跳至主要内容
临床试验/CTRI/2016/01/006493
CTRI/2016/01/006493进行中(未招募)3 期

A Phase 3, Randomised, Parallel-Group, Active-Controlled, Double Blind Study to Compare Efficacy and Safety between CT P10 and Rituxan in Patients with Low Tumour Burden Follicular Lymphoma - CT-P10 3.4

CELLTRION Inc0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
CELLTRION Inc

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

入选标准

  • Key brief inclusion criteria:
  • Confirmed diagnosis of low tumour burden, CD20+ follicular lymphoma grade 1 to 3a according to the World Health Organization 2008 classification
  • Ann Arbor Stage II, III or IV

排除标准

  • Key brief exclusion criteria:
  • Has received rituximab
  • Allergies or hypersensitivity to murine, chimeric, human or humanised proteins
  • Previous treatment for NHL
  • Any malignancy, patient has known central nervous system involvement or any evidence of spinal cord compression by lymphoma
  • Current or recent treatment with any other investigational medicinal product or device
  • pregnant or lactating

研究者

发起方
CELLTRION Inc

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