COPD Trial, Recruiting NCT06724848 Sponsor: AstraZeneca Condition: COPD
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COPD Trial, Recruiting

NCT06724848
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are able to sign an informed consent form agreeing to take part in the study.
  • People who are able to complete a specific breathing test (measuring how much air can be forced out of the lungs in one second) that meets recognised international standards.
  • People who are able and willing to follow the study requirements, including being able to read, write, and understand the language used in the study questionnaires.
  • People who are already taking part in other non-treatment research studies may still be considered for this trial.

Who may not be able to join:

  • People who have had a problem with alcohol or drug misuse in the past year, if the responsible doctor believes this would make participation unsafe.
  • People who are not able to think clearly or make decisions at the time of signing the consent form.
  • People who have unusual results from vital sign checks, heart tests (ECG), or blood/lab tests at the screening visit that the investigator believes could affect the study or the person's safety.
  • People who currently have a diagnosis of asthma.
  • People who have a significant lung disease beyond what is being studied (confirm with trial site).
  • People who have had a flare-up of their COPD in the two weeks before enrolling or during the screening period.
  • People who have had most or all of a lung surgically removed (removal of a single lobe or smaller section may be acceptable); or who have had a procedure to reduce lung size in the six months before enrolling; or who are expected to need such a procedure during the study.
  • People who have unstable medical conditions (confirm with trial site for specific details).
  • People who currently have, or have had, cancer in the past five years — with limited exceptions for certain treated skin cancers or cervical changes treated successfully more than one year before enrolling. People with suspected or undefined growths are also excluded.
  • People who have a terminal illness, organ failure, or who are otherwise considered by the study team to be unsuitable for participation.
  • People who have received a biologic medicine — whether an approved treatment or an experimental one — within the past three months or within five half-lives of the medicine before the first study visit, whichever period is longer.
  • People who are pregnant.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 1-877-240-9479

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
5 June 2024
Est. completion
21 October 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Medical History; Occupation; Birth Status; Place of residence; Smoking history and status; Family history; Exacerbation/respiratory history and event; COPD related HRU; SGRQ; CAT; MARS-5 (only applicable for COPD cohort); Variables in COPD related medication, changes in medication; FEV1 %; FEV1 /FVC; Forced Osc; FEF25-75; DLCO; LAAinsp-950%; LAAexp-856%; WA%; Inflammatory differentials and counts in blood and BALF; Inflammatory cell infiltration; MUC5B/MUC5AC; IL-33/ST2 complex; IL-33; Air trapping index; hsCRP; Transcriptomic test in nasal, bronchial brushings, biopsies and BALF asmples; Prot...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov