Clinical Study of CWP232291 in Acute Myeloid Leukemia Patients

PHASE1/PHASE2UnknownINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

February 6, 2017

Primary Completion Date

October 31, 2022

Study Completion Date

October 31, 2022

Conditions
Acute Myeloid Leukemia
Interventions
DRUG

CWP232291

"For cohort 1-3, a fixed dose of ara-C at 1 G/m2 will be administered IV over 2 hours daily from Day 1 to Day 5 following CWP232291 infusion.~For cohort 4, a fixed dose of ara-C at 1 G/m2 will be administered IV over 2 hours daily from Day 1 to Day 7 following 250 mg/m2 CWP232291 infusion."

Trial Locations (5)

77030

The University of Texas MD Anderson Cancer Center, Houston

98195

University of Washington, Seattle

Unknown

Samsung medical center, Seoul

Seoul National University Hospital, Seoul

Asan Medical Center, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

JW Pharmaceutical

INDUSTRY

NCT03055286 - Clinical Study of CWP232291 in Acute Myeloid Leukemia Patients | Biotech Hunter | Biotech Hunter