Efficacy and Safety Study of SyB L-0501 for Patients With Chronic Lymphocytic Leukemia

PHASE2CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

January 31, 2013

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2015

Conditions
Chronic Lymphocytic Leukemia
Interventions
DRUG

SyB L-0501

SyB L-0501 is administered at 100 mg/m2/day by intravenous infusion on Day 1 and Day 2 followed by 26 days of monitoring. This is considered to be one cycle and may be repeated up to 6 cycles. Dose administration can be delayed or discontinued from the second cycle as necessary according to adverse events and the results of monitoring during the previous cycle, but dose reduction is permitted from the 3rd cycle.

Trial Locations (6)

Unknown

Research Site, Nagoya

Research Site, Fukuyama

Research Site, Kagoshima

Research Site, Isehara

Research Site, Izumo

Research Site, Minato-ku

Sponsors
All Listed Sponsors
lead

SymBio Pharmaceuticals

INDUSTRY