Prospective, Basket, Open-label, Multi-dose, Single-arm, Simon's two-stage, Multi-center trial Study drug : neratinib + herzuma (trastuzumab biosimilar)
1. Primary objective Evaluate overall response rate (ORR) in HER2 mutated advanced solid cancer patients based on RECIST v1.1 2. Secondary objectives (1) Evaluate clinical benefit rate (CBR) (2) Evaluate duration of response (DOR) (3) Evaluate progression free survival (PFS) (4) Evaluate overall survival (OS) (5) Evaluate compliance with oral administration 3) Safety evaluation 1. Evaluate the overall safety of the test drug 2. Evaluate the predefined adverse event (diarrhea)
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
42
* neratinib 240mg po daily * herzuma 8mg/kg (loading) --\> 6mg/kg q3w
Korea university Guro hospital
Seoul, South Korea
overall response rate (ORR)
ORR according to RECIST v1.1
Time frame: at 6 months
clinical benefit rate, CBR
CR+PR + SD more than 12 weeks
Time frame: at 6 months
median duration of response, DOR
DOR is related to the quality of life and is one of the methods for evaluating tumor response approved by pharmaceutical regulatory agencies
Time frame: at 6 months
median progression free survival, PFS
from enrollment to disease progression, death or withdrawal
Time frame: at 6 months
safety profiles
safety profiles according to CTCAE 4.0
Time frame: at 6 months
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