跳至主要内容
临床试验/NCT01478308
NCT01478308撤回2 期

Metformin With Standard Taxotere and Prednisone in the Treatment of Castration Resistant Prostate Cancer

New Mexico Cancer Research Alliance0 个研究点开始时间: 2011年6月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
撤回
主要终点
Measure efficacy

研究概览

简要总结

This study is being conducted to determine the effectiveness of standard 3 weekly treatments using docetaxel and prednisone with metformin in patients with castration-resistant metastatic prostate cancer.

It is also being conducted to determine the levels of toxicity of metformin when added to every 3 weekly docetaxel treatments in patients with endocrine resistent, metastatic prostate cancer.

详细描述

This is a single-arm, non-randomized Phase II trial of docetaxel given every 3 weeks with metformin twice daily and Prednisone twice daily. The study duration of this trial is open ended. The patient would take the metformin only for as long as they are treated with docetaxel.

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
Male
接受健康志愿者

入选标准

  • All patients, 18 of age or older, with hormone refractory prostate cancer are eligible.
  • Patients must have a life expectancy of at least 12 weeks.
  • Patients must have a Zubrod performance status of 0-
  • Patients must sign an informed consent.
  • Patients should have adequate bone marrow function defined by an absolute peripheral granulocyte count of > 1,500 or cells/mm3 and platelet count >100,000/mm3 and absence of a regular red blood cell transfusion requirement.
  • Patients should have adequate hepatic function with a total bilirubin < 2 mg/dl and SGOT or SGPT < two times the upper limit of normal, and adequate renal function as defined by a serum creatinine < 1.5 x upper limit of normal.
  • Patients must have pathologically confirmed prostate cancer with PSA increasing despite androgen deprivation therapy.
  • Diabetic patients on therapy with Metformin are eligible provided that their Metformin dose is at least 850mg twice daily.

排除标准

  • Patients with symptomatic brain metastases are excluded from this study.
  • Patients on insulin are not eligible.
  • Patients may receive no other concurrent chemotherapy or radiation therapy during this trial.
  • Patients with severe medical problems such as uncontrolled diabetes mellitus, cardiovascular disease, and congestive heart failure defined as New York Heart Association Class III or IV, hepatic dysfunction, or active infections are not eligible for this trial.

结局指标

主要结局

Measure efficacy

时间窗: 7 years

To determine the antitumor activity of metformin in combination with docetaxel and prednisone which are considered standard of care administered to patients with hormone refractory prostate cancer.

次要结局

  • Measure toxicity(7 years)

研究者

申办方类型
Other
责任方
Sponsor

相似试验

Metformin With Standard Taxotere and Prednisone in... | 临床试验