跳至主要内容
临床试验/CTRI/2009/091/000566
CTRI/2009/091/000566已完成2 期

Phase II Safety and Efficacy Study of the Monoclonal Antibody CT-011 in Patients with Diffuse Large B-Cell Lymphoma following Autologous Stem Cell Transplantation

CureTech Ltd0 个研究点目标入组 68 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
CureTech Ltd
入组人数
68

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

  • 1.Patient's age is 18 years or older, both genders.
  • 2.Confirmed Diffuse Large B-cell Lymphoma, transformed follicular lymphoma, diffuse mixed cell lymphoma or primary mediastinal large cell lymphoma with B-cell lineage.
  • 3.The lymphoma is chemosensitive.
  • 4.The lymphoma did not progress since pre-transplant chemotherapy.
  • 5.ECOG performance status 0-1.

排除标准

  • 1.Serious other illness.
  • 2.Active autoimmune disease.
  • 3.Type 1 diabetes.
  • 4.Known immune deficiency.
  • 5.Clinical evidence of primary or secondary brain or spinal cord involvement by lymphoma.
  • 6.Active bacterial, fungal, or viral infection.
  • 7.Positive HIV, Hepatitis B surface antigen plus viremia, or Hepatitis C antibody plus viremia.
  • 8.Pregnant or nursing (positive pregnancy test).
  • 9.Other concurrent clinical study or investigational therapy.

研究者

发起方
CureTech Ltd

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