Tolerance and Efficacy Open-label Study With RV4421B, in Various Populations With Atopic Dermatitis for 12 Weeks

Recruiting now · Not applicable

Conditions studied: Atopic Dermatitis

In brief

Pierre Fabre Laboratories have developed a cream with medical device status, RV4421B-EV0407 indicated for the treatment of eczemas, including atopic eczema, contact eczema and chronic hand eczema. This product is already marketed in several countries. The objective of this clinical study is to evaluate the safety and efficacy of the study product when used alone or in association with topical corticosteroid therapy, in an ethnically diverse adult and pediatric population (including dark skin) and over a long period of time with a 12-week follow-up. 5 visits are planned: * Visit 1: Inclusion visit (Day 1) * Visit 2: Intermediate visit (Phone visit - Between Day 8 and Day 15) * Visit 3: Intermediate visit (Day 29 ± 3 days) * Visit 4: Intermediate visit (Day 57 ± 3 days) * Visit 5: End of study visit (Day 85 ± 3 days)

Key facts

Study ID: NCT07014007
Run by: Pierre Fabre Dermo Cosmetique
People needed: 105
Starts: 2025-09-30
Expected to finish: 2026-11-01
Last updated by the study team: 2026-05-05

Who can join

Age: 0 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female, with any phototype according to Fitzpatrick classification aged:
Group 1 (infants group): from 3 months to 23 months old included
Group 2 (children group): from 24 months to 12 years old included
Group 3 (teenagers \& adults group): from 13 years old
Subject with a diagnosis of atopic dermatitis according to the U.K. Working Party's Diagnostic Criteria for Atopic Dermatitis (Williams HC, Burney PG, et al.).
Subject with studied areas (lesions and prevailing xerotic areas) limited up to 30% of the body surface area
Subject with mild to moderate Atopic Dermatitis
Criteria related to treatments and/or products:
Topical corticosteroids treatments (following international treatment guidelines for each age sub-group and including investigator agreement) applied on AD lesions areas since 1 to 5 days before the inclusion and ongoing at the time of inclusion. *
The investigator will be authorized to adjust the treatment during the study.

You may not qualify if…

Criteria related to the skin condition or the disease:
Infant with Atopic Dermatitis lesions or prevailing xerotic areas located on the diaper (groups 1 \& 2)
Subject with history of allergy or intolerance to any of the study product(s) ingredients or material used for the research
Subject having any other dermatologic condition than Atopic Dermatitis, or characteristics (like tattoo…) on the studied areas liable to interfere with the study assessments
Subject having a dermatological condition, an acute, chronic or progressive disease or history of disease liable to interfere with the study data or considered by the Investigator hazardous for the subject or incompatible with the study requirements
Knowledge of Acquired Immunodeficiency Syndrome or Infectious (acute or chronic)
Criteria related to treatments and/or products:
Systemic biological immunosuppressive treatment established or modified within 12 weeks before the inclusion or planned to be started during the study
Phototherapy performed within 4 weeks before the inclusion visit or planned to be started during the study
Systemic non-biological immunosuppressive treatment established or modified within 4 weeks before the inclusion or ongoing or planned to be started during the study
Systemic corticosteroids treatment established or modified within 4 weeks before the inclusion or ongoing or planned to be started during the study
Systemic antibiotics for dermatological purposes treatment established or modified within 2 weeks before the inclusion or ongoing or planned to be started during the study
Systemic antihistaminic treatment established or modified within 2 weeks before the inclusion
Topical treatments (immunomodulators (TIMs), non-steroidal anti-inflammatory, antihistaminic, antibiotics for dermatological purposes or antiseptics) applied on studied areas within 1 week before the inclusion or ongoing or planned to be started during the study
Any other topical treatment or product applied on studied areas incompatible with the study or liable to interfere with the study assessments according to the investigator, in the weeks prior to the inclusion visit, ongoing or planned to be started during the study
Skin care product (including moisturizer) applied on the whole body between the evening before the visit and the inclusion.
Water and/or any cleansing product, applied on the whole body within 4 hours before the inclusion visit. If there is no studied area on the face, the subject is allowed to do a light face wash without time restriction (especially in the morning of the visit).
Subject who plans to modify his/her usual moisturizer (allowed outside studied areas) and/or care habits during the study
Treatment of the mother if the subject of group 1 and 2 is breastfed:
Systemic biological immunosuppressive treatment established or modified within 12 weeks before the inclusion or planned to be started during the study
Systemic non-biological immunosuppressive treatment established or modified within 4 weeks before the inclusion or planned to be started during the study
Systemic corticosteroids established or modified within 2 weeks before the inclusion or planned to be started during the study
Systemic antihistaminic established or modified within 2 weeks before the inclusion
Systemic antibiotics for dermatological purposes established or modified within 1 week before the inclusion or planned to be started during the study

Where it is running

Insight Research Ltd — Quatre Bornes, Mauritius, Mauritius (enrolling)

Full record on ClinicalTrials.gov

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