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NCT07049978Completed

Long-term Effect of Dupilumab in N-ERD

Long-term Effect of Dupilumab on Acetylsalicylic Acid (ASA) Intolerance and Its Mechanisms in Patients With Non-steroidal Anti-inflammatory Drug-exacerbated Respiratory Disease (N-ERD)

Source: ClinicalTrials.gov · Last updated 7 Oct 2026

Brief summary (registry, in English)

This prospective observational study investigates the long-term effects of Dupilumab in patients with NSAID-exacerbated respiratory disease (N-ERD). The study assesses changes in ASA tolerance, clinical parameters, inflammatory biomarkers, quality of life, and nasal microbiome during ongoing treatment with Dupilumab. All participants are receiving Dupilumab as part of standard clinical care.

Status (registry)
Completed
Study type
Observational
Enrollment
15 (actual)
First submitted
25 Jun 2025
Start date
1 Sept 2025
Primary completion date
7 May 2026
Lead sponsor
Medical University of Vienna
Diseases
Asthma
NCT number
NCT07049978

What you commit to

  • Study type: Observational
  • Participants enrolled: 15
  • From 1 Sept 2025 to the primary completion date, 7 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Need for systemic corticosteroid therapy 1 month prior to screening visit
  • Previous anaphylaxis and contraindications against ASA as outlined in the official prescribing information.

Other illness

  • History of malignancy or immunodeficiency
  • Chronic obstructive lung disorders (COPD), other obstructive lung disorders (bronchiolitis)
  • Eosinophilic pneumonia and Churg-Strauss Syndrome

Lab values

  • Clinically significant abnormal laboratory values and active infection (Tbc, HIV, hepatitis A/B/C)

Other

  • Pregnancy (as determined by urine ß-HCG test)

Who the study is looking for

  • Participated previously in our preliminary study (EK 1044/2020) and continued Dupilumab treatment since then. Long-term use of Dupilumab since the preliminary study will be assessed based on patient self-report, as there is currently no clinical test or laboratory parameter available to objectively verify treatment duration.
  • Signed and dated informed consent has been obtained
  • Current therapy with Dupilumab

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Medical University of Vienna
Coordinator of this site? Confirm its status
ViennaAustriaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.