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Completed Phase 2 Interventional Results available

An Evaluation of Dupilumab in Patients With Moderate to Severe Uncontrolled Asthma

ClinicalTrials.gov ID: NCT01854047

Public ClinicalTrials.gov record NCT01854047. 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 22, 2026, 4:42 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, Placebo-Controlled, Dose-Ranging Study to Evaluate Dupilumab in Patients With Moderate to Severe Uncontrolled Asthma

Brief summary

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

Primary Objective: To evaluate the efficacy of different doses and regimens of dupilumab in participants with moderate to severe uncontrolled asthma. Secondary Objective: To evaluate different doses and regimens of dupilumab in participants with moderate to severe uncontrolled asthma, with regard to: * Safety and tolerability * Dupilumab systemic exposure and anti-drug antibodies

Study identification

NCT ID
NCT01854047
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
776 participants

Conditions and interventions

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
Jun 2013 (Type not available)
Primary completion
Nov 2014 (Actual)
Completion
Apr 2015 (Actual)
Last update posted
Jun 26, 2017

2013 – 2015

United States locations

U.S. sites
50
U.S. states
24
U.S. cities
41
Facility City State ZIP Site status
Investigational Site Number 840050 Fullerton California 92835 —
Investigational Site Number 840041 Huntington Beach California 92647 —
Investigational Site Number 840019 Los Angeles California 90025 —
Investigational Site Number 840029 Los Angeles California 90025 —
Investigational Site Number 840022 Los Angeles California 90048 —
Investigational Site Number 840013 Mission Viejo California 92691 —
Investigational Site Number 840044 Newport Beach California 92663 —
Investigational Site Number 840007 Riverside California 92506 —
Investigational Site Number 840014 Rolling Hills Estates California 90274 —
Investigational Site Number 840036 San Jose California 95117 —
Investigational Site Number 840032 Colorado Springs Colorado 80907 —
Investigational Site Number 840040 Colorado Springs Colorado 80907 —
Investigational Site Number 840043 Denver Colorado 80206 —
Investigational Site Number 840006 Denver Colorado 80230 —
Investigational Site Number 840024 Denver Colorado 80230 —
Investigational Site Number 840027 Daytona Beach Florida 32117 —
Investigational Site Number 840039 Miami Florida 33135 —
Investigational Site Number 840048 Albany Georgia 31707 —
Investigational Site Number 840026 River Forest Illinois 60305 —
Investigational Site Number 840053 Evansville Indiana 47713 —
Investigational Site Number 840017 Louisville Kentucky 40223-5440 —
Investigational Site Number 840030 Owensboro Kentucky 42303 —
Investigational Site Number 840028 Baltimore Maryland 21287 —
Investigational Site Number 840052 Wheaton Maryland 20902 —
Investigational Site Number 840045 North Dartmouth Massachusetts 02747 —
Investigational Site Number 840046 Novi Michigan 48375 —
Investigational Site Number 840051 Novi Michigan 48375 —
Investigational Site Number 840018 Minneapolis Minnesota 55402 —
Investigational Site Number 840002 St Louis Missouri 63110 —
Investigational Site Number 840003 St Louis Missouri 63141 —
Investigational Site Number 840037 Missoula Montana 59804 —
Investigational Site Number 840004 Papillion Nebraska 27103 —
Investigational Site Number 840011 Princeton New Jersey 08540 —
Investigational Site Number 840016 Rochester New York 14618 —
Investigational Site Number 840025 Cincinnati Ohio 45231 —
Investigational Site Number 840015 Cincinnati Ohio 45236 —
Investigational Site Number 840020 Cincinnati Ohio 45241 —
Investigational Site Number 840001 Oklahoma City Oklahoma 73120 —
Investigational Site Number 840031 Lake Oswego Oregon 97035 —
Investigational Site Number 840034 Medford Oregon 97504 —
Investigational Site Number 840042 Philadelphia Pennsylvania 19107 —
Investigational Site Number 840010 Pittsburgh Pennsylvania 15213 —
Investigational Site Number 840009 Upland Pennsylvania 19013 —
Investigational Site Number 840021 Spartanburg South Carolina 29303 —
Investigational Site Number 840023 Dallas Texas 75231 —
Investigational Site Number 840005 El Paso Texas 79902 —
Investigational Site Number 840008 San Antonio Texas 78229 —
Investigational Site Number 840035 Richmond Virginia 23225 —
Investigational Site Number 840054 Everett Washington 98203 —
Investigational Site Number 840033 Tacoma Washington 98405 —

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 151 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01854047, 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 Jun 26, 2017 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01854047 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →