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Clinical Trials in the EU / 2025-521620-29-01
Completed Phase II

Efficacy and safety of two moisturising creams for maintenance treatment of atopic dermatitis compared to no treatment: A prospective, controlled, split-body study

2025-521620-29-01 · tracked via the Priya Life Science EU tracker
Sponsor
Galenica AB
Sponsor type
Pharmaceutical company
Therapeutic area
Skin and Connective Tissue Diseases
Decision date
24/11/2025
Enrollment target
78
Sites
Norway, Sweden

Condition studied

Atopic Dermatitis

Investigational medicinal product(s)

Urea/propylene glycol 50 mg/g + 250 mg/g creamOviderm 250 mg/g kräm

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

• Time to relapse of eczema (patient reported outcome [PRO]) on a defined study area from baseline until the eczema relapses or until the end of the maintenance phase, whichever comes first

Endpoint detail

• Time to relapse of eczema (PRO) on a defined study area from baseline until the eczema relapses or until the end of the maintenance phase, whichever comes first, • Change in self-reported pruritus on defined study area from baseline until the eczema relapses or until the end of the maintenance phase, whichever comes first, using Peak Pruritus Numerical Rating Scale (NRS), • Change in self-reported pruritus on defined study area from baseline until the eczema relapses or until the end of the maintenance phase, whichever comes first, using Peak Pruritus Numerical Rating Scale (NRS) per time, • Frequency of adverse events during the maintenance phase

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-521620-29-01 on CTIS ↗ ← All trials in the EU