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临床试验/EUCTR2007-004043-30-HU
EUCTR2007-004043-30-HU进行中(未招募)不适用

A Phase III, Randomized, Double-Blind, Active-Controlled,Parallel-Group Study, Conducted Under In-House Blinding Conditions,to Examine the Safety, Tolerability, and Efficacy of aSingle Dose of Intravenous MK-0517 for the Prevention ofChemotherapy-Induced Nausea and Vomiting (CINV) AssociatedWith Cisplatin Chemotherapy - CINV Single Dose Study

Merck & Co., Inc.0 个研究点目标入组 2,292 人开始时间: 2007年12月12日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
2,292

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Female or male adult patients, greater than or equal 18 years of age. Patient is scheduled to receive his or her first course of cisplatin chemotherapy for a documented solid malignancy at a dose of greater than or equal 70 mg/m2. Patient has a Karnofsky score of greater than or equal 60. Patient is able to understand study procedures and agrees to participate in the study by giving written informed consent. Please see Protocol for complete list.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patient has symptomatic primary or metastatic CNS malignancy. Patient has received or is scheduled to receive radiation therapy to the abdomen or pelvis in the week prior to Treatment Day 1 through Day 6. Patient has vomited in the 24 hours prior to Treatment Day 1. Patient is to receive multiple-day chemotherapy with cisplatin in a single cycle. Patient is to receive chemotherapy of moderate or high emetogenicity (per Hesketh Classification of Emetogenic Chemotherapy Agents) during the 6 days prior to the cisplatin infusion and/or during the 6 days following cisplatin infusion. Chemotherapy agents with a classification of moderate or above can be given on the same day as cisplatin, and should be given following the cisplatin infusion. There is no restriction on the timing of administration of chemotherapeutic agents of low or minimal emetogenicity except for patients receiving taxanes or pemetrexed. Please see Protocol for complete list.

研究者

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