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Studies how anti-IL-17 treatment affects airway tightness in adults

Observes airway changes in adults with skin or joint disease starting anti-IL-17 treatment.

Plain-language title generated from the registry record
Registry title: The Effect of Anti-IL17 on Airway Hyperresponsiveness and Resistance

Key facts

Where
Hvidovre, DenmarkSee the site

Where in Denmark

  • Respiratory Research Unit Hvidovre Department of Respiratory Medicine, Copenhagen University HospitalHvidovre, DenmarkTaking people

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Trial details

Who runs it
Copenhagen University Hospital, Hvidovre
Trial code
NCT06224634
Record updated
18 March 2025
Original description
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.Read full original descriptionShow less

The Effect of Anti-IL17 on Airway Hyperresponsiveness and Resistance: a Longitudinal Cohort 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.

Inclusion: Patients planning to start treatment with anti-IL-17 antibodies.

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

ClinicalTrials.gov NCT06224634