Testing the Combination of the Study Drugs Cediranib and Olaparib in Recurrent Ovarian Cancer
2期
进行中(已停止招募)
NCT02345265
| 适应症 | Fallopian Tube Carcinoma, Fallopian Tube Endometrioid Adenocarcinoma, Fallopian Tube Serous Adenocarcinoma, Ovarian Carcinoma |
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| 分期 | 2期 |
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| 申办方 | National Cancer Institute (NCI) |
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| 状态 | 进行中(已停止招募) |
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| 受试者人数 | 70 人 |
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| 干预(药物) | Biopsy Procedure, Biospecimen Collection, Cediranib Maleate, Computed Tomography, Echocardiography Test |
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| 开始日期 | 2016年5月23日 |
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| 完成日期 | 2022年7月7日 |
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| 结果公布日 | 2023年3月28日 |
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摘要
This phase II trial studies how well olaparib and cediranib maleate work in treating patients with ovarian, primary peritoneal, or fallopian tube cancer that has come back after a period of improvement (recurrent). Olaparib and cediranib maleate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.
Progression-Free Survival (PFS) by HRR Status in Platinum-Sensitive Ovarian Cancer
Interval from start of treatment to documented disease progression per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 or death from any cause, whichever occurs first, assessed up to 32 months. · months
| HRRmt | 16.79 months |
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| HRRwt | 16.43 months |
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Objective Response Rate (ORR) in Platinum-Resistant Ovarian Cancer
Up to 32 months · percentage of participants
| Platinum-Resistant Ovarian Cancer | 22.86 percentage of participants |
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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。