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Completed Phase 3 Interventional Results available

A Study to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Participants With Prurigo Nodularis (PN)

ClinicalTrials.gov ID: NCT04501679

Public ClinicalTrials.gov record NCT04501679. 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, 11:04 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 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Subjects With Prurigo Nodularis

Study identification

NCT ID
NCT04501679
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Galderma R&D
Industry
Enrollment
274 participants

Conditions and interventions

Interventions

  • Nemolizumab Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 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
Aug 10, 2020
Primary completion
Mar 29, 2022
Completion
Mar 30, 2022
Last update posted
Jul 9, 2024

2020 – 2022

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Galderma Investigational Site Fountain Valley California 92708
Galderma Investigational Site San Diego California 92123
Galderma Investigational Site Washington D.C. District of Columbia 20037
Galderma Investigational Site Aventura Florida 33180
Galderma Investigational Site Miami Florida 33136
Galderma Investigational Site North Miami Beach Florida 33162-4708
Galderma Investigational Site Ormond Beach Florida 32174
Galderma Investigational Site Chicago Illinois 60602
Galderma Investigational Site Indianapolis Indiana 46250
Galderma Investigational Site Louisville Kentucky 40241
Galderma Investigational Site Boston Massachusetts 02111
Galderma Investigational Site Saint Joseph Michigan 49085
Galderma Investigational Site New York New York 10021
Galderma Investigational Site Cincinnati Ohio 45627
Galderma Investigational Site Dublin Ohio 43016
Galderma Investigational Site Anderson South Carolina 29621
Galderma Investigational Site Murfreesboro Tennessee 37130
Galderma Investigational Site Dallas Texas 75230
Galderma Investigational Site Dripping Springs Texas 78620
Galderma Investigational Site Pflugerville Texas 78660
Galderma Investigational Site Webster Texas 77004
Galderma Investigational Site Morgantown West Virginia 26505

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 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04501679, 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 Jul 9, 2024 · 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 NCT04501679 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →