Overview

CHIP-AML22/Quizartinib: Quizartinib + Chemotherapy in Newly Diagnosed Pediatric FLT3-ITD+ and NPM1wt AML Patients

Status:
RECRUITING
Trial end date:
2032-06-01
Target enrollment:
Participant gender:
Summary
The CHIP-AML22 Master protocol has the overall aim of increasing the cure rate in newly diagnosed pediatric de novo AML patients, while avoiding unnecessary toxicity. The linked Quizartinib trial (CHIP-AML22/Quizartinib) is a phase II, single arm, open label, study on the safety, efficacy, pharmacokinetics and pharmacodynamics of quizartinib in combination with chemotherapy and as single-agent after high dose therapy in newly diagnosed pediatric AML patients with a FLT3-ITD mutation and NPM1 wild-type.
Phase:
PHASE2
Details
Lead Sponsor:
Princess Maxima Center for Pediatric Oncology
Collaborator:
Daiichi Sankyo
Treatments:
Cytarabine
Daunorubicin
Dexrazoxane
Etoposide
fludarabine
Methotrexate
Mitoxantrone
quizartinib