RecruitingPhase 2NCT05507242

Effects of Blocking TSLP on Airway Inflammation and the Epithelial Immune-response to Exacerbation Triggers in Patients With COPD

Effects of Blocking TSLP on Airway Inflammation and the Epithelial Immune-response to Exacerbation Triggers in Patients With COPD A Randomized Double-blind, Placebo-controlled Trial of Tezepelumab UPSTREAM-COPD


Sponsor

Asger Sverrild

Enrollment

80 participants

Start Date

Oct 25, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

A phase 2, multicentre, randomized, double-blind, placebo-controlled, parallel group study to evaluate the effect of tezepelumab on airway inflammation in patients with COPD.


Eligibility

Min Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This study tests a drug that blocks a protein called TSLP, which may trigger inflammation in the airways of people with COPD (chronic obstructive pulmonary disease — a lung condition that causes breathing difficulty). Researchers want to see if this drug reduces flare-ups and airway inflammation. **You may be eligible if...** - You are 40 years or older and have been diagnosed with COPD - You have smoked at least 10 pack-years (e.g., 1 pack a day for 10 years, whether current or ex-smoker) - Your breathing test results fall within a specific range showing moderate-to-severe airflow obstruction - You are already on maintenance inhalers (combinations of LAMA, LABA, and/or ICS) - You have had at least one COPD flare-up in the past year requiring steroids or antibiotics **You may NOT be eligible if...** - You have asthma or another lung disease as your primary diagnosis - You have had a major COPD flare-up in the past 6 weeks - You have significant heart, liver, or immune system problems - You are currently smoking and unwilling to try to quit - You are taking certain medications that could interact with the study drug Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALTezepelumab

Tezepelumab 210 mg for 20 weeks (5 doses in total, 4-week intervals), administered subcutaneously

OTHERPlacebo

Placebo subcutaneous injection for 20 weeks (5 doses in total, 4-week intervals)


Locations(2)

Research site

Copenhagen, Denmark

Research site

Leicester, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT05507242


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