WHO ICTRP trial

A study to assess the efficacy and safety of nemolizumab (CD14152) in subjects…

EUCTR2019-004789-17-FR · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2019-004789-17-FR
Public title A study to assess the efficacy and safety of nemolizumab (CD14152) in subjects with prurigo nodularis (PN)
Scientific title A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Subjects with Prurigo Nodularis - A study to assess the efficacy and safety of nemolizumab in subjects with prurigo nodularis
Primary sponsor Galderma S.A.
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no
Countries United States;France;Canada;Poland;Belgium;Spain;Netherlands;Switzerland
Conditions Prurigo Nodularis MedDRA version: 20.0 Level: LLT Classification code 10037084 Term: Prurigo nodularis System Organ Class: 100000004858 ;Therapeutic area: Diseases [C] - Skin and Connective Tissue Diseases [C17]
Interventions Product Name: CD14152 Product Code: CD14152 Pharmaceutical Form: Powder and solution for solution for injection INN or Proposed INN: NEMOLIZUMAB CAS Number: 1476039-58-3 Current Sponsor code: CD14152 / CIM331 Other descriptive name…
Registration date Apr 15, 2020
Target size 240
Secondary IDs RD.06.SPR.203065;117122
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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