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临床试验/EUCTR2012-001610-42-PT
EUCTR2012-001610-42-PT进行中(未招募)不适用

A Randomized, Double-masked, Placebo-controlled Study of the Safety and Efficacy of Gevokizumab in the Treatment of Active Non-infectious Intermediate, Posterior, or Pan- Uveitis

XOMA (US) LLC0 个研究点目标入组 300 人开始时间: 2012年9月24日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
XOMA (US) LLC
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Diagnosis of non-infectious intermediate, posterior, or pan-uveitis in at least one eye fulfilling the International Study Group Classification Criteria ([SUN] criteria) of intermediate, posterior, or pan- uveitis confirmed by documented medical history
  • - Active uveitic disease, defined by the presence of = 2+ vitreous haze score in at least one eye
  • - Best Corrected Visual Acuity of 10 to 75 letters in the study eye
  • - Patients with a stable background treatment of oral corticosteroids, selected immunosuppressive therapy, or combination of both.
  • - Male or female, age =18 (or legal age of majority in the country) at selection
  • - For subjects with reproductive potential, a willingness to use highly effective contraceptive measures.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 270
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 30

排除标准

  • - Infectious uveitis and masquerade syndromes
  • - Isolated anterior uveitis
  • - Best corrected visual acuity < 35 letters in the non-study eye or monocular vision
  • - Presence of severe cataract or severe posterior capsular opacification.
  • - Contraindication to mydriatics or presence of posterior synechiae.
  • - Active TB disease.
  • - History of severe allergic or anaphylactic reactions to monoclonal antibodies
  • - History of malignancy within 5 years prior to Selection.
  • - Infectious disease.
  • - Known immunodeficiency.
  • - Pregnancy, breastfeeding or possibility to become pregnant during the study

研究者

发起方
XOMA (US) LLC

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