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银屑病患者中,每周两次25毫克依那西普与每周一次50毫克依那西普的临床和药代动力学特征比较。

Comparison of clinical and pharmacokinetic profiles of etanercept 25 mg twice weekly and 50 mg once weekly in patients with psoriasis.

作者信息

Elewski B, Leonardi C, Gottlieb A B, Strober B E, Simiens M A, Dunn M, Jahreis A

机构信息

Uniuversity of Alabama at Birmingham, 700 18th Street S., Birmingham, AL 35233, USA.

出版信息

Br J Dermatol. 2007 Jan;156(1):138-42. doi: 10.1111/j.1365-2133.2006.07585.x.

Abstract

BACKGROUND

Etanercept is a tumour necrosis factor antagonist that is approved in the U.S.A., Canada and Europe for treating adult patients with chronic moderate to severe plaque psoriasis.

OBJECTIVES

To assess whether clinical efficacy, safety and pharmacokinetic (PK) profiles of etanercept 50 mg once weekly are comparable to etanercept 25 mg twice weekly.

METHODS

Patients from a U.S. phase 3 study and a global phase 3 study were subsequently enrolled in an open-label extension study (extension study) where they all received etanercept at a dose of 50 mg once weekly for an initial 12 weeks. Patients who had received at least 24 weeks of etanercept 25 mg twice weekly in the global phase 3 study and were enrolled in the extension study (n = 265) were assessed for efficacy and safety at extension study baseline and after 12 weeks of etanercept 50 mg once weekly. Efficacy endpoints included the Psoriasis Area and Severity Index (PASI), the Dermatology Life Quality Index and the Physician's Global Assessment of psoriasis. In addition, PK profiles from patients in the U.S. phase 3 study were compared with PK profiles from another set of patients in the extension study. Comparison was made between a subset of patients receiving etanercept 25 mg twice weekly dosing in the U.S. phase 3 study (n = 13) and those receiving etanercept 50 mg once weekly in the extension study (n = 84).

RESULTS

The mean PASI score was 5.77 at extension study baseline after treatment with etanercept 25 mg twice weekly, which was sustained at 5.82 after 12 weeks of etanercept 50 mg once weekly. Similar results were observed in other efficacy endpoints. Etanercept 50 mg once weekly was generally well tolerated. No new safety findings were reported. PK profiles overlapped extensively between the two dosing regimens.

CONCLUSIONS

In this report, we demonstrate that efficacy, safety and PK profiles were comparable between etanercept 25 mg twice weekly and 50 mg once weekly in patients who had received at least 24 weeks of etanercept 25 mg twice weekly prior to receiving etanercept 50 mg once weekly in the extension study.

摘要

背景

依那西普是一种肿瘤坏死因子拮抗剂,在美国、加拿大和欧洲被批准用于治疗患有慢性中度至重度斑块状银屑病的成年患者。

目的

评估每周一次50毫克依那西普的临床疗效、安全性和药代动力学(PK)特征是否与每周两次25毫克依那西普相当。

方法

来自一项美国3期研究和一项全球3期研究的患者随后被纳入一项开放标签扩展研究(扩展研究),在该研究中,他们均接受初始12周每周一次50毫克剂量的依那西普治疗。在全球3期研究中接受至少24周每周两次25毫克依那西普治疗并被纳入扩展研究的患者(n = 265),在扩展研究基线以及接受每周一次50毫克依那西普治疗12周后进行疗效和安全性评估。疗效终点包括银屑病面积和严重程度指数(PASI)、皮肤病生活质量指数以及医生对银屑病的整体评估。此外,将美国3期研究患者的PK特征与扩展研究中另一组患者的PK特征进行比较。比较了美国3期研究中接受每周两次25毫克依那西普给药的一部分患者(n = 13)与扩展研究中接受每周一次50毫克依那西普的患者(n = 84)。

结果

在每周两次25毫克依那西普治疗后,扩展研究基线时的平均PASI评分为5.77,在每周一次50毫克依那西普治疗12周后维持在5.82。在其他疗效终点观察到类似结果。每周一次50毫克依那西普总体耐受性良好。未报告新的安全性发现。两种给药方案的PK特征广泛重叠。

结论

在本报告中,我们证明,对于在扩展研究中接受每周一次50毫克依那西普治疗之前已接受至少24周每周两次25毫克依那西普治疗的患者,每周两次25毫克依那西普与每周一次50毫克依那西普在疗效、安全性和PK特征方面相当。

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