跳至主要内容
临床试验/NCT03877796
NCT03877796招募中不适用

Development of Drug Response Predictor (DRP) to Test Sensitivity to Investigational Anti-Cancer Drugs in Patients With Advanced Ovarian Cancer

Allarity Therapeutics13 个研究点 分布在 2 个国家目标入组 60 人开始时间: 2019年4月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
13
主要终点
Identification of ovarian cancer patients with high likelihood of being sensitive to investigational cancer drug

研究概览

简要总结

The patient's local archival tumor tissue (FFPE) from original tumor, or from the metastatic tissue, will be collected to potentially identify if they - at a later stage of their disease - will be likely to benefit from treatment with any of the investigational cancer drugs available to Allarity Therapeutics. Data from this study can further be used to explore in a retrospective fashion, sensitivity to other chemotherapeutic drugs previously used in the treatment of their ovarian cancer, to investigate whether or not the DRP® method can predict and confirm the obtained sensitivity to the prior given drugs as well as prospective analyses guiding the Investigators on future treatments.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

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

  • Patients with histological confirmed epithelia ovarian cancer
  • Patients must have platinum-resistant disease, defined as progression within 6 months after the last dose of platinum-based chemotherapy, or are platinum ineligible.
  • Patients have received no more than one prior line of therapy in the platinum resistant or platinum ineligible setting
  • FFPE tumor tissue available

排除标准

  • Patients who have platinum-refractory disease, defined as progression during the last platinum-based chemotherapy.
  • Other malignancy with exception of any stage I and II cancer that is deemed cured by the Investigator

研究组 & 干预措施

Ovarian cancer patients

with formalin-fixed paraffin-embedded (FFPE) tumor tissue available

干预措施: Drug Response Predictor® (DRP) (Device)

结局指标

主要结局

Identification of ovarian cancer patients with high likelihood of being sensitive to investigational cancer drug

时间窗: up to 2 years

based on FFPE ovarian cancer tissue

次要结局

  • Retrospective analysis of whether or not the DRP method can predict and confirm the obtained sensitivity to the prior drugs used in the treatment of ovarian cancer(up to 2 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (13)

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