TTrialPathMatch Me to Trials
← Back to trials
RecruitingAsthma

The Effect of Anti-IL17 on Airway Hyperresponsiveness and Resistance

Eligible age

18+ yrs

Accepts

All genders

Locations

0 states

Healthy volunteers

Yes

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

This observational longitudinal cohort study aims to assess the effect of monoclonal antibodies targeting interleukin 17 (anti-IL-17) on airway hyperreactivity and airway resistance. The study involves adult participants suffering from dermatological or rheumatological illness, who are planning to start treatment with monoclonal antibodies targeting interleukin 17 as a part of the treatment of these diseases. The primary outcome of this study will be changes in airway hyperresponsiveness to methacholine challenge reported as response-dose-ratio before and after initiation of anti-IL17 treatment regardless of presence of respiratory disease. Furthermore, the potential effect of anti-IL-17 on airway resistance will be assessed using conventional spirometry for measuring changes in FEV1 and Airwave oscillometry. A reduced degree of airway hyperreactivity and airway resistance after initiating ani-IL-17 could indicate effectiveness of anti-IL-17 in asthma patients which would have to be examined further in a population of asthma patients.

Sponsor: Copenhagen University Hospital, Hvidovre

You may qualify if…

  • ✓ Patients planning to start treatment with anti-IL-17 antibodies

You may not qualify if…

  • ✕ Current pregnancy
  • ✕ FEV1 \< 1.5L or less than 60% of predicted value expected.
  • ✕ Previous anaphylactic shock or severe allergic reaction to medicine
  • ✕ Uncontrolled hypertension
  • ✕ Myocardial infarction or stroke within the last 3 months
  • ✕ Known aortic aneurysm
  • ✕ Recent eye surgery or risk of elevated intracranial pressure
  • ✕ Treatment with systemic corticosteroids within 6 weeks

Source: ClinicalTrials.gov · NCT06224634 · last updated 2025-03-18