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Real-world Experience on Using Nemolizumab in the Treatment of Moderate-to- Severe Prurigo Nodularis in Adults

RecruitingObservational study

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Participants who, according to the treating physician's decision and in line with the local package label, are newly initiated on nemolizumab (Nemluvio®) for the treatment of PN.
* Participants greater than or equal to (\>=) 18 years of age.
* Participants who signed the written informed consent form (ICF).

Exclusion Criteria:

* Have contraindication(s) for the use of nemolizumab (Nemluvio®) according to the local package label;
* Participants who received treatment with a drug under clinical development/ investigation within 3 months prior to baseline.
* Participants who received nemolizumab previously.
* Participants who are mentally, physically, or linguistically unable to understand the content of the ICF and/or to complete the study questionnaires.

About the study

The main aim of this study is to assess real-world effectiveness of nemolizumab in Prurigo nodularis (PN) as measured by investigator and patient reported outcome (PRO) in clinical practice at Month 6.

Sponsor: Galderma R&D · Participants: 600 · Started: Aug 11, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06988618

Locations in the U.S.

AlabamaGalderma Investigational Site # 8893, Birmingham
ArizonaGalderma Investigational Site # 7060, Phoenix
Galderma Investigational Site # 7077, Phoenix
Galderma Investigational Site # 7067, Tucson
CaliforniaGalderma Investigational Site # 7074, Corona
Galderma Investigational Site # 6836, Fountain Valley
Galderma Investigational Site # 8224, Fremont
Galderma Investigational Site # 7064, Santa Monica
ColoradoGalderma Investigational Site # 7061, Castle Rock
ConnecticutGalderma Investigational Site # 7059, Fairfield
FloridaGalderma Investigational Site # 7087, Coral Gables
Galderma Investigational Site # 7063, Cutler Bay
Galderma Investigational Site # 7078, Miami
Galderma Investigational Site # 7070, North Miami Beach
Galderma Investigational Site # 7091, Tampa
IllinoisGalderma Investigational Site # 7058, Chicago (Not yet recruiting)
IndianaGalderma Investigational Site # 8142, Indianapolis
MarylandGalderma Investigational Site # 8012, Glendale
Galderma Investigational Site # 7068, Rockville
MassachusettsGalderma Investigational Site # 7065, Brighton
MichiganGalderma Investigational Site # 7066, Auburn Hills
Galderma Investigational Site # 7071, Caledonia
Galderma Investigational Site # 7072, Troy
Galderma Investigational Site # 7053, Waterford
MissouriGalderma Investigational Site # 7057, Lee's Summit
Galderma Investigational Site # 7076, St Louis
New HampshireGalderma Investigational Site # 7055, Portsmouth
New YorkGalderma Investigational Site # 7080, Auburn
Galderma Investigational Site # 7052, East Syracuse
Galderma Investigational Site # 8282, Mount Kisco
Galderma Investigational Site # 7051, New York
Galderma Investigational Site # 7056, New York
OhioGalderma Investigational Site # 7081, Dayton
PennsylvaniaGalderma Investigational Site # 8559, Philadelphia
TexasGalderma Investigational Site # 8238, Dallas
Galderma Investigational Site # 7062, Edinburg
Galderma Investigational Site # 7088, Grapevine
Galderma Investigational Site # 7069, Sugar Land
VirginiaGalderma Investigational Site # 7079, Vienna

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.