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Study details
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Efficacy of Dupilumab Added to Medium Dose Inhaled Corticosteroid/Long-acting Beta-agonist (ICS/LABA) in Comparison to ICS Dose Escalation to High Dose ICS/LABA in Adolescent and Adult Patients With Uncontrolled Asthma

Regeneron Pharmaceuticals
NCT IDNCT06572228ClinicalTrials.gov data as of Apr 2026
Phase

Phase 4

Target enrollment

250

Study length

about 2.3 years

Ages

12–80

Locations

55 sites in CA, CO, FL +20

About this study

This trial is testing whether adding dupilumab to a medium dose inhaled corticosteroid/long-acting beta-agonist (ICS/LABA) is more effective than increasing the dose of the inhaled corticosteroid/long-acting beta-agonist (ICS/LABA). It involves adults and adolescents with uncontrolled asthma who are not responding well to their current asthma medications. The goal is to determine which treatment approach provides better control of asthma symptoms.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take ICS/LABA
  • 2.Take Matching Placebo
  • 3.Take dupilumab
PhasePhase 4
Drugdupilumab

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low7%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

dupilumab

Endpoints

Secondary: Change in FEV1: FVC ratio, Change in percent predicted FEV1, Change in post-bronchodilator FEV1, Change in pre-bronchodilator FEV1, Change in pre-bronchodilator Forced expiratory volume in the first second (FEV1), Incidence of Treatment-emergent adverse event (TEAEs)

Body systems

Respiratory