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临床试验/JPRN-UMIN000015877
JPRN-UMIN000015877已完成1 期

PhaseI/II study of irinotecan and oxaliplatin combination chemotherapy in patients with gemcitabine and 5-fluorouracil refractory pancreatic cancer. - PhaseI/II study of IROX therapy in gemcitabine and 5-fluorouracil refractory pancreatic cancer.

Chiba cancer center0 个研究点目标入组 30 人开始时间: 2014年12月10日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
30

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 79years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1)Severe complications. (2)Grade2 or greater peripheral neuropathy. (3)Patients who received blood transfusions or hematopoietic growth factors within 7 days before the laboratory test (4)Active infections. (5)Pulmonary fibrosis or interstitial pneumonia. (6)Clinically evident pleural, abdominal or cardiac effusion. (7)Watery diarrhea within 3days before registration. (8)Surgery within 4weeks,chemotherapy within 2 weeks,radiation therapy within 2 weeks. (9)Has unresolved toxicity of greater than or equal to CTCAE Grade 2 attributed to any prior therapies. (10)Poorly controlled diabetes. (11)Brain metastasis. (12)Severe mental disorder. (13)Double advanced cancer. (14)Severe drug allergies. (15)pregnant or lactating female. (16)Current use atazanavir. (17)Concurrent chronic systemic steroid treatment. (18)Having UGT1A1*6/*6,UGT1A1*28/*28 or UGT1A1*6/*28 gene (19)Prior therapy with irinotecan or oxaliplatin. (20)Inappropriate for entry onto the study,as diagnosed by primary physician.

研究者

发起方
Chiba cancer center

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