This is a prospective, open, phase I clinical study to evaluate the safety and tolerability of a CDK4 / 6 inhibitor and a MEK inhibitor in the treatment of metastatic digestive system tumors
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Participant will receive a CDK4 / 6 inhibitor and a MEK inhibitor treatment to determine the maximum tolerated dose
Henan Cancer Hospital
Zhengzhou, Henan, China
RECRUITINGTo determine the maximum tolerated dose of a CDK4 / 6 inhibitor and a MEK inhibitor therapy
Time frame: Up to approximately 24 months
ORR
the Objective Remission Rate
Time frame: Up to approximately 24 months
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