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临床试验/NCT00043368
NCT00043368已完成2 期

A Continuation Study Of PF-3512676 (CPG 7909) Injection In Patients With Metastatic Or Recurrent Malignancies Who Have Stable Disease Or Who Have Responded To Pf-3512676 Injection Therapy

Pfizer1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2002年9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
已完成
发起方
Pfizer
入组人数
31
试验地点
1
主要终点
Adverse Events and DLTs will be evaluated by the Investigator and summarized.

研究概览

简要总结

This protocol allows patients who completed Coley oncology studies using PF-3512676 (CPG 7909) Injection to continue receiving the treatment until disease progression.

研究设计

研究类型
Interventional
分配方式
Non 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

  • Immediate (within 4 weeks) prior completion of a clinical trial of PF-3512676 Injection alone or in combination with other anti-neoplastic treatment for malignancy.

排除标准

  • The patient has received any anti-neoplastic therapy since completing a prior trial with PF-3512676 Injection, or has participated in another clinical trial following participation in a trial with PF-3512676 Injection.

研究组 & 干预措施

1

Experimental

Patients will be treated with the same dosing regimen and schedule of PF-3512676 Injection with which they were treated at the end of the previous PF-3512676 Injection trial. Any proposed changes to their schedule/regimen will be at the discretion of the treating physician, following consultation with Coley.

干预措施: PF-3512676 (Drug)

结局指标

主要结局

Adverse Events and DLTs will be evaluated by the Investigator and summarized.

时间窗: indeterminate

次要结局

  • No formal statistical analysis of this study will be conducted. All clinical data may be summarized and included in data listings.(indeterminate)

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (1)

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