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

Completed · Phase 3

Conditions studied: Acne Vulgaris

In brief

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.

Key facts

Study ID

NCT00891982

Run by

Stiefel, a GSK Company

People needed

60

Starts

2009-04-01

Expected to finish

2009-06-05

Last updated by the study team

2017-05-24

Who can join

Age: 12 and older, up to 45. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects with mild to moderate facial acne vulgaris, with no history of known or suspected hypersensitivity or previous allergic reaction to any of the ingredients of the study products (eg, topical antibiotics, retinoids or benzoyl peroxide), capable of understanding and willing to provide signed and dated written voluntary informed consent and able to complete the study and to comply with study instructions.
• Female subjects of childbearing potential must have a negative urine pregnancy test result at baseline and practice a reliable method of contraception throughout the study.

You may not qualify if…

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

Where it is running

• Dermatology Associates Research — Coral Gables, Florida, United States
• Grekin Skin Institute — Warren, Michigan, United States
• Dermatology Consulting Services — High Point, North Carolina, United States
• The Skin Wellness Center, PC — Knoxville, Tennessee, United States
• Premier Clinical Research — Spokane, Washington, United States

Full record on ClinicalTrials.gov

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