drugset / Trial / NCT04521231

A Study of Subcutaneous Blinatumomab Administration in Participants With R/R and MRD+ B-ALL

NCT04521231

Phase 1/2 Active not recruiting 181 enrolled Amgen BeOne Medicines · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

The Phase I part of the study aims to evaluate the safety, efficacy, and tolerability of subcutaneous (SC) blinatumomab for treatment of Relapsed or Refractory B cell Precursor Acute Lymphoblastic Leukemia (R/R B-ALL), to determine the maximum tolerated dose (MTD), and recommended phase 2 dose(s) (RP2D) of SC administered blinatumomab. The Phase II part of the study will evaluate the safety, efficacy, and tolerability of SC blinatumomab for treatment of R/R B-ALL and Minimum Residual Disease Positive (MRD+) B-ALL in participants 12 years old and greater. It will also conduct a clinical pharmacokinetic (PK) evaluation of SC1 and SC2 blinatumomab formulations.

Timeline

Start
2021-01-04
Primary completion
2027-11-24
Completion
2029-05-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Blinatumomab Monoclonal antibody Subcutaneous