Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06224634

The Effect of Anti-IL17 on Airway Hyperresponsiveness and Resistance

Led by Copenhagen University Hospital, Hvidovre · Updated on 2025-03-18

74

Participants Needed

1

Research Sites

126 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

The Effect of Anti-IL17 on Airway Hyperresponsiveness and Resistance

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients planning to start treatment with anti-IL-17 antibodies
Not Eligible

You will not qualify if you...

  • Current pregnancy
  • FEV1 less than 1.5L or less than 60% of predicted value
  • 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

AI-Screening

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Trial Site Locations

Total: 1 location

1

Respiratory Research Unit Hvidovre Department of Respiratory Medicine, Copenhagen University Hospital

Hvidovre, Capital Region, Denmark, 2650

Actively Recruiting

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Research Team

J

Jonas A Baekdal, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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