drugset / Trial / NCT02393859

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

NCT02393859

Phase 3 Completed 111 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

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.

Timeline

Start
2015-11-10
Primary completion
2019-07-17
Completion
2022-11-21

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Blinatumomab Monoclonal antibody 15 ug/m2 Intravenous
Comparator Daunorubicin Small molecule 30 mg/m2 Intravenous
Comparator Dexamethasone Small molecule 10 mg/m2 Intravenous
Comparator Ifosfamide Small molecule 800 mg/m2 Intravenous
Comparator Methotrexate Small molecule 1 g Intravenous
Comparator Pegaspargase Protein / enzyme biologic 1000 unknown Intravenous
Comparator Vincrisitne Unknown 1.5 mg/m2 Intravenous
Comparator Asparaginase Erwinia chrysanthemi Protein / enzyme biologic 20000 unknown Intravenous