Actively Recruiting

Phase 2
Age: 18Years +
All Genders
Healthy Volunteers
NCT06952517

Efficacy and Safety of Topical Clascoterone (WINLEVI) Cream 1% in Patients With Facial Acneiform Rosacea

Led by Narrows Institute for Biomedical Research · Updated on 2025-05-06

20

Participants Needed

1

Research Sites

28 weeks

Total Duration

On this page

Sponsors

N

Narrows Institute for Biomedical Research

Lead Sponsor

S

Sun Pharmaceutical Industries Limited

Collaborating Sponsor

AI-Summary

What this Trial Is About

To demonstrate the efficacy of Clascoterone cream 1% in reducing the size of sebaceous glands in study participants with acneiform rosacea.

CONDITIONS

Official Title

Efficacy and Safety of Topical Clascoterone (WINLEVI) Cream 1% in Patients With Facial Acneiform Rosacea

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women ages 18 and older
  • Diagnosed with rosacea type 2 (papulopustular)
  • Willing and able to follow study instructions and attend all visits
  • Able and willing to provide written and verbal informed consent
  • Used the same type and brand of makeup and facial and hair products for at least one month before baseline and agree to continue their use during the study
Not Eligible

You will not qualify if you...

  • Any skin condition that could affect evaluation or requires interfering topical or systemic therapy
  • Any condition that makes participation unsafe as judged by the investigator
  • Pregnant, lactating, or planning pregnancy during the study
  • Currently enrolled in another investigational drug or device study
  • Received investigational drug or device treatment within 30 days before starting
  • Facial hair that could interfere with study assessments as judged by the investigator
  • Unable to communicate or cooperate due to language, mental development, or brain function issues
  • Known allergy or hypersensitivity to any component of the study products
  • Plans or need to use artificial tanning or have excessive sun exposure during the trial

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

New York Harbor VA Brooklyn Campus

Brooklyn, New York, United States, 11209

Actively Recruiting

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Research Team

K

Kayla N Zafar, BA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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