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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT03985943

Public ClinicalTrials.gov record NCT03985943. 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, 2:50 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
NCT03985943
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Galderma R&D
Industry
Enrollment
941 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 26, 2019
Primary completion
Dec 28, 2021
Completion
Aug 10, 2022
Last update posted
Aug 13, 2024

2019 – 2022

United States locations

U.S. sites
57
U.S. states
23
U.S. cities
51
Facility City State ZIP Site status
Galderma Investigational Site 8880 North Little Rock Arkansas 72117
Galderma Investigational Site 8578 Cerritos California 90703
Galderma Investigational Site 8636 Fountain Valley California 92708
Galderma Investigational Site 8888 Fullerton California 92835
Galderma Investigational Site 8686 Lomita California 90717
Galderma Investigational Site 8674 Los Angeles California 90025
Galderma Investigational Site 8125 San Francisco California 94115
Galderma Investigational Site 8895 Santa Ana California 92703
Galderma Investigational Site 8608 Santa Monica California 90404
Galderma Investigational Site 8897 Brandon Florida 33511
Galderma Investigational Site 8805 Cape Coral Florida 33991
Galderma Investigational Site 8902 Doral Florida 33122
Galderma Investigational Site 8804 Hialeah Florida 33016
Galderma Investigational Site 8711 Jacksonville Florida 32256
Galderma Investigational Site 8710 Miami Florida 33126
Galderma Investigational Site 8801 Miami Florida 33145
Galderma Investigational Site 8737 Miami Florida 33174
Galderma Investigational Site 8708 Miami Florida 33176
Galderma Investigational Site 8806 Miami Lakes Florida 33014
Galderma Investigational Site 8800 Miami Lakes Florida 33016
Galderma Investigational Site 8734 Pembroke Pines Florida 33028
Galderma Investigational Site 8744 Macon Georgia 31217
Galderma Investigational Site 8728 Newnan Georgia 30263
Galderma Investigational Site 8887 Union City Georgia 30291
Galderma Investigational Site 8890 Blackfoot Idaho 83221
Galderma Investigational Site 8819 Nampa Idaho 83687
Galderma Investigational Site 8571 Skokie Illinois 60076
Galderma Investigational Site 8712 Skokie Illinois 60077
Galderma Investigational Site 8142 Indianapolis Indiana 46250
Galderma Investigational Site 8771 Louisville Kentucky 40241
Galderma Investigational Site 8882 Bangor Maine 04401
Galderma Investigational Site 8743 Ann Arbor Michigan 48109
Galderma Investigational Site 8512 Bay City Michigan 48706
Galderma Investigational Site 8155 Troy Michigan 48084
Galderma Investigational Site 8748 Ypsilanti Michigan 48197
Galderma Investigational Site 8521 Saint Joseph Missouri 64506
Galderma Investigational Site 8718 Missoula Montana 59808
Galderma Investigational Site 8810 Omaha Nebraska 68144
Galderma Investigational Site 8740 Henderson Nevada 89052
Galderma Investigational Site 8242 Brooklyn New York 11203
Galderma Investigational Site 8620 New York New York 10023
Galderma Investigational Site 8279 New York New York 10075
Galderma Investigational Site 8648 Wilmington North Carolina 28405
Galderma Investigational Site 8702 Bexley Ohio 43209
Galderma Investigational Site 8595 Dublin Ohio 43016
Galderma Investigational Site 8206 Norman Oklahoma 73071
Galderma Investigational Site 8857 Oklahoma City Oklahoma 73118
Galderma Investigational Site 8255 Philadelphia Pennsylvania 19103
Galderma Investigational Site 8802 Plymouth Meeting Pennsylvania 19462
Galderma Investigational Site 8736 Charleston South Carolina 29425
Galderma Investigational Site 8818 Rapid City South Dakota 57702
Galderma Investigational Site 8133 Arlington Texas 76011
Galderma Investigational Site 8238 Dallas Texas 75230
Galderma Investigational Site 8827 Dripping Springs Texas 78620
Galderma Investigational Site 8664 Frisco Texas 75034
Galderma Investigational Site 8042 Houston Texas 77056
Galderma Investigational Site 8862 Fairfax Virginia 22031

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 117 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03985943, 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 13, 2024 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03985943 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →