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临床试验/NCT03054909
NCT03054909已完成2 期

QUILT-2.021: Randomized Study of Single Course of Intraperitoneal (IP) ALT-803 Followed by Subcutaneous (SQ) Maintenance ALT-803 Versus Subcutaneous (SQ) Maintenance ALT-803 Only After 1st Line Chemotherapy for Advanced Ovarian, Fallopian Tube, and Primary Peritoneal Cancer

Masonic Cancer Center, University of Minnesota2 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2017年9月19日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
7
试验地点
2
主要终点
Progression Free Survival

研究概览

简要总结

This is a single center, randomized phase II study of an IL-15Rα-Fc super-agonist complex (ALT-803) given as maintenance therapy after the completion of 1st line IV/IP chemotherapy for the treatment of advanced ovarian, fallopian tube, and primary peritoneal cancer.

详细描述

In this study all patients receive four 8 week cycles of ALT-803 consisting of 4 weekly doses followed by a 4 week rest (no treatment). As it is not known how intraperitoneal (IP) administration (a route of drug administration frequently used for gynecologic cancers) of ALT-803 compares to subcutaneous (SQ) administration, both routes of administration will be tested. The primary objective of this trial is to select one method of delivery for further testing.

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
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Progression Free Survival

时间窗: 6 months

Incidence of Progression Free Survival after first treatment of ALT-803.

次要结局

  • Overall Survival(2 year)
  • ALT-803 Associated Toxicities(1 year)
  • Progression Free Survival(2 years)
  • Incidence of Recorded Toxicity Grade 3 or Greater(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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