跳至主要内容
临床试验/EUCTR2016-003202-14-PT
EUCTR2016-003202-14-PT进行中(未招募)1 期

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study of the Bruton’s Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Combination with Rituximab versus Placebo in Combination with Rituximab in Treatment Naïve Subjects with Follicular Lymphoma - PERSPECTIVE

Pharmacyclics LLC0 个研究点目标入组 440 人开始时间: 2017年3月24日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
440

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

  • * Histologically confirmed diagnosis of follicular lymphoma CD20+ (Grade 1, 2 or 3a) Ann Arbor Stage II, III or IV disease.
  • * Measurable disease
  • * Subjects 70 years of age or older; OR subjects 60-69 years of age who have one or more comorbidities.
  • * Meets one or more Groupe d'Etude des Lymphomes Folliculaire (GELF) criteria.
  • * Adequate hematologic function within protocol-defined parameters.
  • * Adequate hepatic and renal function within protocol-defined parameters.
  • * ECOG performance status score of 0-2.
  • 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 240
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 200

排除标准

  • * Transformed lymphoma
  • * Prior treatment for follicular lymphoma
  • * Central nervous system lymphoma or leptomeningeal disease
  • * Currently active, clinically significant cardiovascular disease

研究者

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