This study is a single arm study to access the anti-tumor efficacy and safety of sunvozertinib in untreated advanced NSCLC patients with EGFR uncommon mutations.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
34
sunvozertinib monotherapy, 300mg QD
sunvozertinib monotherapy, 200mg QD
Fudan university shanghai cancer center
Shanghai, China
RECRUITINGObjective Response Rate(ORR)
Time frame: from first dose to last dose ,up to 24 months
Progression-free survival (PFS)
Time frame: from first dose to first documented disease progression assessed by investigator or death due to any cause up to 48 months ,up to 18 months
Duration of Response (DoR)
Time frame: for subject with PR or CR defined as the time from the first dose documentd CR or PR to disease progression or death up to 18 months
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