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临床试验/NCT01668108
NCT01668108已完成不适用

Open, Multicenter Observational Study of Paclitaxel Utilized in Mono- or Combination Therapy for the Treatment of Breast Cancer, Non-small Cell Lung Cancer and Ovarial Cancer.

Onkovis GmbH1 个研究点 分布在 1 个国家目标入组 770 人开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Onkovis GmbH
入组人数
770
试验地点
1
主要终点
the quantity of Paclitaxel onkovis needed pro treatment cycle

研究概览

简要总结

The main purpose of this observational study with Paclitaxel is to determine the number of treatment cycles and the quantity of Paclitaxel onkovis needed therefore under the special circumstance of ambulant chemotherapy.

onkovis aims an economical utilization of the chemotherapeutics.The provision with adapted packaging sizes as to decrease the excess quantity to be discarded follows also this objective.

Secondary objectives are the survey of the side effects of Paclitaxel onkovis in comparison to Docetaxel. To this purpose, data regarding co medications and adverse events are also collected.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Indication for Paclitaxel according to the SmPC and treating physician

排除标准

  • according to the Paclitaxel SmPC

结局指标

主要结局

the quantity of Paclitaxel onkovis needed pro treatment cycle

时间窗: the time the participants will be followed depends on the number of treatment cycles; that means the time frame may extend up to 24 weeks (8 cycles).

Determine the quantity of Paclitaxel onkovis needed pro treatment cycle

次要结局

  • adverse events during and after treatment in comparison to Docetaxel onkovis(up to 24 weeks (8 cycles))

研究者

发起方
Onkovis GmbH
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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