Skip to content
Clinical Trials – home
Recruiting

A Study of Depemokimab Compared to Placebo in Adults with Chronic Obstructive Pulmonary Disease and Type 2 Inflammation

Fast replyRegistered drugNo placebo
Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

What is this trial about?

A plain-language summary of the goals, design and what participants do

This study is looking at Chronic Obstructive Pulmonary Disease, which is a lung condition that makes it hard to breathe and causes symptoms like coughing and shortness of breath. The study will test a medication called depemokimab, which is given as an injection under the skin. Some people in the study will receive depemokimab while others will receive placebo. People taking part will also continue using their regular inhaled medicines, which include salbutamol for quick relief of breathing problems and a combination of inhaled medications that help keep the airways open and reduce inflammation in the lungs. The study will also use a sterile 0.9% sodium chloride solution, which is a salt water solution.

The purpose of the study is to find out if depemokimab works better than placebo in treating people with this lung disease who have a type of inflammation called Type 2 inflammation. The study will look at whether the medication can reduce the number of times symptoms suddenly get worse, which doctors call exacerbations. These are times when breathing problems become much worse and may need treatment with antibiotics or steroid pills, or sometimes even a visit to the emergency room or hospital.

During the study, people will receive treatment for up to 104 weeks, which is about two years. The doctors will check how often breathing problems get worse, how long it takes before problems get worse, and how the disease affects daily life and breathing symptoms. The study will compare results between people receiving depemokimab and those receiving placebo to see if the medication helps reduce flare-ups and improves quality of life for people with this lung condition.

The research process

The trial runs in 5 steps – from screening to follow-up. Each step says what happens and what the team monitors.

  1. Step 1

    Initial treatment period begins

    Upon joining the study, you will be randomly assigned to receive either depemokimab or placebo. This is a double-blind study, which means neither you nor your doctor will know which treatment you are receiving.

    You will receive your assigned treatment through subcutaneous injection, which means the medication will be injected under your skin.

    Throughout the study, you will continue taking your regular inhaled medications for chronic obstructive pulmonary disease. These include your inhaled corticosteroid, long-acting muscarinic receptor antagonist, and long-acting beta2-adrenergic receptor agonist.

  2. Step 2

    Rescue medication availability

    You will have access to salbutamol sulfate as a rescue medication. This medication is available as an inhalation powder with a dose of 100 micrograms per inhalation.

    The product name is Novolizer Salbutamol. You should use this medication when you experience breathing difficulties or symptoms that require immediate relief.

    This rescue medication is taken through inhalation, meaning you breathe it in through your mouth using the inhaler device.

  3. Step 3

    Regular monitoring at Week 52

    At Week 52 of the study, specific assessments will be conducted to measure how the treatment is working.

    You will complete the St. George's Respiratory Questionnaire, which is a set of questions about how your lung condition affects your daily life. Your answers at this point will be compared to your answers at the beginning of the study.

    You will also complete the Evaluating Respiratory Symptoms questionnaire, which asks about your breathing symptoms. This will also be compared to your baseline responses.

  4. Step 4

    Ongoing assessment throughout the study

    Throughout the entire study period, your breathing function will be monitored. This includes measurements of how much air you can breathe out in one second, called forced expiratory volume in one second.

    Any worsening of your condition, called exacerbations, will be recorded. These are episodes when your symptoms get worse and may require additional treatment.

    The study will track whether these exacerbations are moderate, meaning they require treatment with antibiotics or steroids, or severe, meaning they require a visit to the emergency department or hospital admission.

  5. Step 5

    Study completion

    The study is expected to continue until the end of 2029. Your individual participation duration will be determined by the study protocol.

    Throughout your participation, the study will evaluate how well the treatment reduces the frequency of exacerbations and improves your quality of life and breathing symptoms.

    Safety monitoring will occur throughout the entire study period to assess any side effects or adverse reactions to the treatment.

Who can join the trial?

