Calcipotriene Plus Betamethasone Dipropionate Topical Suspension for the Treatment of Mild to Moderate Psoriasis Vulgaris on the Body: A Randomized, Double-Blind, Vehicle-Controlled Trial

被引:0
|
作者
Menter, Alan [1 ]
Gold, Linda Stein [2 ]
Bulchalo, Michael [3 ]
Grekin, Steven [4 ]
Kempers, Steven [5 ]
Boyce, Brent M. [6 ]
Ganslandt, Cecilia [7 ]
Villumsen, John [8 ]
Lebwohl, Mark [9 ]
机构
[1] Baylor Univ, Med Ctr, Dept Dermatol, Dallas, TX USA
[2] Henry Ford Hlth Syst, Dept Dermatol, Detroit, MI USA
[3] Altman Dermatol Associates, Arlington Hts, IL USA
[4] Grekin Skin Inst, Warren, MI USA
[5] Minnesota Clin Study Ctr, Fridley, MN USA
[6] Great Lakes Res Grp Inc, Bay City, MI USA
[7] LEO Pharma AS, Dept Med, Ballerup, Denmark
[8] LEO Pharma AS, Dept Biostat, Ballerup, Denmark
[9] Mt Sinai Sch Med, Dept Dermatol, New York, NY USA
关键词
QUALITY-OF-LIFE; SCALP FORMULATION; ACTIVE INGREDIENTS; ADHERENCE; MANAGEMENT; EFFICACY; SAFETY;
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background/Objectives: A combination topical suspension/gel containing calcipotriene plus betamethasone dipropionate has been developed as a safe and effective treatment for patients with psoriasis vulgaris of the scalp. This same preparation has the potential to be a convenient, effective, and cosmetically appealing formulation for psoriasis on the body. This trial evaluated the efficacy and safety of a topical suspension containing calcipotriene plus betamethasone dipropionate compared with its constituent components and topical suspension vehicle in the treatment of mild to moderate psoriasis on the trunk and limbs. Methods: This was a randomized, double-blind, vehicle-controlled, 4-arm trial in 1,152 subjects. The co-primary efficacy end points were the proportion of subjects achieving controlled disease based on the Investigators' Global Assessment of disease severity at weeks 4 and 8. Adverse events, vital signs, and clinical laboratory measurements were also assessed. Results: At week 4, a greater proportion of subjects in the calcipotriene plus betamethasone group achieved controlled disease compared with subjects in the calcipotriene-only and vehicle-only treatment groups. At week 8, a statistically significantly (P<.01) greater proportion of subjects in the calcipotriene plus betamethasone group achieved controlled disease compared with subjects in the 3 other treatment groups. Adverse events and other safety assessments were similar between the groups. Conclusion: The topical suspension containing calcipotriene plus betamethasone dipropionate traditionally used for scalp psoriasis is also a safe and effective once-daily treatment for psoriasis vulgaris on the body. J Drugs Dermatol. 2013;12(1):92-98.
引用
收藏
页码:92 / 98
页数:7
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