Status:
COMPLETED
A Clinical Study to Evaluate the Tolerability of a Topical Antibiotic and Retinoid Used in a Combined Regimen With a BPO Wash
Lead Sponsor:
Stiefel, a GSK Company
Collaborating Sponsors:
GlaxoSmithKline
Conditions:
Acne Vulgaris
Eligibility:
All Genders
12-45 years
Phase:
PHASE3
Brief 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
- 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
- Use of topical antibiotics on the face within the past 2 weeks or use of systemic antibiotics within the past 4 weeks.
Key Trial Info
Start Date :
April 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 5 2009
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT00891982
Start Date
April 1 2009
End Date
June 5 2009
Last Update
May 24 2017
Active Locations (5)
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1
Dermatology Associates Research
Coral Gables, Florida, United States, 33134
2
Grekin Skin Institute
Warren, Michigan, United States, 48088
3
Dermatology Consulting Services
High Point, North Carolina, United States, 27262
4
The Skin Wellness Center, PC
Knoxville, Tennessee, United States, 37922