跳至主要内容
临床试验/NCT00383331
NCT00383331终止2 期

A Phase II Study of ALIMTA® (Pemetrexed) and GEMZAR® (Gemcitabine) Every 14 Days Versus Pemetrexed and Gemcitabine Every 21 Days in Advanced Non-Small Cell Lung Cancer

Eli Lilly and Company1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2007年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
19
试验地点
1
主要终点
Best Overall Tumor Response

研究概览

简要总结

This study is designed to evaluate Pemetrexed and Gemcitabine Day 1 followed by Gemcitabine Day 8 every 21 days (Arm A) and Pemetrexed and Gemcitabine Day 1 every 14 days (Arm B) in patients with NSCLC. Each agent and sequence has well demonstrated antitumor activity respectively in patients with locally advanced or metastatic NSCLC. Therefore, it is reasonable to investigate the most optimal schedule for this combination, and which combination is associated with the most anti-tumor activity in the phase II arena.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • histologic or cytologic diagnosis of NSCLC Stage IIIB or IV
  • no prior systemic chemotherapy for advanced Non-Small Cell Lung Cancer
  • Prior radiotherapy must be completed at least 4 weeks before study enrollment.

排除标准

  • estimated life expectancy of 12 weeks
  • a serious cardiac condition, such as myocardial infarction within 6 months, angina, or heart disease
  • documented brain metastases unless the patient has completed successful local therapy for central nervous system metastases and has been off of corticosteroids for at least 2 weeks before enrollment
  • significant weight loss (that is, > 10%) over the previous 6 weeks before study entry.

研究组 & 干预措施

A

Experimental

干预措施: Pemetrexed (Drug)

A

Experimental

干预措施: Gemcitabine (Drug)

B

Experimental

干预措施: Pemetrexed (Drug)

B

Experimental

干预措施: Gemcitabine (Drug)

结局指标

主要结局

Best Overall Tumor Response

时间窗: baseline and every 14 or 21 day cycle (6-9 cycles), every 6 weeks post-therapy follow-up

Best response recorded from the start of treatment until disease progression/recurrence using Response Evaluation Criteria In Solid Tumors (RECIST) criteria that defines when participants improve ("respond"), stay the same ("stable"), or worsen ("progression") during treatment.

次要结局

  • Progression Free Survival(baseline and every 14 or 21 day cycle (6-9 cycles), every 6 weeks post-therapy follow-up)
  • Time to Progressive Disease(baseline and every 14 or 21 day cycle (6-9 cycles), every 6 weeks post-therapy follow-up)
  • Duration of Response(baseline and every 14 or 21 day cycle (6-9 cycles), every 6 weeks post-therapy follow-up)
  • Time to Treatment Failure(baseline and every 14 or 21 day cycle (6-9 cycles), every 6 weeks post-therapy follow-up)
  • Overall Survival(baseline and every 14 or 21 day cycle (6-9 cycles), every 6 weeks post-therapy follow-up)

研究者

申办方类型
Industry

研究点 (1)

Loading locations...

相似试验