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Completed Phase 2 Interventional

A Proof-of-concept Study of Lunsekimig Compared With Placebo in Adults With Chronic Rhinosinusitis With Nasal Polyps

ClinicalTrials.gov ID: NCT06454240

Public ClinicalTrials.gov record NCT06454240. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 4:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized Phase 2, Double-blind, Placebo-controlled, Parallel-group, 2-arm Study to Assess the Efficacy, Safety, and Tolerability of Subcutaneous Lunsekimig in Adult Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a parallel, Phase 2, 2-arm, multicenter, randomized, double-blind, placebo-controlled, proof-of-concept study for treatment of CRSwNP. The purpose of this study is to assess the efficacy, safety, and tolerability of add-on therapy with subcutaneous lunsekimig in adult participants (aged 18 to 70 years, inclusive) with CRSwNP who are inadequately controlled on intranasal corticosteroid treatment. Participants with and without co-morbid asthma will be included in the study, and lung function will be assessed in both groups. The study duration will be up to approximately 40 weeks per participant, including 4 weeks of screening run-in period, 24 weeks of intervention period, and 12 weeks of follow-up.

Study identification

NCT ID
NCT06454240
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
79 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 17, 2024 (Actual)
Primary completion
Jan 29, 2026 (Actual)
Completion
Apr 23, 2026 (Actual)
Last update posted
Apr 28, 2026

2024 – 2026

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
Allergy & Rheumatology- Site Number : 8400005 La Jolla California 92037 —
Sacramento Ear Nose & Throat - Roseville- Site Number : 8400003 Roseville California 95661 —
Senta Clinic- Site Number : 8400025 San Diego California 92018 —
James A Haley Veterans' Hospital- Site Number : 8400015 Tampa Florida 33612 —
Emory University Hospital Midtown- Site Number : 8400012 Atlanta Georgia 30308 —
The Allergy Group - Asthma & Allergy Boise- Site Number : 8400002 Boise Idaho 83706 —
Harvard Medical School - Brigham and Women's Hospital Site Number : 8400016 Boston Massachusetts 02115 —
Essential Medical Research- Site Number : 8400020 Tulsa Oklahoma 74137 —
McGovern Medical School - UT Physicians Dermatology - Bellaire Station- Site Number : 8400017 Bellaire Texas 77401 —
Gary Gross Pharmaceutical Research & Consulting, Inc. Site Number : 8400004 Dallas Texas 75231 —
Berkson Medical - McKinney- Site Number : 8400014 McKinney Texas 75070 —
Alamo ENT Associates Site Number : 8400001 San Antonio Texas 78258 —
Advanced Research Institute - Odgen- Site Number : 8400022 Ogden Utah 84405 —
Eastern Virginia Medical School (EVMS) Medical Group- Site Number : 8400008 Norfolk Virginia 23510 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06454240, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 28, 2026 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06454240 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →