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临床试验/JPRN-jRCT2080221610
JPRN-jRCT2080221610未知1 期

A Phase 1/2, Single-arm, Open-label Study of SGN-35 in Japanese Patients with relapsed/refractory CD30-positive Hodgkin Lymphoma or Systemic Anaplastic Large Cell Lymphoma

Takeda Pharmaceutical Company Limited0 个研究点目标入组 17 人开始时间: 2011年10月7日最近更新:
适应症

试验速览

阶段
1 期
入组人数
17

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Major inclusion criteria include the following:
  • 1) CD30-positive HL or sALCL
  • 2) Patients who had PD during the standard chemo therapy OR who did not have CR/PR OR who had a recurrence or reprogression after the standard chemo therapy
  • 3) Patients with HL must have been ineligible for, refused treatment by or previously received ASCT
  • 4) Eastern Cooperative Oncology Group (ECOG) Performance Status: 0 or 1
  • 5) Adequate hematologic, renal and liver function

排除标准

  • Major exclusion criteria include the following:
  • 1) Primary cutaneous ALCL
  • 2) Uncontrolled diabetes
  • 3) Patients with known cerebral/meningeal disease
  • 4) Patients with history of allogeneic stem cell transplant
  • 5) Patients with a history of another malignancy

研究者

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