Cytarabine and Daunorubicin Hydrochloride in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia
1期
已完成
NCT02971397
| 适应症 | Acute Myeloid Leukemia |
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| 分期 | 1期 |
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| 申办方 | Wake Forest University Health Sciences |
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| 状态 | 已完成 |
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| 受试者人数 | 40 人 |
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| 干预(药物) | Bone Marrow Aspiration and Biopsy, Cytarabine, Daunorubicin Hydrochloride, Laboratory Biomarker Analysis |
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| 开始日期 | 2016年11月 |
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| 完成日期 | 2018年3月 |
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| 结果公布日 | 2026年3月23日 |
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摘要
This pilot clinical trial studies the side effects of cytarabine and daunorubicin hydrochloride and to see how well they work in treating patients with newly diagnosed acute myeloid leukemia. Drugs used in chemotherapy, such as cytarabine and daunorubicin hydrochloride, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading, and may be safer for the heart.
Number of Participants With Cardiac Toxicity, Defined as Reduction in LVEF of >= 10% Compared to Baseline LVEF and EF =< 50% on the Follow-up Scan, Assessed Using MRI
Baseline up to 3 months · Participants
| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 3 Participants |
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Unexpected Toxicities (Exclude Hematologic and Infectious) ≥ Grade 3, as Measured by CTCAE v 4.0
Up to 30 days after last dose of study drug · events
| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 3 events |
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| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 2 events |
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| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 3 events |
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| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 1 events |
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| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 2 events |
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| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 2 events |
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Proportion of Patients Who Complete the Infusion Therapy
72 hours · Participants
| Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy) | 40 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。