This is a phase 1b, dose escalation and expansion study to evaluate the safety, tolerability, pharmacokinetics and efficacy of JMKX001899 in combination with IN10018 or in combination with chemotherapy or in combination with IN10018 and chemotherapy in subjects with locally advanced or metastatic NSCLC with KRAS G12C mutation.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
72
JMKX001899 tablet administered orally daily.
IN10018 tablet administered orally daily.
IV infusion once every 3 weeks
Guangdong Provincial People's Hospital
Guangzhou, Guangdong, China
RECRUITINGRecommended Phase II dose (RP2D)
Time frame: approximately 1 year
adverse events
Time frame: Through study completion, approximately 2.5 years
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IV infusion once every 3 weeks, 4 Cycles