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Clinical Trial Summary

The primary objective of this study is to evaluate the efficacy of moxetumomab pasudotox in pediatric subjects with relapsed or refractory B-cell ALL or B-cell lymphoblastic lymphoma


Clinical Trial Description

This is a global, multicenter, open-label, single-arm Phase 2 study to evaluate the efficacy and safety of moxetumomab pasudotox monotherapy in pediatric subjects with relapsed or refractory B-cell ALL or B-cell lymphoblastic lymphoma. Subjects will be enrolled at sites in North America, Europe, and Australia. This is an approximate 35-month study. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02227108
Study type Interventional
Source MedImmune LLC
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Status Terminated
Phase Phase 2
Start date August 2014
Completion date November 2015