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Completed Phase 2Phase 3 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Dupilumab in Adult Patients With Bullous Pemphigoid

ClinicalTrials.gov ID: NCT04206553

Public ClinicalTrials.gov record NCT04206553. 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, 6:51 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Dupilumab in Adult Patients With Bullous Pemphigoid

Study identification

NCT ID
NCT04206553
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
106 participants

Conditions and interventions

Interventions

  • dupilumab Drug
  • Matching Placebo Drug
  • Oral corticosteroids (OCS) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 90 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
Oct 27, 2020
Primary completion
Jul 11, 2024
Completion
Jan 4, 2025
Last update posted
Jun 17, 2026

2020 – 2025

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
Regeneron study Site Birmingham Alabama 35233
Regeneron Study Site Scottsdale Arizona 85259
Regeneron Study Site Redwood City California 94063
Regeneron Study Site Farmington Connecticut 06030
Regeneron Study Site Miami Florida 33125
Regeneron study Site Orlando Florida 32827
Regeneron Study Site Iowa City Iowa 52242
Regeneron Study Site Boston Massachusetts 02116
Regeneron study Site Ann Arbor Michigan 48109-5314
Regeneron Study Site Chapel Hill North Carolina 27516
Regeneron Study Site Portland Oregon 97239
Regeneron Study Site Philadelphia Pennsylvania 19104
Regeneron study Site Providence Rhode Island 02908
Regeneron Study Site Murray Utah 84107
Regeneron study Site Charlottesville Virginia 22903

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 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04206553, 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 17, 2026 · 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 NCT04206553 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →