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Terminated Phase 2 Interventional Results available

Efficacy, Safety, and Pharmacokinetic Profiles of REGN3500 Administered to Adult Patients With Moderate-to-Severe Atopic Dermatitis

ClinicalTrials.gov ID: NCT03738423

Public ClinicalTrials.gov record NCT03738423. 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 2, 2026, 5:19 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 Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging Study Investigating the Efficacy, Safety, and Pharmacokinetic Profiles of REGN3500 Administered to Adult Patients With Moderate-to- Severe Atopic Dermatitis

Brief summary

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

The primary objective of the study is to assess the efficacy of REGN3500 monotherapy in Atopic dermatitis (AD), as well as understand the dose-response relationship, compared with placebo treatment, in adult patients with moderate-to-severe AD. Secondary objectives are to: * Assess the safety and tolerability of subcutaneous (SC) doses of REGN3500 monotherapy in adult patients with moderate-to-severe AD * Assess the Pharmacokinetics (PK) of REGN3500 in adult patients with moderate-to-severe AD * Assess the immunogenicity of REGN3500 in adult patients with moderate-to-severe AD

Study identification

NCT ID
NCT03738423
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
129 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Nov 12, 2018
Primary completion
Mar 12, 2020
Completion
Jul 23, 2020
Last update posted
Jun 9, 2022

2018 – 2020

United States locations

U.S. sites
31
U.S. states
21
U.S. cities
27
Facility City State ZIP Site status
Regeneron Study Site Birmingham Alabama 35209
Regeneron Study Site Phoenix Arizona 85006
Regeneron Study Site Scottsdale Arizona 85259
Regeneron Study Site Tucson Arizona 85718
Regeneron Study Site Little Rock Arkansas 72205
Regeneron Study Site Fountain Valley California 92708
Regeneron Study Site Fremont California 94538
Regeneron Study Site Oceanside California 92056
Regeneron Study Site Sacramento California 95815
Regeneron Study Site Santa Monica California 90404
Regeneron Study Site Jacksonville Florida 32256
Regeneron Study Site Macon Georgia 31217
Regeneron Study Site Skokie Illinois 60077
Regeneron Study Site Evansville Indiana 47714
Regeneron Study Site Overland Park Kansas 66215
Regeneron Study Site Louisville Kentucky 40202
Regeneron Study Site Louisville Kentucky 40217
Regeneron Study Site Louisville Kentucky 40241
Regeneron Study Site Saint Joseph Michigan 49085
Regeneron Study Site Minneapolis Minnesota 55402
Regeneron Study Site Las Vegas Nevada 89148
Regeneron Study Site Lebanon New Hampshire 03756
Regeneron Study Site New York New York 10022
Regeneron Study Site Wilmington North Carolina 28405
Regeneron Study Site Cincinnati Ohio 45231
Regeneron Study Site Norman Oklahoma 73071
Regeneron Study Site North Charleston South Carolina 29420
Regeneron Study Site San Antonio Texas 78218
Regeneron Study Site San Antonio Texas 78229
Regeneron Study Site San Antonio Texas 78258
Regeneron Study Site Norfolk Virginia 23502

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 58 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03738423, 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 9, 2022 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03738423 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →