The primary purpose of this study is to evaluate the efficacy and safety of WX-0593 in patients with ALK-positive NSCLC
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
WX-0593 Tablets 60 mg QD,once daily for 7 days, followed by 180 mg of WX-0593 tablets,once daily in a 21-days cycle.
Shanghai Jiao Tong University Chest Hospital
Shanghai, China
Objective Response Rate (ORR) Assessed By independent radiology review
ORR is defined the percentage of the participants who have achieved complete response (CR) or partial response (PR) per independent radiology review using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 after the initiation of study treatment.
Time frame: From first administration to the date that the last patients observed for 18 weeks
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