跳至主要内容
临床试验/NCT00096603
NCT00096603已完成3 期

An Open Label, Multicenter Study to Evaluate the Safety of 1.0 mg/kg Subcutaneously Administered Efalizumab in Adults With Plaque Psoriasis Previously Enrolled in Study ACD2600g

Genentech, Inc.0 个研究点目标入组 450 人开始时间: 2002年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
450

研究概览

简要总结

This is an open label, multicenter study designed to evaluate the safety and tolerability of efalizumab administered subcutaneously at weekly doses of 1.0 mg/kg in subjects with plaque psoriasis who previously participated in Study ACD2600g.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Signed informed consent
  • •Previous participation in Study ACD2600g
  • •For women of childbearing potential, continued use of an acceptable method of contraception for the duration of the study

排除标准

  • •Any medical condition that, in the judgment of the investigator, would jeopardize the subject's safety following exposure to Efalizumab

研究组 & 干预措施

未命名试验

干预措施: Raptiva (efalizumab) (Drug)

研究者

申办方类型
Industry
责任方
Sponsor

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