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临床试验/JPRN-UMIN000010254
JPRN-UMIN000010254已完成未知

Phase 1 study of sulfapyridine in patients with advanced gastric cancer. - SASP

ational Cancer Center Hospital East0 个研究点目标入组 6 人开始时间: 2013年3月31日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
6

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 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Chemotherapy, radiation therapy or other investigational drugs within 2 weeks prior to enrollment. 2) Active bleeding. 3) Patient with any of the following symptoms within 6 months prior to administration of the drug; myocardial infarction, severe or unstable angina, congested heart failure, cerebrovascular accident containing transient ischemic attack or pulmonary embolism. 4) Uncontrolled bronchial asthma. 5) Patient with brain metastases. 6) Laparotomy or thoracotomy within 4 weeks to enrollment. 7) Known hypersensitivity to sulfa drugs or acetylsalicylic acid formulation. 8) Women during pregnancy or lactation, women suspected of being pregnant, women desiring future fertility. 9) Patient is judged by the investigator to be inappropriate for study participation for any reason. 10) Patient with Ulcerative colitis, or treated patient with sulfapyridine or 5-ASA derivative.

研究者

发起方
ational Cancer Center Hospital East

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