跳至主要内容
临床试验/jRCT2080221906
jRCT2080221906未知3 期

A Phase 3, Multicenter, Randomized, Double-Blind,Placebo-Controlled Study to Evaluate the Efficacy and Safety of Subcutaneous LY2127399 in Patients with Systemic Lupus Erythematosus (SLE)

Parexel International0 个研究点开始时间: 待定

试验速览

阶段
3 期

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18age old over 至 No limit(—)
性别
All

入选标准

  • antinuclear antibodies (ANA) positive patients age 18 or older with active SLE without active lupus nephritis or active central nervous system (CNS) involvement

排除标准

  • 未提供

研究者

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