Severe asthma
Conditions
Brief summary
The main study endpoint is the number of injections in the mepolizumab and in the dupilumab intervention group compared to the control groups during the follow-up period.
Interventions
DRUGDupixent 100 mg solution for injection in pre-filled syringe
Sponsors
Sint Franciscus Vlietland Groep Stichting
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study endpoint is the number of injections in the mepolizumab and in the dupilumab intervention group compared to the control groups during the follow-up period. | — |
Countries
Netherlands
Outcome results
None listed