Clinical trial Recruiting at 1 site Interventional Ages 12 to 55

Topical clascoterone vs. adapalene for mild-to-moderate acne in teens and young adults

Official title: Comparison of Topical Clascoterone 1% Cream Versus Adapalene 0.1% Cream in the Treatment of Mild-to-Moderate Acne Vulgaris

Run by Pak Emirates Military Hospital · NCT07883538 · Data updated 2026-11-12

This trial tests whether clascoterone 1% cream works as well as adapalene 0.1% cream for treating mild-to-moderate acne in people aged 12–55.

More Acne Vulgaris trials

Quick facts

Study typeInterventional
Ages12 Years to 55 Years
SexAll
Enrollment130 (estimated)
SponsorPak Emirates Military Hospital
Academic / other
Locations1 site (Rawalpindi, Punjab Province)
StatusRecruiting
StartedOctober 8, 2026
Main results expectedApril 30, 2027
Study endsApril 30, 2027
Registry record updatedOctober 22, 2026
Trial IDNCT07883538 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are males and females aged 12–55 with clinically diagnosed mild-to-moderate acne who agree to follow the treatment and follow-up visits.

Probably not a fit

Some participants may not experience clear or almost clear skin despite treatment, or may have adverse effects that limit benefit.

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

What this trial studies

This randomized controlled trial compares two topical acne treatments, clascoterone 1% cream applied twice daily and adapalene 0.1% cream applied once daily at night, over 12 weeks in patients with mild-to-moderate acne vulgaris. Participants will be evaluated at baseline, 4, 8, and 12 weeks using the Investigator's Global Assessment and lesion counts to determine treatment success (IGA 0 or 1). The study aims to determine which cream provides better skin clearance and safety in a dermatology outpatient setting in Rawalpindi, Pakistan. Both groups receive standard skincare advice, including gentle cleansing, moisturizers, sun protection, and avoidance of lesion picking. The trial will enroll 130 participants aged 12–55 years who meet the eligibility criteria.

Why it matters

Potential benefit: If clascoterone proves as effective or better than adapalene, patients may have an alternative topical option with a similar safety profile.

How similar studies have gone: Previous studies with clascoterone and with adapalene individually show activity in acne; direct head-to-head data are limited, making this comparative trial informative.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patients with clinically diagnosed mild-to-moderate acne vulgaris.
2. Patients willing to use the assigned treatment and attend scheduled follow-up visits.
3. Any gender between the ages of 12 and 55.

Exclusion Criteria:

1. Acne-like eruptions caused by drugs or another identifiable condition.
2. Recent topical or systemic anti-acne treatment that may affect assessment of the study treatment.
3. Pregnancy or breastfeeding as both these treatments are contraindicated.
4. Known allergy or hypersensitivity to clascoterone, adapalene or their formulation components.

Where it's running

  • Pak Emirates Military Hospital
    Rawalpindi, Punjab Province, Pakistan
    Recruiting

Study contacts

  • Principal investigator: dr Zeshan akhtar, MBBS — Pak Emiratres MIlitary Hospital Rawalpindi Pakistan
  • Study coordinator: Dr Zeshan Akhtar, MBBS
  • Email: zeshanakhtar367@gmail.com
  • Phone: +923215767900

Similar studies

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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.