Evaluate the efficacy,safety and pharmacokinetics of HLX208 in advanced non-small cell lung cancer patients with BRAF V600 mutation
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
450mg bid, take orally
Shanghai chest hospital
Shanghai, China
RECRUITINGORR
The number of patients with CR or PR divided by the total number of treated
Time frame: from first dose to the last patient was followed up for 6 month
PFS
Progression-free survival
Time frame: the time (month is regarded as the unit) from the first dose to the date of first documented progression or date of death from any cause, whichever came first,through treatment completion, an average of about 1 year
DOR
Duration of response
Time frame: from the first occurrence of a documented CR or PR (whichever recorded earlier) to the time of first documented disease progression or death (whichever occurs first),through treatment completion, an average of about 1 year
OS
Overall survival
Time frame: from the first dose to the time of death due to any cause, an average of about 2 year
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