This is a phase 1/2, open label study of D-1553 in combination with IN10018 to assess the safety and tolerability, identify the MTD and RP2D, evaluate the PK properties and antitumor activities in subjects with advanced or metastatic solid tumor with KRasG12C mutation
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
92
Zhejiang Cancer Hospital, Cancer Hospital of the University of Chinese Academy of Sciences,
Hangzhou, Zhejiang, China
adverse events
Number of subjects participants with adverse events
Time frame: Through study completion, approximately 3 years
Objective response rate (ORR) per RECIST v1.1
Defined as the proportion of patients with complete response (CR) or partial response (PR).
Time frame: Through study completion, approximately 3 years
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