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A Comparative Study of the Tolerability of Two Combination Therapies for the Treatment of Acne
A Comparative Study of the Tolerability of Two Combination Therapies for the Treatment of Acne
CompletedPhase 4
Sponsor: Stiefel, a GSK Company
Conditions: Acne Vulgaris
Interventions: BENZOYL PEROXIDE/ CLINDAMYCIN, BENZOYL PEROXIDE/ ADAPALENE
Countries: Argentina
The purpose of this study is to compare the tolerability of topical combination therapies in the treatment of facial acne.
Eligibility overview
Sex: ALL
Age: 21 Years to —
Healthy volunteers: No
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * Male or female subjects at least 21 years of age, in good general health with documented diagnosis of acne vulgaris. * Female subjects of childbearing potential must have a negative pregnancy test. Sexually active women of childbearing potential participating in the study must use a medically acceptable form of contraception Abstinence is considered an acceptable method of contraception. * Inflammatory (papules and pustules) and non-inflammatory (open and closed comedones) facial lesions. * The ability and willingness to follow all study procedures, attend all scheduled visits, and successfully complete the study * Capable of understanding and willing to provide signed and dated written voluntary informed consent (and any local or national authorization requirements) before any protocol specific procedures are performed Exclusion Criteria: * Female subjects who are pregnant, trying to become pregnant or breastfeeding. * Subjects who have any clinically relevant finding at their baseline physical other than acne vulgaris. * History or presence of regional enteritis or inflammatory bowel disease (eg, ulcerative colitis, pseudomembranous colitis, chronic diarrhea, or a history of antibiotic-associated colitis) or similar symptoms. * Use of topical antibiotics or anti-acne medications on the face and systemic antibiotics within the past 2 and 4 weeks, respectively. * Use of topical corticosteroids on the face or systemic corticosteroids within the past 4 weeks. Use of inhaled, intra-articular or intra-lesional (other than for facial acne lesions) steroids is acceptable. * Use of systemic retinoids within the past 6 months. * Facial procedures performed by an esthetician, beautician, physician, nurse, or other practitioner, within the past 4 weeks or during the conduct of the study. * Known hypersensitivity or previous allergic reaction to any of the active components, lincomycin, adapalene, clindamycin, benzoyl peroxide or excipients of the study product.
Locations (4)
- Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
- Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
- Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
- Ciudad de Buenos Aires, Buenos Aires, Argentina