BENITIONSClinical Trial Intelligence

Dupilumab in CRSsNP

Phase 2 Completed NCT04678856

ConditionChronic Rhinosinusitis Without Nasal Polyps, Sinusitis, Chronic Sinusitis, Sinus Disorder
PhasePhase 2
SponsorSanofi
StatusCompleted
Enrollment71 participants
InterventionsDupilumab SAR231893
Start dateDec 2, 2020
Completion dateNov 14, 2023
Results postedDec 18, 2024

Summary

Primary Objective: To evaluate the efficacy of dupilumab as assessed by the reduction at Week 24 in sinus opacification on computerized tomography (CT) scan in the dupilumab group only Secondary Objectives: * To evaluate the efficacy of dupilumab as assessed by the reduction at Week 24 in sinus opacification on CT scan and sinus total symptom score (sTSS) compared to placebo * To evaluate the safety and tolerability of dupilumab in CRSsNP patients compared to placebo * To evaluate the pharmacokinetics (PK) of dupilumab in CRSsNP patients compared to placebo * Assessment of immunogenicity to dupilumab over time compared to placebo

Change From Baseline to Week 24 in Opacification of Sinuses Assessed by Computed Tomography (CT) Scan Using the Lund Mackay (LMK) Score in Dupilumab Group

Baseline (Day 1) and Week 24 · Score on a scale

Dupilumab 300 mg q2w-6.63 ± 3.91 Score on a scale

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