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Taking people in Hollandia3. fázis

the BIRDIE trial

Key facts

Where
Rotterdam, HollandiaSee the site
Phase
3. fázis

Where in Hollandia

  • Sint Franciscus Vlietland Groep StichtingRotterdam, HollandiaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Sint Franciscus Vlietland Groep Stichting
Trial code
EU 2023-505839-12-01
Record updated
2025. december 3.
Original description
1. To evaluate if it is possible to extend the dosing interval of mepolizumab, driven by eosinophil levels as biomarker in patients with severe eosinophilic asthma without loss of asthma control 2. To evaluate if it is possible to extend the dosing interval of dupilumab, driven by FeNO as biomarker in patients with severe T2-high asthma without loss of asthma controlRead full original descriptionShow less

BIomarker-dRiven Dosing Interval Extension of biologics in asthma (the BIRDIE trial)

1. To evaluate if it is possible to extend the dosing interval of mepolizumab, driven by eosinophil levels as biomarker in patients with severe eosinophilic asthma without loss of asthma control 2. To evaluate if it is possible to extend the dosing interval of dupilumab, driven by FeNO as biomarker in patients with severe T2-high asthma without loss of asthma control

Inclusion: Severe asthma as primary indication for treatment with mepolizumab (one dose every 4 weeks) or dupilumab (one dose every 2 weeks) for the last 6 months; Stable asthma (an ACQ <1.5 and no severe asthma exacerbations) for at least 6 months; Sufficient understanding of the Dutch language.

Exclusion: Treatment with maintenance OCS, defined as treatment with OCS during 14 or more subsequent days, in the last 6 months; Treatment with immunosuppressants (other than mepolizumab, dupilumab or corticosteroids) in the last 6 months; Treatment with, or switching between, other biologics than the drug of interest in the 6 months before inclusion; Pulmonary disease(s) other than asthma (including EGPA); Pregnancy.

EU CTIS 2023-505839-12-01