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临床试验/JPRN-jRCT2080222013
JPRN-jRCT2080222013未知3 期

Randomized, phase III, comparative study of every-3-weeks dosing, weekly dosing of ABI-007, and weekly dosing of the conventional paclitaxel for patients with unresectable/recurrent gastric cancer refractory to prior chemotherapy containing fluoropyrimidines.

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 730 人开始时间: 2013年1月28日最近更新:

试验速览

阶段
3 期
入组人数
730

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

  • Signed, written informed consent.
  • - Histologically or cytologically confirmed gastric adenocarcinoma.
  • - Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2.

排除标准

  • - Past history of severe drug hypersensitivity
  • - Patient has pre-existing peripheral neuropathy of Grade 2, 3, or 4 (per CTCAE).
  • - Principal Investigators'(sub investigators') judgment on ineligibility

研究者

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