10 criteria

  • You must be between 40 and 80 years old when you sign the consent form to join the study
  • You must have a high number of eosinophils in your blood. Eosinophils are a type of white blood cell that can cause inflammation in your airways
  • You must have moderate to severe COPD (a lung disease that makes it hard to breathe) with frequent worsening of symptoms, which means:
    • You have been diagnosed with COPD for at least 1 year
    • A breathing test shows that your lung function is reduced, with results showing your FEV1 (the amount of air you can breathe out in one second) is between 30% and 80% of what is expected for someone your age and size
    • You have had at least 2 moderate flare-ups or 1 severe flare-up of your COPD symptoms in the past 12 months before joining the study
    • Your CAT score must be 10 or higher at the first visit. The CAT is a questionnaire that measures how much COPD affects your daily life
    • You must be a current or former cigarette smoker with a smoking history of at least 10 pack-years. A pack-year means smoking one pack of cigarettes per day for one year
    • You must be using the best inhaler treatment for at least 6 months before joining the study. This treatment must include three types of medications: an inhaled corticosteroid (a medicine that reduces inflammation), a LAMA (a medicine that helps open your airways), and a LABA (another medicine that helps keep your airways open). These can be in separate inhalers or combined in one inhaler
    • Your body mass index (BMI) must be 16 or higher. BMI is a measure of body weight compared to height
    • Both men and women who meet certain requirements can participate in the study

Who cannot join the trial?

3 criteria

  • The source data does not contain specific exclusion criteria (reasons why patients cannot participate) for this clinical trial
  • Without detailed exclusion criteria information, it is not possible to list the specific conditions or situations that would prevent participation in this study
  • Exclusion criteria typically include things like other medical conditions, certain medications being taken, previous treatments, or test results that would make it unsafe or inappropriate for someone to join the study
Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.

We usually reply within a few days

Verified sites

All sites with verified contact details – recruitment status may not be available; ask directly

Trial locations

Where you can join this trial

Countries are shaded by recruitment status. Click a recruiting country to ask about joining there.

Recruiting
Not finding your country?

Not sure what to do next?

Joining a clinical trial can seem overwhelming. We guide you step by step, so you know exactly what to expect and how we support you through the process.

See the full process and FAQ

Investigated drugs

Depemokimab is an investigational medication being studied for the treatment of chronic obstructive pulmonary disease (COPD) in adults who have Type 2 inflammation. This medication is being tested to see if it can help improve the condition of people with this specific type of COPD. In this study, depemokimab will be compared against a placebo to determine how well it works and how safe it is for patients.

What is already known about the treatment

Depemokimab – Depemokimab is an investigational medication currently being studied in clinical trials and is not yet approved for general medical use. It is being tested as a treatment for chronic obstructive pulmonary disease (COPD) in patients who have Type 2 inflammation, which is a specific pattern of immune system activity that can worsen lung disease. The medication works by targeting and blocking certain proteins called interleukins that promote inflammation in the airways, helping to reduce swelling and improve breathing. Depemokimab belongs to a class of drugs called monoclonal antibodies, which are laboratory-made proteins designed to attach to specific targets in the body, and it is administered through injection.

Investigated diseases

Chronic Obstructive Pulmonary Disease – Chronic Obstructive Pulmonary Disease is a long-term lung condition that makes it difficult to breathe. The disease causes the airways to become narrowed and the air sacs in the lungs to lose their stretchiness. Over time, the lungs produce more mucus which can further block the airways. People with this condition often experience shortness of breath, persistent cough, and wheezing. The disease typically gets worse gradually over the years. Flare-ups, called exacerbations, can occur where symptoms suddenly become more severe.
Trial detailsLast updated 2 Oct 2026
Age18+ yearsPhasePhase IIITrial ID2024-520417-41-00Protocol code222725Estimated enrolment993 patientsSponsorGlaxosmithkline Research & Development Limited

sourced from the EU Clinical Trials Register and site verification

Want to learn more about this trial or check if you can participate?

Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.

Legal notice · Published by CTIN POLAND sp. z o.o., ul. rtm. Witolda Pileckiego 67/109, 02-781 Warsaw, Poland · KRS 0001111334 · REGON 528919042 · NIP 9512598637

© 2026 Clinical Trials EU – European Clinical Trials Information Network

GDPR compliance, ISO 9001 and ISO 27001 certified (LL-C Certification)

On this site, “treatment” means an investigational medicine being studied in a clinical trial. Its safety and efficacy for the use being studied have not yet been confirmed, some participants may receive a placebo or a comparator medicine, and taking part does not guarantee any health benefit. The decision to take part is made by the doctor at the research site. This site is for information only and does not replace medical advice.

This service is not affiliated with the European Commission, the EMA, or the official CTIS system. Most information comes from publicly available international clinical-trial registries, supplemented by data from academic sites, national regulators and commercial sponsors. On this site, “treatment” and “therapy” mean a medicine being tested in a clinical trial. Its safety and effectiveness in the use being studied are not yet confirmed, some participants may receive a placebo or a comparator, and taking part does not guarantee a health benefit. The doctor at the research site decides who can take part. This site provides information, not medical advice. Certain content and visual elements on this website have been generated or enhanced using artificial intelligence (AI).