NL-OMON54399招募中4 期
Pharmacokinetic boosting of olaparib to improve exposure, tolerance and cost-effectiveness (PROACTIVE-study) - PROACTIVE
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 160
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
- 18 至 99(—)
入选标准
- •Part A - proof of concept
- •Subjects who start or are on treatment with olaparib tablets, according to
- •the drug label and physician*s discretion;
- •Subjects who are able and willing to provide written informed consent prior
- •to screening;
- •Age of 18 years or older;
- •Able to measure the outcome of the study in this subject (e.g. patient
- •availability; willing and being able to undergo repeated plasma sample
- •collection);
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
- •Part B - clinical evaluation
- •Subjects who start on treatment with olaparib tablets, according to the drug
- •label and physician*s discretion;
- •Subjects who are able and willing to provide written informed consent prior
- •to screening;
- •Age of 18 years or older;
- •Able to measure the outcome of the study in this subject (e.g. patient
- •availability; willing and being able to undergo sample collection for PK and PD
- •Expected to be on olaparib treatment for >= 3 months;
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0-3.
排除标准
- •Part A + B
- •Concurrent use of other anti-cancer therapies;
- •Concurrent use of potent inducers or inhibitors of CYP3A4 as assessed with
- •the KNMP *G-standaard*;
- •Known contra-indications for treatment with cobicistat in line with the
- •summary of product characteristics;
研究者
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