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Study Assessing Long-teRm Outcomes of dupiluMAb (DUPIXENT®) Treatment in Adult Patients With Chronic Rhinosinusitis With Nasal Polyposis (CRSwNP)
NCT04959448 · View on ClinicalTrials.gov ↗
Study Summary
The primary objectives of the study are: * To longitudinally characterize the long-term effectiveness of DUPIXENT® through assessment of patient-reported symptoms, Health-Related Quality of Life (HRQoL) related to Chronic rhinosinusitis with nasal polyposis (CRSwNP) and other type 2 comorbidities, and their change over-time. * To characterize patients who receive DUPIXENT® for CRSwNP in a real-world setting with respect to their medical history, demographic and disease characteristics, and type 2 comorbidities The secondary objectives of the study are: * To characterize real-world utilization of DUPIXENT® for patients with CRSwNP * To collect patient and physician global assessment of disease severity and treatment satisfaction for patients receiving DUPIXENT® for CRSwNP * To collect long-term safety data for patients receiving DUPIXENT® for CRSwNP
Conditions Studied
Interventions
- DRUG DUPIXENT®
Study Locations (20)
California
- The Allergy and Rheumatology Medical Clinic — La Jolla
- ARK Clinical Research — Long Beach
- Scripps Health - Scripps Clinic Carmel Valley — San Diego
- Breathe Clear Institute — Torrance
- Allergy & Asthma Clinical Research — Walnut Creek
Florida
- AADRS Clincial Research Center — Coral Gables
- University of Florida — Gainesville
- Damask Physicians Group — Lake Mary
- University of South Florida — Tampa
Illinois
- Northwestern University Feinberg School of Medicine — Chicago
- University of Illinois — Chicago
- The University of Chicago Medical Center UCMC Duchossois Center for Advanced Medicine DCAM — Chicago
- Asthma & Allergy Center of Chicago — Oak Park
Georgia
- Emory University Hospital Midtown — Atlanta
- IACT Health — Columbus
Alabama
- Excel ENT of Alabama — Birmingham
Arizona
- Medical Research of Arizona, a division of Allergy, Asthma & Immunology Associates — Scottsdale
Idaho
- Treasure Valley Medical Research — Boise
Indiana
- Indiana University Health — Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 717 participants |
| Start Date | 2021-08-12 |
| Est. Completion | 2027-03-25 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04959448
The ClinicalTrials.gov registry entry for NCT04959448 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 717 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Regeneron Pharmaceuticals, which has 290 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Chronic Rhinosinusitis With Nasal Polyposis appearing as the primary indexed condition, and to 1 intervention — of which DUPIXENT® is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04959448 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Florida, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04959448 about?
NCT04959448 is a clinical study titled "Study Assessing Long-teRm Outcomes of dupiluMAb (DUPIXENT®) Treatment in Adult Patients With Chronic Rhinosinusitis With Nasal Polyposis (CRSwNP)". The primary objectives of the study are: * To longitudinally characterize the long-term effectiveness of DUPIXENT® through assessment of patient-reported symptoms, Health-Related Quality of Life (HRQoL) related to Chronic rhinosinusitis with nasal polyposis (CRSwNP) and other type 2 comorbidities, ...
What is the current status of trial NCT04959448?
This trial is currently active not recruiting. The enrollment target is 717 participants. The study started on 2021-08-12. Estimated completion is 2027-03-25.
What conditions does trial NCT04959448 study?
This clinical trial studies the following conditions: Chronic Rhinosinusitis With Nasal Polyposis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04959448?
The interventions under investigation include: DUPIXENT® (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04959448?
This trial is sponsored by Regeneron Pharmaceuticals, which has 290 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04959448 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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