Testing the Combination of the Study Drugs Cediranib and Olaparib in Recurrent Ovarian Cancer
第2相
実施中(募集終了)
NCT02345265
| 対象疾患 | Fallopian Tube Carcinoma, Fallopian Tube Endometrioid Adenocarcinoma, Fallopian Tube Serous Adenocarcinoma, Ovarian Carcinoma |
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| 相 | 第2相 |
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| スポンサー | National Cancer Institute (NCI) |
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| ステータス | 実施中(募集終了) |
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| 参加者数 | 70 名 |
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| 介入(薬剤) | Biopsy Procedure, Biospecimen Collection, Cediranib Maleate, Computed Tomography, Echocardiography Test |
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| 開始日 | 2016年5月23日 |
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| 完了日 | 2022年7月7日 |
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| 結果公開日 | 2023年3月28日 |
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概要
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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