Safety and efficacy of pimecrolimus (ASM 981) cream 1% in the treatment of mild and moderate atopic dermatitis in children and adolescents

被引:263
作者
Eichenfield, LF
Lucky, AW
Boguniewicz, M
机构
[1] Childrens Hosp, San Diego, CA 92123 USA
[2] Univ Calif San Diego, Sch Med, San Diego, CA 92103 USA
[3] Dermatol Res Associates, Cincinnati, OH USA
[4] Natl Jewish Med & Res Ctr, Denver, CO USA
[5] QE2 Hlth Sci Ctr, Halifax, NS, Canada
[6] Novartis Pharmaceut, E Hanover, NJ USA
[7] Novartis Pharma AG, Basel, Switzerland
关键词
D O I
10.1067/mjd.2002.122187
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background. The ascomycin derivative pimecrolimus (ASM 981) is a cell-selective cytokine inhibitor, specifically developed for the treatment of inflammatory skin diseases. Objective: When applied topically, pimecrolimus cream 1% has shown promise as a treatment for inflammatory skin conditions, including atopic dermatitis (AD) in children and adults, allergic contact dermatitis, and chronic contact irritant hand dermatitis in adults. Methods: In two independent 6-week, randomized, multicenter studies of identical design, the efficacy and safety of pimecrolimus cream 1% in children with predominantly moderate AD were compared with vehicle. Pooled data from a total of 403 patients were used in the analysis. The primary efficacy parameter was the Investigator's Global Assessment (IGA) score. Secondary parameters included Eczema Area and Severity Index (EASI) and severity of pruritus scores. Subjects were also asked to assess their disease control as uncontrolled, limited, good, or complete. Results: Significant therapeutic benefits relative to vehicle were observed in the pimecrolimus-treated group at the first efficacy assessment, 8 days after initial application of the study medication (eg, relief of pruritus). At each subsequent postbaseline visit, pimecrolimus-treated patients showed significant improvement relative to controls in all efficacy measures. The medication was well tolerated. Conclusion: Pimecrolimus cream 1% appears to be a safe and effective alternative to currently used therapies for AD.
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页码:495 / 504
页数:10
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