Abstract | BACKGROUND: OBJECTIVES: To compare the efficacy and tolerability in combination of CDP/BPO in comparison with ADA in Asian patients with mild to moderate acne vulgaris. METHODS: Total of 69 patients, including 31 patients for CDP/BPO group and 38 for ADA group, with mild to moderate acne vulgaris were enrolled for a 12-week prospective, randomized, open-label comparative study of topical agents. Efficacy was assessed by lesion counts, acne grading system, and global improvement. Adverse events were also evaluated in scale of 0 (none) to 3 (severe). RESULTS: Both CDP/BPO and ADA were effective in reducing lesion counts and acne severity scale and showed significant global improvement. However, CDP/BPO offered greater efficacy against inflammatory lesions than ADA. Both drugs were well tolerated with minimal adverse drug reactions. CONCLUSION: Combination formulation of CDP/BPO and ADA were shown to be both effective in decreasing total, inflammatory, and non-inflammatory lesion counts along with well tolerability in Asian patients with mild to moderate acne vulgaris.
|
Authors | H-C Ko, M Song, S-H Seo, C-K Oh, K-S Kwon, M-B Kim |
Journal | Journal of the European Academy of Dermatology and Venereology : JEADV
(J Eur Acad Dermatol Venereol)
Vol. 23
Issue 3
Pg. 245-50
(Mar 2009)
ISSN: 1468-3083 [Electronic] England |
PMID | 19438817
(Publication Type: Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Drug Combinations
- Gels
- Naphthalenes
- Adapalene
- Clindamycin
- Benzoyl Peroxide
|
Topics |
- Acne Vulgaris
(drug therapy)
- Adapalene
- Adult
- Benzoyl Peroxide
(administration & dosage, therapeutic use)
- Clindamycin
(administration & dosage, therapeutic use)
- Drug Combinations
- Female
- Gels
- Humans
- Male
- Naphthalenes
(administration & dosage, therapeutic use)
- Prospective Studies
|