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

NCT00891982

CompletedPhase 3

Sponsor: Stiefel, a GSK Company

Conditions: Acne Vulgaris

Interventions: CTGel/ BPO Wash, Soap Free Cleanser and CTGel

Countries: United States

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 overview

Sex: ALL

Age: 12 Years to 45 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* 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.

Exclusion Criteria:

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

Locations (5)

Coral Gables, Florida, United States
Warren, Michigan, United States
High Point, North Carolina, United States
Knoxville, Tennessee, United States
Spokane, Washington, United States