Newnan, Georgia 30263

  • Prurigo Nodularis

Purpose:

The primary objective is to assess the efficacy of nemolizumab (CD14152) compared to placebo in participants greater than or equal to (>=) 18 years of age with prurigo nodularis (PN) after a 16 week treatment period.


Criteria:

Inclusion Criteria: - Clinical diagnosis of PN for at least 6 months with: (a) Pruriginous nodular lesions on upper limbs, trunk, and/or lower limbs; (b) At least 20 nodules on the entire body with a bilateral distribution; (c) Investigator Global Assessment (IGA) score >= 3 (based on the IGA scale ranging from 0 to 4, in which 3 is moderate and 4 is severe) at both the screening and baseline visits - Severe pruritus defined as follows on the PP NRS: (a) at the screening visit (Visit 1): PP NRS score is >= 7.0 for the 24-hour period immediately preceding the screening visit; (b) at the baseline visit (Visit 2): Mean of the daily intensity of the PP NRS score is >= 7.0 over the previous week - Female participants of childbearing potential (that is [i.e,], fertile, following menarche and until becoming post-menopausal unless permanently sterile) must agree to use at least 1 effective and approved method of contraception throughout the study and for 12 weeks after the last study drug injection - Participant is willing and able to comply with all of the time commitments and procedural requirements of the clinical study protocol, including daily diary recordings by the participant using an electronic handheld device provided for this study Exclusion Criteria: - Body weight < 30 kilogram (kg) - Unilateral lesions of prurigo (eg, only one arm affected) - History of or current confounding skin condition (eg, Netherton syndrome, cutaneous T-cell lymphoma [mycosis fungoides or Sezary syndrome], chronic actinic dermatitis, dermatitis herpetiformis) - Participants with a current medical history of chronic obstructive pulmonary disease and/or chronic bronchitis - Positive serology results (hepatitis B surface antigen [HBsAg] or hepatitis B core antibody [HBcAb], hepatitis C (HCV) antibody with positive confirmatory test for HCV (eg, polymerase chain reaction [PCR]), or human immunodeficiency virus antibody) at the screening visit


NCT ID:

NCT04501666


Primary Contact:

Galderma Research & Development
Phone: 817-961-5000
Email: clinical.studies@galderma.com


Backup Contact:

N/A


Location Contact:

Newnan, Georgia 30263
United States

Galderma Investigational Site
Phone: 770-252-6900

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: September 27, 2021

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