BENITIONSClinical Trial Intelligence

Cytarabine and Daunorubicin Hydrochloride in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia

第1相 完了 NCT02971397

対象疾患Acute Myeloid Leukemia
第1相
スポンサーWake Forest University Health Sciences
ステータス完了
参加者数40 名
介入(薬剤)Bone Marrow Aspiration and Biopsy, Cytarabine, Daunorubicin Hydrochloride, Laboratory Biomarker Analysis
開始日2016年11月
完了日2018年3月
結果公開日2026年3月23日

概要

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

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
Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy)2 events
Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy)3 events
Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy)1 events
Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy)2 events
Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy)2 events

Proportion of Patients Who Complete the Infusion Therapy

72 hours · Participants

Treatment (Cytarabine, Daunorubicin Hydrochloride, Biopsy)40 Participants

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同じ疾患の他の治験

すべての治験

このページは ClinicalTrials.gov の公開データをまとめたものです。医学的助言ではなく、投資助言でもありません。必ず専門医にご相談ください。