Skip to content
KStart free
AI InfrastructureDefenseQuantumAll studies →

Long-term Safety and Efficacy Evaluation of Lunsekimig in Adult Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP) Who Completed a Previous Lunsekimig CRSwNP Clinical Study

← catalyst calendar

NCT06914908 · readout in 1,624 d

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

Phase
Phase 2
Status
Enrolling by invitation
Study type
Interventional
Design
Na · None · Treatment
Enrollment
71estimated
Sites
24
Countries
Argentina, Belgium, Bulgaria +3

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
Start2025-05-12actualWhen the study began enrolling
Primary completion2031-01-29estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2031-01-29estimatedThe whole study's end, after follow-up
First posted2025-04-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-02actualThe 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 Polyps

Interventions

  • Drug: Lunsekimig — also filed as SAR443765
  • Drug: Mometasone furoate nasal spray (MFNS)

Primary outcome

what the primary-completion date above is the date OF
Incidence of participants with treatment-emergent adverse events (TEAEs) including adverse events of special interest (AESI), and serious adverse events (SAEs)
measured From baseline to Week 148

Permalink · SNY's whole pipeline · Catalyst calendar · Every registered study · What changed