types of inhaled medications) or dual therapy if needed

4 Monitoring and assessments

Regular tests will be performed to measure your lung function

You will undergo forced oscillation technique (FOT) tests to measure airway resistance

Additional HRCT scans will be performed to track changes in mucus levels and airway wall thickness

Any side effects or health changes will be monitored and recorded throughout the study

5 Final evaluation

At week 24, final assessments will be performed

These will include HRCT scans, lung function tests, and blood tests

The results will be compared to your initial measurements to evaluate the treatment effects

Who Can Join the Study?

  • Must be a current or former smoker with a history of smoking at least 10 pack-years (equivalent to smoking 1 pack of cigarettes per day for 10 years)
  • Must have moderate-to-severe breathing condition with specific lung function test results showing:
    • Reduced breathing capacity after using bronchodilator medication
    • Lung function between 30% and 70% of normal predicted values
  • Must have either:
    • Significant breathlessness (grade 2 or higher on breathing difficulty scale), or
    • Score of 10 or higher on COPD assessment test measuring daily symptoms
  • Must have frequent or severe episodes of symptom worsening
  • Must be using three types of inhaled medications for at least 3 months, with stable dosing for at least 1 month before study start (or two types if unable to use inhaled steroids)
  • Must have elevated levels of specific white blood cells (eosinophils) showing either:
    • 300 or more cells per microliter at screening, or
    • 150 or more cells per microliter at screening with previous history of 300 or more cells in the past year
  • Must have a mucus score of 3 or higher on medical imaging
  • Must be an adult (18 years or older)
  • Can be either male or female

Who Cannot Join the Study?

  • Previous participation in a clinical trial involving dupilumab (an injectable medication for treating certain inflammatory conditions)
  • Having any serious or active infections, including tuberculosis or hepatitis B
  • History of severe allergic reactions to injectable medications
  • Current pregnancy or breastfeeding
  • Significant liver or kidney disease
  • Active cancer or cancer treatment within the past 5 years
  • Use of other biologic medications (specialized drugs that target specific parts of the immune system) within the past 4 months
  • Uncontrolled heart disease or high blood pressure
  • History of drug or alcohol abuse within the past year
  • Mental health conditions that could interfere with study participation
  • Any condition that, in the opinion of the study doctor, would make participation unsafe
  • Unable or unwilling to undergo required HRCT scans (detailed X-ray imaging of the chest)
  • Unable to follow study procedures or attend scheduled visits

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Canisius Wilhelmina Ziekenhuis Nijmegen The Netherlands
Alergologia Plus Sp. z o.o. Poznan Poland
Centrum Medycyny Oddechowej Mroz Sp. j. Bialystok Poland
Infer-Med Kft. Pecs Hungary
Azienda Unita’ Locale Socio Sanitaria N. 2 Marca Trevigiana Treviso Italy
IKF Pneumologie GmbH & Co. KG Frankfurt Germany
University Of Debrecen Debrecen Hungary
Velocity Clinical Research Luebeck GmbH Luebeck Germany
Azienda Ospedaliero-Universitaria San Luigi Gonzaga Orbassano Italy
Region Skane Skanes Universitetssjukhus Lund Sweden
Karolinska University Hospital Solna Sweden
Stichting Radboud University Medical Center Nijmegen The Netherlands
Hospital Universitario Fundacion Jimenez Diaz Madrid Spain
Hospital Universitario Quironsalud Madrid Pozuelo De Alarcon Spain
Centre Hospitalier Universitaire De Montpellier Montpellier France
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Aalborg University Hospital Aalborg Denmark
Kepler Universitaetsklinikum GmbH Linz Austria
Sint Franciscus Vlietland Groep Stichting Rotterdam The Netherlands
Centre Hospitalier Lyon Sud Pierre Benite France
Hopital Beaujon Clichy France
Universita’ Degli Studi Di Ferrara Ferrara Italy
Queen Silvia Childrens Hospital – Sahlgrenska University Hospital – Vaestra Goetalandsregionen Gothenburg Sweden
Stadt Wien Wiener Gesundheitsverbund Vienna Austria
Spaarne Gasthuis Hoofddorp The Netherlands
Ctwskl Hyvjyrhhzjw Ukrotnntbryct Rpkrg Reims France
Uuunrcpunxgr Mohgalp Chlgnle Gbhvchwkp Groningen The Netherlands
Hgpdnmep Ucgvhqftzchys Mpiytcj Dc Vhoqzccrbp Santander Spain
Ohxjgvyvpmpv Cjfqcrt Mzixkfht Aiuk Ofqyk Cwiidc Kqwxorvze Celweg scwn Ostrowiec Swietokrzyski Poland
Cecgypywt Kmtr Hajdunanas Hungary
Pagfzd Rhcrdhtvjbi Hwewxe Sbvk Barcelona Spain
Akicpddqvy Pgknivde Hycrxrfp Do Mkefqkvle Marseille France
Anvocam Oioaqknkqdi Utmjlmebaobqs Spdraf Siena Italy

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not yet recruiting
01.10.2025
Denmark Denmark
Recruiting
01.10.2025
France France
Recruiting
01.10.2025
Germany Germany
Not yet recruiting
01.10.2025
Hungary Hungary
Recruiting
01.10.2025
Italy Italy
Recruiting
01.10.2025
Poland Poland
Recruiting
01.10.2025
Spain Spain
Recruiting
01.10.2025
Sweden Sweden
Not yet recruiting
01.10.2025
The Netherlands The Netherlands
Recruiting
01.10.2025

Trial locations

Investigated drugs:

Dupilumab is a medication used to treat inflammation in the airways. It works by blocking certain proteins in the body that cause inflammation. In this trial, it is being studied for its effects on reducing mucus plugging in the lungs of patients with chronic obstructive pulmonary disease (COPD). The medication helps decrease inflammation in the airways and may improve breathing by reducing the amount of mucus that builds up in the lungs.

Respiratory tract disease – A condition affecting the airways and other structures of the respiratory system, from the nasal passages to the lungs. It involves the accumulation of mucus in the airways, which can lead to breathing difficulties. The condition can cause changes in airway wall thickness and affect normal respiratory function. Respiratory tract disease often involves increased airway resistance and changes in lung tissue that can be observed through medical imaging. The condition may be characterized by ongoing inflammation of the respiratory passages.

Trial ID:
2025-521268-37-00
Protocol code:
LPS18583
Trial Phase:
Therapeutic confirmatory (Phase III)

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