Safety and Efficacy Study of Idarubicin Dose Intensification to Treat Acute Myeloid Leukemia

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

49

Participants

Timeline

Start Date

July 31, 2011

Primary Completion Date

March 31, 2025

Study Completion Date

March 31, 2025

Conditions
Leukemia, Myeloid, Acute
Interventions
DRUG

Idarubicin

"In the phase I study, idarubicin dose is increased step by step as follows: 12 mg/m2/day for 3 days IV in the 1st step; 15 mg/m2/day for 3 days IV in the 2nd step; 18 mg/m2/day for 3 days IV in the 3rd step.~In the phase II study, idarubicin dose is the maximum tolerated dose that is determined from the phase I study or 18 mg/m2/day for 3 days ."

Trial Locations (1)

143-729

Division of Hematology-Oncology, Konkuk University Medical Center, Seoul

All Listed Sponsors
collaborator

Chung-Ang University Hosptial, Chung-Ang University College of Medicine

OTHER

collaborator

Seoul National University Hospital

OTHER

collaborator

Ewha Womans University

OTHER

collaborator

Samsung Medical Center

OTHER

collaborator

Chonbuk National University Hospital

OTHER

collaborator

Pusan National University Hospital

OTHER

collaborator

Hanyang University Seoul Hospital

OTHER

collaborator

Soon Chun Hyang University

OTHER

lead

Konkuk University Medical Center

OTHER

NCT01518556 - Safety and Efficacy Study of Idarubicin Dose Intensification to Treat Acute Myeloid Leukemia | Biotech Hunter | Biotech Hunter