Taiwan Severe Asthma Biologic Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorTaichung Veterans General Hospital

About this trial

This is a prospective multi-centers cohort study for registration adult patients with severe asthma and were reimbursed biologics treatment in Taiwan.

The goal of this observational study is to discover the real-world effectiveness, the impact of initiating, switching of biologics, and the possible prediction factors for selecting the best treatment option for patients.

The main question\[s\] it aims to answer are:

1. Determine risk factors associated with poor asthma control. 2. Support the development of effectiveness and safety of therapeutic principles 3. To discover the real-world effectiveness of different biologics ( Clinical remission) 4. To discover the impact of initiating biologics for severe asthma patients. 5. To evaluate the prevalence of biologics switching and its benefits for patients. 6. To compare the achievement rate of clinical remission among different biologics.

Participants who are treated either with omalizumab, mepolizumab, benralizumab dupilzumab or Tezepelumab after January 1, 2020 will be included in the study.

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • Biological Treatment for severe asthma patients

Treatment groups

500 Participants
are divided into 5 treatment groups

Sponsors and collaborators

Taichung Veterans General Hospital

Lead sponsor

E-DA Hospital

Collaborator

National Cheng-Kung University Hospital

Collaborator

National Yang Ming Chiao Tung University Hospital

Collaborator

Chang Gung Memorial Hospital

Collaborator