跳至主要内容
临床试验/NCT00143806
NCT00143806已完成2 期

Investigator-Initiated, Use Study of Alefacept (Amevive) in Combination With Tapering Doses of Cyclosporine in Patients With Moderate to Severe Psoriasis

University of Medicine and Dentistry of New Jersey2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2003年10月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
13
试验地点
2
主要终点
Static physicians global assessment (PGA) and quality of life as measured by DLQI

研究概览

简要总结

The purpose of this study is to devise a safe and effective method for transitioning patients from cyclosporine to alefacept.

详细描述

The purpose of this study is to devise a safe and effective method for transitioning patients from cyclosporine to alefacept. Patients in the study are well controlled on cyclosporine and desire to switch to alefacept. The study is done in three phases. In Phase 1 (12 week duration) the two drugs will be overlapped, with cyclosporine slowly tapering. Both drugs will be discontinued after 12 weeks. In Phase 2 (12 weeks duration), patients are off both drugs. In Phase 3 (24 weeks long), patients are on a second course of alefacept alone for 12 weeks and then off for 12 weeks. Topical and UV light treatments are allowed throughout the study. Total length of study is one year.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Static physicians global assessment (PGA) and quality of life as measured by DLQI

次要结局

未报告次要终点

研究者

研究点 (2)

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