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

Last updated: May 31, 2024
Sponsor: Pierre Fabre Dermo Cosmetique
Overall Status: Active - Recruiting

Phase

N/A

Condition

Vitiligo

Treatment

Test product

Control Product

Clinical Study ID

NCT06446063
RV5098A20230158
  • Ages 18-75
  • All Genders

Study 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 Criteria

Inclusion

Inclusion Criteria:

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

Non-inclusion Criteria:

Criteria related to the diseases / skin condition:

  • Subject with active vitiligo.

  • Subject with spontaneous repigmentation without treatment.

  • Subject having other dermatological condition, an acute, chronic, or progressive disease or history of disease liable to interfere with the study assessments or considered by the Investigator hazardous for the subject or incompatible with the study requirements.

Criteria related to treatments and/or products:

  • Systemic immunomodulatory treatment taken for another pathology, before inclusion, on-going or planned to be established during the study.

  • Any topical immunomodulatory treatment applied on the face for another pathology, on-going or planned to be established during the study.

  • Any other topical or systemic treatment established or modified during the previous weeks or planned to be established or modified during the study, liable to interfere with the evaluation of the efficacy according to the investigator's assessment.

  • Any dietary supplement for vitiligo within 4 weeks before the inclusion visit or planned to be established during the study.

Study Design

Total Participants: 50
Treatment Group(s): 2
Primary Treatment: Test product
Phase:
Study Start date:
May 23, 2024
Estimated Completion Date:
June 01, 2025

Connect with a study center

  • COSDERMA

    Bordeaux, Gironde 33000
    France

    Active - Recruiting

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