Hydrocortisone butyrate 0.1% lotion in the treatment of atopic dermatitis in pediatric subjects

被引:0
作者
Matheson, Robert [2 ]
Kempers, Steven [3 ]
Breneman, Debra [4 ]
Draelos, Zoe
Johnson, Candice E. [5 ]
Loss, Robert [6 ]
Hogan, Daniel J. [7 ]
Schoenfeld, Robert [8 ]
Checketts, Scott [9 ]
Kircik, Leon [10 ]
Fivenson, David [11 ]
Hebert, Adelaide A. [12 ]
Williams, Judith [13 ]
Hamlin, Regina [14 ]
Groisser, Daniel [15 ]
Piacquadio, Dan [1 ,16 ]
机构
[1] Therapeut Inc, San Diego, CA 92123 USA
[2] Oregon Med Res Ctr, Portland, OR USA
[3] Minnesota Clin Study Ctr, Fridley, MN USA
[4] Univ Cincinnati, Dept Dermatol, Cincinnati, OH USA
[5] Childrens Hosp, Denver, CO 80218 USA
[6] Dermatol Associates Rochester PC, Rochester, NY USA
[7] Louisiana State Univ, Hlth Sci Ctr, Shreveport, LA 71105 USA
[8] Wayne State Univ, Dept Dermatol, Detroit, MI USA
[9] Tanner Mem Clin, Layton, UT USA
[10] DermRes PLLC, Louisville, KY USA
[11] Dermatol PLLC, Ann Arbor, MI USA
[12] Univ Texas Houston, Hlth Sci Ctr, Houston, TX USA
[13] Childrens Hosp Kings Daughters, Norfolk, VA USA
[14] Associates Res Inc, Fresno, CA USA
[15] Dermal Grp PC, Verona, NJ USA
[16] Univ Calif San Diego, Div Dermatol, San Diego, CA 92103 USA
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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: Hydrocortisone butyrate (HCB) is currently marketed as a cream, ointment, and solution. A new lotion formulation of hydrocortisone butyrate 0.1% (Locoid (R) lotion) has been developed and evaluated. Objective: The objective of this study was to evaluate the efficacy and safety of HCB 0.1% lotion compared to the vehicle in subjects aged 3 months to less than 18 years with mild to moderate atopic dermatitis (AD). Methods: In this multicenter double-blind study, 284 subjects with mild to moderate AD were randomized 1: 1 to receive HCB 0.1% lotion or the vehicle for a duration of 4 weeks. "Treatment success" was defined as those subjects with a final Physician Global Assessment (PGA) score of 0 or 1 that had at least a 2-point reduction in the PGA score from baseline to day 29. Safety was assessed by monitoring adverse events. Results: Analyses of the final PGA score showed a significant treatment effect (P<.001) in favor of the HCB 0.1% lotion group. The safety profile of the HCB 0.1% lotion was also favorable. Limitations: The study did not assess the durability of the treatment effects (ie, safety and efficacy) after completion of the 4-week treatment period nor the potential need for longer term therapy given the chronic nature of AD. Conclusion: Results demonstrate the safety and efficacy of HCB 0.1% lotion in the treatment of mild to moderate AD in children 3 months to 18 years of age.
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页码:266 / 271
页数:6
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