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临床试验/NCT01231347
NCT01231347已完成3 期

A Phase 3, Multicenter, Randomized, Double-Blind, Placebo Controlled, Trial of AMG 479 or Placebo in Combination With Gemcitabine as First Line Therapy for Metastatic Adenocarcinoma of the Pancreas

NantCell, Inc.1 个研究点 分布在 1 个国家目标入组 800 人开始时间: 2011年4月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
800
试验地点
1
主要终点
Determine if the Treatment of AMG 479 at 12 mg/kg and/or 20 mg/kg in Combination With Gemcitabine Improves Overall Survival as Compared With Placebo in Combination With Gemcitabine in Subjects With Metastatic Adenocarcinoma of the Pancreas

研究概览

简要总结

AMG 479 is an investigational fully human monoclonal antibody that targets type 1 insulin-like growth factor receptor (IGF-1R). Signaling through IGF-1R plays an important role in the regulation of cell growth and survival. The primary purpose of the study is to determine if AMG 479 and gemcitabine improves overall survival as compared to placebo and gemcitabine.

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
Triple (Participant, Care Provider, Investigator)

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

  • Untreated metastatic adenocarcinoma of the pancreas
  • Adequate hematologic, renal and liver function
  • Eastern Cooperative Oncology Group (ECOG) 0 or 1

排除标准

  • Prior chemotherapy or radiotherapy for pancreatic cancer
  • Central nervous system metastases
  • External biliary drain

研究组 & 干预措施

Placebo + gemcitabine

Placebo Comparator

Arm 1: AMG 479-placebo IV days 1 and 15 plus gemcitabine 1000 mg/m2 IV days 1, 8, and 15 of a 28 day cycle

干预措施: Placebo (Drug)

Placebo + gemcitabine

Placebo Comparator

Arm 1: AMG 479-placebo IV days 1 and 15 plus gemcitabine 1000 mg/m2 IV days 1, 8, and 15 of a 28 day cycle

干预措施: gemcitabine (Drug)

AMG 479 12 mg/kg dose + gemcitabine

Experimental

Arm 2: AMG 479 12 mg/kg IV days 1 and 15 plus gemcitabine 1000 mg/m2 IV days 1, 8, and 15 of a 28 day cycle

干预措施: AMG 479 (Drug)

AMG 479 12 mg/kg dose + gemcitabine

Experimental

Arm 2: AMG 479 12 mg/kg IV days 1 and 15 plus gemcitabine 1000 mg/m2 IV days 1, 8, and 15 of a 28 day cycle

干预措施: gemcitabine (Drug)

AMG 479 20 mg/kg + gemcitabine

Experimental

Arm 3: AMG 479 20 mg/kg IV days 1 and 15 plus gemcitabine 1000 mg/m2 IV days 1, 8, and 15 of a 28 day cycle

干预措施: AMG 479 (Drug)

AMG 479 20 mg/kg + gemcitabine

Experimental

Arm 3: AMG 479 20 mg/kg IV days 1 and 15 plus gemcitabine 1000 mg/m2 IV days 1, 8, and 15 of a 28 day cycle

干预措施: gemcitabine (Drug)

结局指标

主要结局

Determine if the Treatment of AMG 479 at 12 mg/kg and/or 20 mg/kg in Combination With Gemcitabine Improves Overall Survival as Compared With Placebo in Combination With Gemcitabine in Subjects With Metastatic Adenocarcinoma of the Pancreas

时间窗: From randomization up to 20 months

The primary endpoint of the study was OS, defined as the time from randomization to death.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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