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Completed Phase 4 Interventional Results available

A Study to Evaluate the Effect of Dupilumab on Exercise Capacity in Adult Patients With Asthma

ClinicalTrials.gov ID: NCT04203797

Public ClinicalTrials.gov record NCT04203797. 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 Sep 1, 2026, 7:54 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, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Effect of Dupilumab on Exercise Capacity in Patients With Moderate-to-Severe Asthma

Brief summary

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

The primary objective of the study is to demonstrate that dupilumab treatment improves exercise capacity in patients with moderate-to-severe asthma. The secondary objectives of the study are: * To demonstrate that dupilumab treatment increases physical activity of daily living in patients with moderate-to-severe asthma * To demonstrate that dupilumab treatment improves pre- and post-exercise lung function in patients with moderate-to-severe asthma

Study identification

NCT ID
NCT04203797
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
40 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 55 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 15, 2020
Primary completion
Jul 14, 2023
Completion
Jul 14, 2023
Last update posted
Apr 17, 2024

2020 – 2023

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Palos Verdes Medical Group (PVMG); Peninsula Research Associates (PRA) Rolling Hills Estates California 90274
UCLA Medical Center - Harbor Torrance California 90509
Allianz Research Institute Westminster California 92683
University of Iowa Hospitals & Clinics-Roy J. and Lucille A. Carver College of Medicine Iowa City Iowa 52242
University Of Kansas Medical Center Kansas City Kansas 66160
Infinity Medical Research North Dartmouth Massachusetts 02747
University of Michigan Ann Arbor Michigan 48109
American Health Research Charlotte North Carolina 28277
UH Cleveland Medical Center Cleveland Ohio 44106
Temple University Hospital Philadelphia Pennsylvania 19140
Regeneron Study Site Hendersonville Tennessee 37075
The University of Texas Medical School at Houston Houston Texas 77030
Intermountain Medical Center Murray Utah 84107

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04203797, 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 17, 2024 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04203797 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →