A Clinical Study to Evaluate the Tolerability of a Topical Antibiotic and Retinoid Used in a Combined Regimen With a BPO Wash

Last updated: May 19, 2017
Sponsor: Stiefel, a GSK Company
Overall Status: Completed

Phase

3

Condition

Rash

Acne

Scalp Disorders

Treatment

N/A

Clinical Study ID

NCT00891982
114679
  • Ages 12-45
  • All Genders

Study Summary

The purpose of this study is to evaluate the tolerability of a combined regimen of a topical antibiotic and retinoid and a benzoyl peroxide wash.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Subjects with mild to moderate facial acne vulgaris, with no history of known orsuspected hypersensitivity or previous allergic reaction to any of the ingredients ofthe study products (eg, topical antibiotics, retinoids or benzoyl peroxide), capableof understanding and willing to provide signed and dated written voluntary informedconsent and able to complete the study and to comply with study instructions.

  • Female subjects of childbearing potential must have a negative urine pregnancy testresult at baseline and practice a reliable method of contraception throughout thestudy.

Exclusion

Exclusion Criteria:

  • Use of topical antibiotics on the face within the past 2 weeks or use of systemicantibiotics within the past 4 weeks.

Study Design

Total Participants: 60
Study Start date:
April 01, 2009
Estimated Completion Date:
June 05, 2009

Connect with a study center

  • Dermatology Associates Research

    Coral Gables, Florida 33134
    United States

    Site Not Available

  • Grekin Skin Institute

    Warren, Michigan 48088
    United States

    Site Not Available

  • Dermatology Consulting Services

    High Point, North Carolina 27262
    United States

    Site Not Available

  • The Skin Wellness Center, PC

    Knoxville, Tennessee 37922
    United States

    Site Not Available

  • Premier Clinical Research

    Spokane, Washington 99204
    United States

    Site Not Available

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