purpose Primary endpoint * To evaluate the 24 month disease free survival Second endpoints * To evaluate the 24 month overall survival To analyze the toxicity and the quality of life
Approximately 48 month from the date of IRB approval Patients enrolled in this study targets approximately 314 people. Completion of patient enrollment is expected to take approximately 24 month, approximately 24 month follow-up period is expected to be needed
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
314
Subjects assigned to Arm I Neople taksoljuwa Latin week the first day of the week based outpatient / inpatient treatment receive it. The subjects first received taksoljureul given over 3 hours followed by 30 minutes will be administered Neople Latin week.
Korea Institute of Radiological and Medical Sciences
Seoul, South Korea
24month progression free survival
Time frame: 24 months
Toxicity Profile
Time frame: 24 months
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