Carboplatin, Gemcitabine Hydrochloride, and Berzosertib in Treating Patients With Recurrent and Metastatic Ovarian, Primary Peritoneal, or Fallopian Tube Cancer
第1相
実施中(募集終了)
NCT02627443
| 対象疾患 | Metastatic Fallopian Tube Carcinoma, Metastatic Ovarian Carcinoma, Metastatic Primary Peritoneal Carcinoma, Ovarian Endometrioid Tumor |
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| 相 | 第1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 | 35 名 |
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| 介入(薬剤) | Berzosertib, Carboplatin, Gemcitabine Hydrochloride, Laboratory Biomarker Analysis, Pharmacological Study |
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| 開始日 | 2017年5月16日 |
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| 完了日 | 2024年10月4日 |
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| 結果公開日 | 2026年4月2日 |
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概要
This phase I trial studies the side effects and best dose of gemcitabine hydrochloride and berzosertib when given together with carboplatin in treating patients with ovarian, primary peritoneal, or fallopian tube cancer that has come back (recurrent) and has spread to other places in the body (metastatic). Chemotherapy drugs, such as carboplatin and gemcitabine hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Berzosertib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving berzosertib with chemotherapy (carboplatin and gemcitabine hydrochloride) may work better in treating patients with ovarian, primary peritoneal, or fallopian tube cancer compared to chemotherapy alone.
Dost Limiting Toxicity (DLT) (Phase I Dose Escalation)
Up to 28 days · Participants
| Dose Level 1 | 1 Participants |
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| Dose Level 2 | 2 Participants |
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Incidence of Adverse Events
Up to 3 years · Participants
| Dose Level 1 | 28 Participants |
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| Dose Level 2 | 5 Participants |
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| Dose Level 1 | 18 Participants |
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| Dose Level 2 | 4 Participants |
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| Dose Level 1 | 0 Participants |
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| Dose Level 2 | 0 Participants |
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