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临床试验/NCT00499291
NCT00499291撤回不适用

Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Study of Nab-Paclitaxel (Nanoparticle Albumin Bound-Paclitaxel) in Patients With Advanced Solid Tumors

Eastern Cooperative Oncology Group0 个研究点开始时间: 2006年9月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
撤回
主要终点
Inter-individual pharmacokinetic variability

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as paclitaxel albumin-stabilized nanoparticle formulation, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

PURPOSE: This clinical trial is studying how well paclitaxel albumin-stabilized nanoparticle formulation works in treating patients with advanced or refractory solid tumors.

详细描述

OBJECTIVES:

Primary

  • To develop a population pharmacokinetic model for paclitaxel administered as paclitaxel albumin-stabilized nanoparticle formulation (nab-paclitaxel) to a large population of patients with advanced or refractory cancer to characterize the inter-individual pharmacokinetic variability of this agent.

Secondary

  • To explore nab-paclitaxel pharmacokinetic parameters in patients with metastatic prostate cancer (castrate), metastatic breast cancer, advanced non-small cell lung cancer and other incurable advanced or refractory tumors amenable to treatment with nab-paclitaxel.
  • To explore the association between exposure to total and unbound paclitaxel after administration of nab-paclitaxel and neutropenia.
  • To explore the association between the CYP2C8*3 variant and paclitaxel clearance.
  • To explore the association between other variants of CYP2C8 and other genes involved in paclitaxel disposition including CYP3A4, CYP3A5, SLCO1B3 (OATP8), and ABCB1 (MDR1) and paclitaxel pharmacokinetic parameters and toxicity after one course of treatment.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Inter-individual pharmacokinetic variability

次要结局

  • Pharmacokinetic parameters
  • Neutropenia
  • CYP2C8*3 variant expression
  • Genetic variance relating to pharmacokinetics and toxicity

研究者

申办方类型
Network
责任方
Sponsor

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