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Completed Phase 3 Interventional Results available

Efficacy & Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis

ClinicalTrials.gov ID: NCT03989349

Public ClinicalTrials.gov record NCT03989349. 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 17, 2026, 9:10 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 Study to Assess the Efficacy and Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis

Brief summary

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

The main purpose of the study was to assess the efficacy and safety of nemolizumab after a 16-week treatment period in adult and adolescent subjects with moderate-to-severe atopic dermatitis (AD) not adequately controlled with topical treatments.

Study identification

NCT ID
NCT03989349
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Galderma R&D
Industry
Enrollment
787 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 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 30, 2019 (Actual)
Primary completion
Feb 23, 2022 (Actual)
Completion
Sep 26, 2022 (Actual)
Last update posted
Aug 14, 2024

2019 – 2022

United States locations

U.S. sites
47
U.S. states
21
U.S. cities
41
Facility City State ZIP Site status
Galderma Investigational Site 8749 Birmingham Alabama 35244 —
Galderma Investigational Site 8893 Birmingham Alabama 35244 —
Galderma Investigational Site 8866 Guntersville Alabama 35976 —
Galderma Investigational Site 8808 Scottsdale Arizona 85255 —
Galderma Investigational Site 8906 Bell Gardens California 90201 —
Galderma Investigational Site 8905 Canoga Park California 91304 —
Galderma Investigational Site 8577 Encinitas California 92024 —
Galderma Investigational Site 8673 Garden Grove California 92840 —
Galderma Investigational Site 8683 Los Angeles California 90033 —
Galderma Investigational Site 8907 Newport Beach California 92660 —
Galderma Investigational Site 8799 Ontario California 91762 —
Galderma Investigational Site 8745 Pasadena California 91105 —
Galderma Investigational Site 8658 San Diego California 92123 —
Galderma Investigational Site 8536 Santa Ana California 92705 —
Galderma Investigational Site 8820 Westminster California 92683 —
Galderma Investigational Site 8637 Farmington Connecticut 06030 —
Galderma Investigational Site 8875 Delray Beach Florida 33484 —
Galderma Investigational Site 8391 Hialeah Florida 33013 —
Galderma Investigational Site 8727 Hialeah Florida 33016 —
Galderma Investigational Site 8523 Largo Florida 33770 —
Galderma Investigational Site 8719 Miami Florida 33125 —
Galderma Investigational Site 8656 Miami Florida 33137 —
Galderma Investigational Site 8704 Miami Florida 33155 —
Galderma Investigational Site 8706 Miami Florida 33175 —
Galderma Investigational Site 8203 Tampa Florida 33607 —
Galderma Investigational Site 8839 Tampa Florida 33615 —
Galderma Investigational Site 8729 Rolling Meadows Illinois 60008 —
Galderma Investigational Site 8724 New Albany Indiana 47150 —
Galderma Investigational Site 8554 Detroit Michigan 48202 —
Galderma Investigational Site 8825 Las Vegas Nevada 89106 —
Galderma Investigational Site 8506 Hackensack New Jersey 07601 —
Galderma Investigational Site 8741 Buffalo New York 14221 —
Galderma Investigational Site 8723 Cortland New York 13045 —
Galderma Investigational Site 8733 New York New York 10022 —
Galderma Investigational Site 8823 Greensboro North Carolina 27408 —
Galderma Investigational Site 8030 Raleigh North Carolina 27612 —
Galderma Investigational Site 8747 Cincinnati Ohio 45219 —
Galderma Investigational Site 8212 Portland Oregon 97210 —
Galderma Investigational Site 8721 Pittsburgh Pennsylvania 15213 —
Galderma Investigational Site 8713 North Charleston South Carolina 29420 —
Galderma Investigational Site 8705 Chattanooga Tennessee 37421 —
Galderma Investigational Site 8807 Houston Texas 77029 —
Galderma Investigational Site 8618 Waco Texas 76710 —
Galderma Investigational Site 8003 Webster Texas 77598 —
Galderma Investigational Site 8672 Salt Lake City Utah 84117 —
Galderma Investigational Site 8896 Richmond Virginia 23219 —
Galderma Investigational Site 8434 Seattle Washington 98105 —

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 91 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03989349, 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 Aug 14, 2024 · Synced Oct 17, 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 public registry record, listed eligibility criteria, and available contact information for NCT03989349 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →