Clinical trial Recruiting at 1 site Observational Ages 18 and up

Registry for adults with severe asthma receiving biologic treatments in Taiwan

Official title: Taiwan Severe Asthma Biologic Registry

Run by Taichung Veterans General Hospital · NCT06456450 · Data updated 2026-11-12

This study is tracking adults with severe asthma in Taiwan who are using biologic treatments to see how well they work and what factors might help choose the best options.

More Asthma trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment500 (estimated)
SponsorTaichung Veterans General Hospital
Academic / other
Drugs / interventionsomalizumab, mepolizumab, benralizumab, dupilzumab, Tezepelumab
Locations1 site (Taichung)
StatusRecruiting
StartedNovember 11, 2023
Main results expectedFebruary 28, 2043
Study endsFebruary 28, 2043
Registry record updatedMay 19, 2026
Trial IDNCT06456450 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults over 18 years old with severe asthma who have started biologic treatment after January 1, 2020.

Probably not a fit

Patients with a history of biologic treatment prior to January 1, 2020, or those with significant comorbid pulmonary diseases may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to register adult patients with severe asthma who are receiving biologic treatments in Taiwan. It will evaluate the real-world effectiveness of these treatments, the impact of initiating or switching biologics, and identify potential factors that predict the best treatment options. The study will also assess risk factors associated with poor asthma control and compare the clinical remission rates among different biologics. Participants will include those treated with omalizumab, mepolizumab, benralizumab, dupilumab, or Tezep.

Why it matters

Potential benefit: If successful, this study could provide insights into the most effective biologic treatments for severe asthma, leading to improved patient outcomes.

How similar studies have gone: Other studies have shown success in evaluating the effectiveness of biologics for severe asthma, making this approach both relevant and supported by prior findings.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Provision of informed consent prior to any study specific procedures.
* Patient should be reviewed as well as confirmed by the National Health Insurance Administration (NHIA) or by the study board member as a Severe Asthma case.
* Female and male aged over 18 years old.
* Patients who are treated either with omalizumab, mepolizumab, or benralizumab after January 1, 2020.

Exclusion Criteria:

* Lack of informed consent for participation.
* History of Biologic usage before January 1, 2020, should be ruled out.
* The washout period should be at least 12 months. In other words, the enrolled patients should have no experience in receiving a biological treatment or in participating relative clinical trial before his/her biologic initiation.
* Comorbid pulmonary diseases (e.g.: Chronic Obstructive Pulmonary Disease, Bronchiectasis, Pulmonary Fibrosis, etc.) or risk factors (e.g.: smoking or environmental exposure, etc..) that could be associated with pulmonary or systemic diseases, other than Asthma.

Where it's running

  • Taichung Veterans General Hospital
    Taichung, Taiwan
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.