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临床试验/PER-015-03
PER-015-03已完成1 期

CLINICAL TRIAL II OF IROFULVEN EVERY TWO WEEKS IN PATIENTS WITH IRRESECABLE HEPATOCELLULAR CARCINOMA

MGI PHARMA, INC.,0 个研究点目标入组 0 人开始时间: 2003年3月11日最近更新:

试验速览

阶段
1 期
状态
已完成
发起方

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

  • - The patient must sign the written informed consent approved by the institutional committee for scientific review (IRB).
  • - The patient must have a histological or cytological diagnosis of hepatocellular carcinoma that has been considered unresectable.
  • - The patient should not have more than one previous therapeutic intervention for the treatment of hepatocellular carcinoma including surgical techniques, ablative,
  • chemo-embolization, and systemic chemotherapy.

排除标准

  • - Previous treatment with gene therapy.
  • - Women who are pregnant or breast-feeding.
  • - Patients with any concomitant systemic disorder (in the opinion of the researcher)
  • - Patients who have completed or who have been withdrawn from this study or any other study with irofulven.

研究者

发起方
MGI PHARMA, INC.,

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