BENITIONSClinical Trial Intelligence

Phase 3 Trial of Blinatumomab vs Standard Chemotherapy in Pediatric Subjects With HIgh-Risk (HR) First Relapse B-precursor Acute Lymphoblastic Leukemia (ALL)

3期 已完成 NCT02393859

适应症Leukemia, Acute Lymphoblastic
分期3期
申办方Amgen
状态已完成
受试者人数111 人
干预(药物)Blinatumomab, Dexamethasone, Vincrisitne, Daunorubicin, Methotrexate
开始日期2015年11月10日
完成日期2019年7月17日
结果公布日2020年7月13日

摘要

B-precursor ALL is an aggressive malignant disease. Therapy is usually stratified according to risk characteristics to ensure that appropriate treatment is administered to patients with high-risk of relapse. In general, pediatric treatment regimens are more intense than those employed in adults and include courses of combination chemotherapy. Standard of care chemotherapy is associated with considerable toxicity. There is a lack of novel treatment options for subjects who relapse or are refractory to treatment. Therefore, innovative therapeutic approaches are urgently needed. Blinatumomab is a bispecific single-chain antibody construct designed to link B cells and T cells resulting in T cell activation and a cytotoxic T cell response against CD19 expressing cells. This study will evaluate the event-free survival (EFS) after treatment with blinatumomab when compared to standard of care (SOC) chemotherapy. The effect of blinatumomab on overall survival and reduction of minimal residual disease compared to SOC chemotherapy will also be investigated.

Kaplan Meier Estimate: Event-Free Survival (EFS; Primary Analysis)

As of the primary analysis data cutoff date (17 July 2019), overall median follow-up time for EFS was 22.4 months. · months

HC3 Chemotherapy7.4 months
BlinatumomabNA months
p-value< 0.001
Normal score-11.54

Kaplan Meier Estimate: EFS (Final Analysis)

At final analysis, overall median follow-up time for EFS was 51.9 months. · months

HC3 Chemotherapy7.8 months
BlinatumomabNA months
p-value< 0.001
Normal score-13.90

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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。