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临床试验/JPRN-UMIN000017079
JPRN-UMIN000017079已完成1 期

Phase II Clinical Trial of Monotherapy with Irinotecan Hydrochloride (CPT-11) for Advanced or Recurrent Endometrial Cancer - Irinotecan For Endometrial Cancer

Kurume University0 个研究点目标入组 26 人开始时间: 2015年4月13日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
26

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
20years-old 至 75years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1.Patients with a history of treatment with topoisomerase I inhibitors (irinotecan, nogitecan, etc.) 2.Patients with liver dysfunction (jaundice) or serious renal dysfunction 3.Patients with serious drug allergies (hypersensitivity) 4.Patients with active double cancers 5.Patients who have or are suspected to have clinically problematic infections 6.Patients with poorly controlled hypertension or diabetes mellitus 7.Patients who have marked electrocardiographic abnormalities or clinically problematic cardiac disease 8.Patients with severe pulmonary disease (interstitial pneumonia, pulmonary fibrosis, severe pulmonary emphysema, etc.) 9.Patients with a history of clinically problematic mental disorders, central nervous system disorders, or cerebrovascular/cranial nerve disease 10. Patients with fresh gastrointestinal bleeding, intestinal paralysis, intestinal obstruction, or peptic ulcer 11.Patients with pleural effusion, ascites, or pericardial effusion requiring removal with the use of a drain 12.Patients with brain metastasis or who are suspected to have brain metastasis on the basis of clinical symptoms 13.Patients with diarrhea (watery stool) 14.Patients who are receiving atazanavir sulfate 15.Patients who are continuously receiving systemic administration of steroids (oral or intravenous infusion) 16.Pregnant women, breast-feeding women, or women who may (want to) become pregnant 17.Patients who are considered ineligible for participation in the study by the physician responsible (partially responsible) for treatment

研究者

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