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Study in Adults With Severe Chronic Rhinosinusitis With Nasal Polyposis Treated With Dupilumab in France

← catalyst calendar

NCT06393946

Sponsored by Sanofi (industry) · SNY — their whole pipeline →. With Regeneron Pharmaceuticals.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
150estimated
Sites
1
Country
France

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-10-20actualWhen the study began enrolling
Primary completion2026-07-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-07-31estimatedThe whole study's end, after follow-up
First posted2024-05-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-04actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Chronic Rhinosinusitis With Nasal Polyposis

Intervention

  • Drug: Dupilumab

Primary outcomes

what the primary-completion date above is the date OF
Patient characteristics: Age
measured At baseline (Day 1)
Patient characteristics: Sex
measured At baseline (Day 1)
Patient characteristics: Weight
measured At baseline (Day 1)
Patient characteristics: Height
measured At baseline (Day 1)
Patient characteristics: Type 2 comorbidities
measured At baseline (Day 1)
Patient characteristics: Medical history
measured At baseline (Day 1)
Patient characteristics: Lifestyle habits
measured At baseline (Day 1)
Disease characteristics: CRSwNP duration
measured At baseline (Day 1)
Disease characteristics: Age at diagnosis of CRSwNP
measured At baseline (Day 1)
Disease characteristics: Blood Eosinophils
measured At baseline (Day 1)
Disease characteristics: Total serum IgE
measured At baseline (Day 1)
Disease characteristics: Anatomopathology
measured At baseline (Day 1)
Disease characteristics: Nasal polyps score (NPS) at baseline
measured At baseline (Day 1)
Disease characteristics: Nasal congestion score (NCS) at baseline
measured At baseline (Day 1)
Disease characteristics: Rhinorrhea score (anterior/posterior) at baseline
measured At baseline (Day 1)
Disease characteristics: VAS for CRSwNP symptoms at baseline
measured At baseline (Day 1)
Disease characteristics: smell test score Visual Analog Scale (VAS) at baseline
measured At baseline (Day 1)
Concomitant and prior medications for CRSwNP or other disease: Number of patients with at least one prior or concomitant SCS
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other disease:Type of prior Systemic Corticosteroids (SCS) per patient
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other disease: Cumulative dose of SCS
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other disease: Total number of SCS bursts per patient
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other disease: Recovery of sense of smell after SCS
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other disease:Time since the most recent SCS burst before initiation of Dupixent®
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other disease: Number of prior or respiratory concomitant biotherapies per patient
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other diseases: Indication
measured From baseline up to 24 months.
Concomitant and prior medications for CRSwNP or other diseases: Reason for stop
measured From baseline up to 24 months.
Dupilumab (Dupixent®) modalities: Dosage
measured From baseline up to 24 months.
Dupilumab (Dupixent®) modalities: Injection modalities
measured From baseline up to 24 months.
Dupilumab (Dupixent®) modalities: Treatment duration
measured From baseline up to 24 months.
Dupilumab (Dupixent®) modalities: Compliance with treatment
measured From baseline up to 24 months.

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