Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06446063

Efficacy & Tolerance of Cosmetic Product RV5098A on Face Pigmentation Maintenance in Adult Vitiligo Patients.

Efficacy and Tolerance of the Cosmetic Care Product RV5098A on the Maintenance of Pigmentation on Face in Adult Patients With Vitiligo.

Status
Recruiting
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Pierre Fabre Dermo Cosmetique · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Vitiligo is an autoimmune depigmentation disorder affecting 0.5 to 1% of the population worldwide. Vitiligo lesions are characterized by a progressive loss of pigmentation caused by the disappearance of functioning melanocytes in the epidermis, mainly resulting from the activation of immune cells in a genetically predisposed patient. Despite major advances in the understanding of the mechanisms of the disease, the treatment remains challenging. Different treatment strategies could lead to cosmetically acceptable repigmentation (\>75%), particularly on face and neck. However, after repigmentation, the risk of relapse is estimated at nearly 40% during the first year after stopping treatment. To date, long-term management remains a challenge. With their topical product RV5098A adapted for patients with vitiligo, Pierre Fabre Laboratories hypothesize that it could be effective in maintaining pigmentation of previously repigmented lesions in adults with facial vitiligo.

Conditions

Interventions

TypeNameDescription
OTHERTest productTwice daily applications The product is applied to the entire face.
OTHERControl ProductTwice daily applications The product is applied to the entire face.

Timeline

Start date
2024-05-23
Primary completion
2025-06-01
Completion
2025-06-01
First posted
2024-06-06
Last updated
2024-06-06

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06446063. Inclusion in this directory is not an endorsement.