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临床试验/JPRN-UMIN000003130
JPRN-UMIN000003130已完成3 期

Randomized Phase III Trail of Liposomal Doxorubicin(PLD)50mg/m2 versus Liposomal Doxorubicin(PLD)40mg/m2 in Patients with Platinum-Refractory and -Resistant Mullerian Carcinoma (Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Carcinoma). - Randomized Trial of PLD 50mg/m2 vs PLD 40mg/m2 for Platinum-Refractory and -Resistant Mullerian Carcinoma

Japanese Gynecologic Oncology Group0 个研究点目标入组 470 人开始时间: 2010年2月2日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
470

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
Female

入选标准

  • 未提供

排除标准

  • 1) Patients who have a history of hypersensitivity to Doxorubicin 2) Patients with active infection 3) Patients with severe complications (Heart disease, uncontrolled diabetes, malignant hypertension, or bleeding tendency) 4) Patients who have any other cancer within the past 5 years 5) Patients have myocardial infarction within 90 days or angina attack. 6) Patients who have treated prior chemotherapy with Anthracycline of a total dose of more than 250 mg/m2 doxorubicin 7) Patients have received prior PLD chemotherapy. 8) Patients have symptomatic brain metastasis with symptom. 9) Patients are pregnant or breast feeding. 10)Patients who are inappropriate to enter this study with any safety reasons,judged by the treating physician.

研究者

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