Clinical trial Recruiting at 1 site Interventional Ages 14 to 24

Comparing a cosmetic product for treating facial acne in young adults

Official title: A Randomized Investigator-blinded Comparative Study to Assess the Efficacy of the Cosmetic Care Product RV4133C - Formula JT2559 in Subjects With Facial Acne, During a 3-month-associated-treatment Phase Followed by a 3-month-maintenance Phase

Run by Pierre Fabre Dermo Cosmetique · NCT06716398 · Data updated 2026-11-12

This study tests whether a new cosmetic product can help teenagers and young adults with acne when used alongside their regular acne treatment.

More Acne trials

Quick facts

Study typeInterventional
Ages14 Years to 24 Years
SexAll
Enrollment60 (estimated)
SponsorPierre Fabre Dermo Cosmetique
Industry-sponsored
Locations1 site (São Paulo)
StatusRecruiting
StartedJuly 3, 2024
Main results expectedJuly 30, 2025
Study endsJuly 30, 2025
Registry record updatedDecember 4, 2024
Trial IDNCT06716398 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are males and females aged 14 to 24 with mild to moderate facial acne.

Probably not a fit

Patients with severe forms of acne or other facial skin diseases may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of a cosmetic product as complementary care alongside a prescribed topical medical treatment for facial acne in teenagers and young adults. Participants will undergo a 3-month associated treatment phase followed by a 3-month maintenance phase, during which the cosmetic product will be compared to a light moisturizing cream. The study aims to assess both the global benefits and the tolerance of the tested product in conjunction with the medical treatment.

Why it matters

Potential benefit: If successful, this study could provide an effective cosmetic solution to enhance acne treatment outcomes for young patients.

How similar studies have gone: Other studies have shown promising results with similar approaches in improving acne treatment outcomes.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Male or Female aged between 14 and 24 years (included)
* Subject with facial acne with score index severity IGA = 2 or 3, assessed on a scale ranged from 0 to 4.
* Subject for whom a prescription of 12 weeks of a reference topical medical treatment is required from the day of the inclusion visit, for mild to moderate face acne

Exclusion Criteria:

Criteria related to the disease:

* Facial skin disease other than acne, skin abnormalities, or dermatological condition on the face liable to interfere with the study assessments
* Acne conglobata, Acne fulminans, nodulocystic acne or acneiform eruptions, according to investigator's assessment
* Other type of pigmentation disorder than acne-related PIH liable to interfere with the study assessments according to the investigator

Criteria related to treatments and/or products:

\- Topical or oral 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 or cutaneous tolerance of the investigational products

Where it's running

  • Unifesp
    São Paulo, Brazil
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.