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临床试验/JPRN-UMIN000006911
JPRN-UMIN000006911招募中2 期

Randomized Phase II study of Bevacizumab with SOX versus Bevacizumab with XELOX as second-line therapy in metastatic colorectal cancer which has prior therapy of S-1 and CPT-11 - Randomized Phase II study of Bevacizumab with SOX versus Bevacizumab with XELOX as second-line therapy in metastatic colorectal cancer which has prior therapy of S-1 and CPT-11

Tsuchiura kyodo general hospital0 个研究点目标入组 60 人开始时间: 2011年12月19日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
60

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) History of severe allergy (2) Pregnant or lactating women or women of childbearing potential (3) Severe infectious disease (4) Serious complication (e.g. interstitial pneumonia or pulmonary fibrosis, kidney injury, hepatic failure, uncontrolled diabetes mellitus, uncontrolled hypertension) (5) Comorbidity or history of heart failure (6) Peptic ulcers (7) Peripheral neuropathy (8) Severe diarrhea (9) Massive ascites or pleural effusion requiring treatment (10) Metastasis to the CNS (11) Current or previous (within the last 6 months) history of GI perforation (12) Previous history of thromboembolism, cerebral infarction, pulmonary infarction, interstitial pneumonia or hemoptysis (=> 2.5ml) (13) Any surgical treatments within 28 days (14) Evidence of bleeding diathesis or coagulopathy (15) Ongoing treatment with anticoagulant or aspirin (> 325mg/day) (16) Synchronous or metachronous (within 5 years) malignancy other than carcinoma in situ (17) Under coutinuous steroid administration (18) Administration contraindication of L-OHP, Bevacizumab, S-1 or Capecitabine (19) Presence of severe colorectal stricture (20) Any other cases who are regarded as inadequate for study enrollment by the investigator

研究者

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