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临床试验/PER-056-02
PER-056-02已完成未知

CLINICAL PHASE II STUDY OF IROFULVEN IN COMBINATION WITH IRINOTECAN IN PATIENTS WITH ADVANCED SOLID TUMORS GASTROINTESTINALES

MGI PHARMA, INC.,0 个研究点目标入组 0 人开始时间: 2002年8月23日最近更新:
适应症

试验速览

阶段
未知
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

  • Patients with advanced gastrointestinal solid tumors without standard chemotherapy treatment or progressed to standard chemotherapy.
  • Disease measurable / evaluable by the RECIST criteria.
  • Age 18 years.
  • ECOG Performance Status (PS): 0-1
  • Life expectancy> 3 months.

排除标准

  • Previous chemotherapy with topoisomerase I inhibitors
  • Previous intestinal obstruction / subostruction not completely resolved or chronic diarrhea, chronic enteropathy, extensive intestinal resection (> hemicolectomy).
  • Patients with radiant treatment in more than 35% of the bone marrow after admission to the study.
  • Presence of any serious concomitant systemic disorder incompatible with the study.
  • Presence of any disorder of the central nervous or psychiatric system that may hinder the participation of the patient in the study.

研究者

发起方
MGI PHARMA, INC.,

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