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子囊霉素大环内酯类药物SDZ ASM 981用于特应性皮炎局部治疗的有效性。

Effectiveness of the ascomycin macrolactam SDZ ASM 981 in the topical treatment of atopic dermatitis.

作者信息

Van Leent E J, Gräber M, Thurston M, Wagenaar A, Spuls P I, Bos J D

机构信息

Department of Dermatology, Academic Medical Center, University of Amsterdam, The Netherlands.

出版信息

Arch Dermatol. 1998 Jul;134(7):805-9. doi: 10.1001/archderm.134.7.805.

Abstract

OBJECTIVE

To compare the safety and efficacy of 1% SDZ ASM 981 cream and a matching placebo cream in the treatment of patients with moderate atopic dermatitis.

DESIGN

A randomized, double-blind, placebo-controlled, right-and-left comparison study.

SETTING

Academic referral center.

PATIENTS

Thirty-four adult patients with moderate atopic dermatitis.

INTERVENTION

Topical 1% SDZ ASM 981 cream was applied twice daily (n=16) or once daily (n=18) and compared with a corresponding placebo cream base.

MAIN OUTCOME MEASURES

Efficacy was measured using a 4-point (0-3) scale for erythema, pruritus, exudation, excoriation, and lichenification (Atopic Dermatitis Severity Index [ADSI]). The ADSI score was defined as the sum of these 5 ratings (range, 0-15) and was determined on the pretreatment day (1 to 14 days before day 0) and on days 0, 2, 4, 7, 9, 11, 14, 16, 18, and 21. The percentage change from baseline (day 0) in the ADSI score was calculated on each of these days. Safety was evaluated by monitoring of adverse events, physical examination, hematologic examination, clinical chemistry studies, urinalysis, and measurement of blood levels of SDZ ASM 981.

RESULTS

Of the 38 patients recruited, 34 started and 28 completed treatment according to the protocol. Sixteen patients used the cream twice daily, with significant improvement after 2 days of treatment. Within 3 weeks of topical therapy with 1% SDZ ASM 981 cream twice daily, a mean reduction of 71.9% in the ADSI score was observed at the actively treated test sites compared with a mean reduction of 10.3% at the placebo-treated test sites (P<.001). Efficacy was significantly less in the group treated once daily (n=18), with mean reductions of 37.7% and 6.2%, respectively. The efficacy was especially apparent for pruritus and excoriation. There were no clinically relevant drug-related adverse effects.

CONCLUSIONS

Treatment with 1% SDZ ASM 981 cream was well tolerated. Twice-daily application of 1% SDZ ASM 981 cream was significantly more effective than use of the corresponding placebo and more effective than once-daily treatment. The new macrolactam ascomycin derivative SDZ ASM 981 is a promising agent for the treatment of patients with atopic dermatitis. More elaborate phase 2 and 3 trials are under way to fully investigate the potential of this medication.

摘要

目的

比较1% SDZ ASM 981乳膏与匹配的安慰剂乳膏治疗中度特应性皮炎患者的安全性和疗效。

设计

一项随机、双盲、安慰剂对照、左右比较研究。

地点

学术转诊中心。

患者

34例中度特应性皮炎成年患者。

干预

外用1% SDZ ASM 981乳膏,每日两次(n = 16)或每日一次(n = 18),并与相应的安慰剂乳膏基质进行比较。

主要观察指标

使用4分制(0 - 3)量表评估红斑、瘙痒、渗出、抓痕和苔藓化情况(特应性皮炎严重程度指数[ADSI])。ADSI评分定义为这5项评分之和(范围0 - 15),在治疗前一天(第0天前1至14天)以及第0、2、4、7、9、11、14、16、18和21天进行测定。计算这些天中ADSI评分相对于基线(第0天)的变化百分比。通过监测不良事件、体格检查、血液学检查、临床化学研究、尿液分析以及测定SDZ ASM 981的血药浓度来评估安全性。

结果

招募的38例患者中,34例开始治疗,28例按方案完成治疗。16例患者每日使用乳膏两次,治疗2天后有显著改善。在每日两次外用1% SDZ ASM 981乳膏的3周内,与安慰剂治疗的试验部位相比,积极治疗的试验部位ADSI评分平均降低71.9%,而安慰剂治疗部位平均降低10.3%(P <.001)。每日一次治疗组(n = 18)的疗效明显较差,平均降低率分别为37.7%和6.2%。瘙痒和抓痕方面的疗效尤为明显。未出现临床相关的药物相关不良反应。

结论

1% SDZ ASM 981乳膏治疗耐受性良好。每日两次外用1% SDZ ASM 981乳膏比使用相应安慰剂显著更有效,且比每日一次治疗更有效。新型大环内酯类子囊霉素衍生物SDZ ASM 981是治疗特应性皮炎患者的一种有前景的药物。正在进行更详细精心的2期和3期试验以全面研究该药物的潜力。

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