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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

⁃ Criteria related to the population:

⁃ \- Subject aged between 18 and 75 years included.

⁃ Criteria related to the disease:

• Subject with facial vitiligo, regardless of its duration.

• having a sufficient repigmentation rate of the vitiligo after repigmenting treatment

⁃ Criteria related to treatments and/or products:

⁃ \- Subject responder to a repigmenting treatment

Locations
Other Locations
France
COSDERMA
RECRUITING
Bordeaux
Contact Information
Primary
Christophe CHAMARD
christophe.chamard@pierre-fabre.com
+335.34.50.65.88
Backup
Adeline BACQUEY
adeline.bacquey@pierre-fabre.com
+335.34.50.65.33
Time Frame
Start Date: 2024-05-23
Estimated Completion Date: 2025-06-01
Participants
Target number of participants: 50
Treatments
Treated group
Control group
Related Therapeutic Areas
Sponsors
Leads: Pierre Fabre Dermo Cosmetique

This content was sourced from clinicaltrials.gov