3TR Asthma Biologics Cohort (ABC) Study
The 3TR-ABC study is a multicentre observational prospective cohort study platform that follows patients with severe asthma from the start of biological therapy and three years onwards. In the 3TR-ABC platform, individual studies are conducted on specific biologics, using aligned study designs. The aim of the study is to assess response to treatment and examine clinical characteristics, biomarkers, and immunological mechanisms related to response, including remission and non-response, that might be new targets or…
Conditions studied
Severe Asthma
About this study
The 3TR-ABC study is a multicentre observational prospective cohort study platform that follows patients with severe asthma from the start of biological therapy and three years onwards. In the 3TR-ABC platform, individual studies are conducted on specific biologics, using aligned study designs. The aim of the study is to assess response to treatment and examine clinical characteristics, biomarkers, and immunological mechanisms related to response, including remission and non-response, that might be new targets or explanations for insufficient treatment. Patients will be extensively characterized at baseline and then followed throughout the years with formal clinical and biological assessment at 4, 16, 52 weeks, and 2, 3 years. Based on the response to treatment, patients will be stratified into remission, clinical responders, and non-responders, and pre-treatment biomarker profiles obtained at the baseline visit will be compared, as well as the immunological response to treatment. Healthy individuals and patients with mild/moderate controlled asthma are included as reference groups and will undergo the same baseline visit as patients with severe asthma. Several bio-samples, to perform multi-omic analysis, will be taken to examine biological pathways associated with response and non-response to biologics.
Primary outcomes
- Change in Asthma Control Questionnaire 5 (ACQ-5) score (1 year, 2 and 3 years)
- Change in post- broncodilator Forced Expiratory Volume after 1 second (FEV1) (1 year, 2 and 3 years)
- Absense of exacerbations (1 year, 2 and 3 years)
- No usage of oral corticosteroids in the previous 12 months (1 year, 2 and 3 years)
Eligibility information
Study locations
- Bispebjerg Hospital, Copenhagen, 2400 Denmark
- Amsterdam University Medical Center, Amsterdam, North Holland 1105AZ Netherlands
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-11-01.