Phase 3 study for people with COPD

Recruiting Phase 3

Sources: ClinicalTrials.gov Checked: 11 October 2026 Not medical advice

This trial at a glance

Status Recruiting
Phase Phase 3
Sponsor GlaxoSmithKline
Registry number NCT07177339
Started 20 October 2025 Today 16 October 2026 Estimated completion 30 April 2029

Where this trial is running

Trial sites and the status recorded for each
SiteCityState or countryStatus at this site
GSK Investigational Site Coffs Harbour NSW Recruiting
GSK Investigational Site Spearwood WA Recruiting

voxsanity.com.au · trial sites from public registries · registry record synced 11 October 2026 · not medical advice

Who can join

Age 40 Years to 75 Years
Sex Anyone, regardless of sex
Healthy volunteers Not accepted
Enrolment target 1196

The official eligibility criteria

Registry text, reproduced exactly. These are the words the trial's sponsor published on ClinicalTrials.gov. They have not been edited, shortened or rewritten, and they are written for researchers rather than for patients.

Inclusion Criteria:

* Male or eligible female participants

* Eosinophilic phenotype measured using Blood Eosinophil Count (BEC)

* Moderate to severe COPD, defined as

* A clinically documented history of COPD for at least 1 year

* A post-salbutamol Forced expiratory volume in one second (FEV1)/Forced vital capacity (FVC) ratio of less than (\<)0.70 and a post-salbutamol FEV1 greater than (\>)30 percent (%) and \<80% predicted normal values

* Elevated risk for exacerbations, defined as

* A well-documented history of only 1 moderate COPD exacerbation in the prior 12 months and

* The presence of risk factors for future exacerbations/deterioration such as:

* Modified Medical Research Council (mMRC) dyspnea score \>= 2

* COPD Assessment Test (CAT) \>= 15

* Post-bronchodilator FEV1 \< 50% predicted

* Chronic bronchitis

* Smoking status: Current or former cigarette smokers with a history of cigarette smoking of \>=10 pack-years at Screening.

* Dual (Inhaled corticosteroid (ICS)+ Long-acting beta2-adrenergic receptor agonist \[LABA\] or LABA+ Long-acting muscarinic receptor antagonist \[LAMA\]) or triple (ICS+LABA+LAMA) inhaler therapy as assessed by the investigator for at least 3 months

* Body mass index (BMI) \>=16 kilograms per square meter (kg/m\^2)

Exclusion Criteria:

* The Investigator must judge that COPD is the primary diagnosis accounting for the clinical manifestations of lung disease, and clinical manifestations of lung disease where primary diagnosis is not COPD are excluded

* Participants with a current or prior physician diagnosis of asthma

* Participants with childhood asthma are permitted, provided that childhood asthma has resolved before 18 years of age and has not recurred

* Other clinically significant lung disease: The Investigator must judge that COPD is the primary diagnosis accounting for the clinical manifestations of the lung disease.

* COPD severity: Participants with more than one moderate exacerbation or severe exacerbation in the past 12 months prior to Visit 1

* COPD stability: Participants with pneumonia, COPD exacerbation, or lower respiratory tract infection within the 4 weeks prior to Visit 1

* Lung resection: Participants with a history of, or plan for lung volume reduction surgery/endobronchial valve procedure

* Pulmonary rehabilitation: Participants in the acute phase of a pulmonary rehabilitation program within 4 weeks prior to Visit 1

* Chronic hypercapnia requiring non-invasive positive pressure ventilation (NIPPV) use including Bi-Level Positive Airway Pressure (BiPAP) or Continuous Positive Airway Pressure (CPAP) are excluded

* Continuous oxygen: Participants requiring oxygen supplementation for COPD

Dates on the record

Started 20 October 2025
Estimated completion 30 April 2029
Registry last updated 28 July 2026
Checked by Voxsanity 11 October 2026

Results, publications and the official record

Sources and dates

  • ClinicalTrials.gov – the record this page reformats
  • ClinicalTrials.gov processing date: 28 July 2026.
  • This page last checked by Voxsanity: 11 October 2026.

Voxsanity reformats data from public registries into this layout. It does not edit, interpret or add to what the registry published.

Not medical advice.

Individual trial records are refreshed on a rolling basis rather than all at once, so a record may be up to several weeks old. Each trial page and trial card shows the date its own record was last synced. Where a record has lagged, its status, sites and enrolment can differ from the current registry state in either direction, so check the registry link on the trial page before acting on them.

Letter for your doctor

A one-page summary of this trial to print or email to your GP. It carries the registry's own record of the trial and its eligibility criteria, and nothing Voxsanity has written about whether it suits you.