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Completed Phase 3 Interventional Results available

Controlled Clinical Study of Dupilumab in Patients With Nasal Polyps

ClinicalTrials.gov ID: NCT02898454

Public ClinicalTrials.gov record NCT02898454. 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 Jul 22, 2026, 1:44 AM 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, Double-blind, 52-week, Placebo Controlled Efficacy and Safety Study of Dupilumab, in Patients With Bilateral Nasal Polyposis on a Background Therapy With Intranasal Corticosteroids

Study identification

NCT ID
NCT02898454
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
448 participants

Conditions and interventions

Interventions

  • Dupilumab SAR231893 (REGN668) Drug
  • Placebo Drug
  • Mometasone furoate nasal spray Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Nov 27, 2016
Primary completion
Aug 26, 2018
Completion
Nov 15, 2018
Last update posted
Oct 22, 2019

2016 – 2018

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Investigational Site Number 8400019 Birmingham Alabama 35209
Investigational Site Number 8400011 Fresno California 93720
Investigational Site Number 8400008 Huntington Beach California 92647
Investigational Site Number 8400004 Rolling Hills Estates California 90274
Investigational Site Number 8400012 Walnut Creek California 94598
Investigational Site Number 8400017 Colorado Springs Colorado 80909
Investigational Site Number 8400006 Denver Colorado 80230
Investigational Site Number 8400022 New Haven Connecticut 06519
Investigational Site Number 8400002 Louisville Kentucky 40207
Investigational Site Number 8400021 Boston Massachusetts 02114
Investigational Site Number 8400014 Kansas City Missouri 64114
Investigational Site Number 8400024 The Bronx New York 10461
Investigational Site Number 8400016 North Charleston North Carolina 29420
Investigational Site Number 8400013 Bethlehem Pennsylvania 18017
Investigational Site Number 8400005 Philadelphia Pennsylvania 19104
Investigational Site Number 8400003 Pittsburgh Pennsylvania 15213
Investigational Site Number 8400009 Salt Lake City Utah 84132
Investigational Site Number 8400010 Bellevue Washington 98225
Investigational Site Number 8400007 Milwaukee Wisconsin 53219

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 104 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02898454, 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 Oct 22, 2019 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02898454 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →