跳至主要内容
临床试验/PER-018-04
PER-018-04已完成未知

An open, randomized, international, multicenter, phase III study of Capecitabine (Xeloda®) in combination with cisplatin versus 5-FU / cisplatin in patients with advanced and / or metastatic gastric cancer.

PRODUCTOS ROCHE Q.F.S.A.,0 个研究点目标入组 0 人开始时间: 2004年5月3日最近更新:

试验速览

阶段
未知
状态
已完成
发起方

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
0 至 0(—)

入选标准

  • Adults 18 to 75 years of age
  • Advanced and/or metastatic gastric cancer with at least 1 measurable lesion

排除标准

  • Uncontrolled infection
  • Evidence of central nervous system (CNS) metastases
  • History of other malignancy within the last 5 years, except cured basal cell cancer of the skin or cured in-situ cancer of the uterine cervix
  • Radiation therapy or major surgery within 4 weeks of study drug
  • Previous chemotherapy

研究者

发起方
PRODUCTOS ROCHE Q.F.S.A.,

相似试验

进行中(未招募)
不适用
An international, multicenter, randomized, open-label, safety andefficacy trial of intravenous zoledronic acid administered eitheronce or twice yearly in children with severe osteogenesisimperfecta, a 1-year extension to CZOL446H2202 - 2202EOsteogenesis Imperfecta
EUCTR2004-001666-40-HUovartis Pharma AG130
进行中(未招募)
不适用
Bisphosphonate Treatment of Osteogenesis ImperfectaOsteogenesis Imperfecta
EUCTR2015-003539-37-Outside-EU/EEAovartis158
进行中(未招募)
1 期
An international, multicenter, randomized, open-label, safety andefficacy trial of intravenous zoledronic acid administered eitheronce or twice yearly in children with severe osteogenesisimperfecta, a 1-year extension to CZOL446H2202 - 2202EOsteogenesis Imperfecta
EUCTR2004-001666-40-BEovartis Pharma AG130
进行中(未招募)
不适用
An international, multicenter, randomized, open-label, safety andefficacy trial of intravenous zoledronic acid administered eitheronce or twice yearly in children with severe osteogenesisimperfecta, a 1-year extension to CZOL446H2202 - 2202EOsteogenesis Imperfecta
EUCTR2004-001666-40-GBovartis Pharma AG130
进行中(未招募)
不适用
A Randomized, international, multi-center, open-label study to document pharmacokinetics and optimal timing of initiation of dronedarone TreatmEnt following long-term aMIodarone in patients with paroxysmal or perSistent Atrial Fibrillation whatever the reason for the change of treatment - ARTEMIS AF Long-TermParoxysmal or persistent atrial fibrillationMedDRA version: 14.1Level: PTClassification code 10003658Term: Atrial fibrillationSystem Organ Class: 10007541 - Cardiac disorders
EUCTR2010-019247-19-DKsanofi aventis groupe105