The objective of the study is to evaluate tolerability and safety of CBT101 in patients who underwent curative surgery and adjuvant therapy for solid cancer
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
6
CBT101 cells, every 4 weeks
CBT101 cells, every 4 weeks
CHA Bundang Medical Center
Seongnam-si, Gyeonggi-do, South Korea
Dose limiting toxicity (DLT)
Dose limiting toxicity (DLT)
Time frame: 29 days
Disease-free survival rate (DFS)
Disease-free survival rate (DFS)
Time frame: 6 months
Oerall survival rate (OS)
Oerall survival rate (OS)
Time frame: 6 months
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