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临床试验/NCT00787033
NCT00787033已完成1 期

A Phase 1, Open-Label, Dose Escalation Study To Evaluate Safety, Pharmacokinetics And Pharmacodynamics Of PF-04554878 In Patients With Advanced Non-Hematologic Malignancies

Verastem, Inc.1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2008年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
46
试验地点
1
主要终点
Recommended Phase 2 Dose

研究概览

简要总结

Phase 1 safety, pharmacokinetics, and pharmacodynamics trial of the focal adhesion kinase (FAK) inhibitor PF-04554878 in patients with advanced non-hematologic malignancies, including patients with malignancies appropriate for serial biopsy. Screening consists of medical history, physical examination ECOG performance status, blood draws, a pregnancy test for female patients of childbearing potential, a FDG-PET and tumor imaging. Treatment consists of PF-04554878 pills continued until progression of disease, unacceptable toxicity, or patient request. Evaluations for bioactivity are measured by serial FDG-PET and blood tests for biomarkers related to FAK and Pyk2 activities.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Patients with advanced non-hematologic malignancies.
  • Adequate organ function, including bilirubin less than 1.5 x ULN, and ECOG (Eastern Cooperative Oncology Group) performance status of 0-2.

排除标准

  • Clinically significant gastrointestinal abnormalities, requirement for systemic anticoagulants or potent CYP 2C8 inhibitors, and history of clinically significant cardiac or pulmonary disorders

研究组 & 干预措施

1

Experimental

Dose escalation study with Expansion Cohorts at RP2D and Schedule

干预措施: PF-04554878 (Drug)

结局指标

主要结局

Recommended Phase 2 Dose

时间窗: 18 months

Overall safety profile of PF-04554878, including Dose-Limiting Toxicity (DLT)

时间窗: 18 months

次要结局

  • Tumor metabolic response(18 months)
  • FAK-related biomarkers in tumor biopsies and blood(18 months)
  • Molecular profiling (genomics data) based on the optional studies with whole blood and/or tumor samples(18 months)
  • PF-04554878 pharmacokinetic (PK) parameters and Midazolam PK parameters(18 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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