A PHASE 1/2, MULTI-CENTER, DOSE-ESCALATING STUDY TO EVALUATE THE SAFETY, PHARMACOKINETICS, PHARMACODYNAMICS, AND EFFICACY OF QUIZARTINIB ADMINISTERED IN COMBINATION WITH RE-INDUCTION CHEMOTHERAPY, AND AS A SINGLE-AGENT CONTINUATION THERAPY, IN PEDIATRIC RELAPSED/REFRACTORY AML SUBJECTS AGED 1 MONTH TO < 18 YEARS (AND YOUNG ADULTS AGED UP TO 21 YEARS) WITH FLT3-ITD MUTATIONS

Registry ID
AC220-A-U202
Source registry
HEALTH_CANADA
Status
Ongoing
Phase
PHASE1
Study type
INTERVENTIONAL
Sponsor
DAIICHI SANKYO INC
Start date
2020-03-06
Last update
2019-10-11

Conditions

Related clinical trials

View on source registry