This clinical trial aims to evaluate the efficacy, safety of Anlotinib in advanced solid tumors with FGFR alteration.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Anlotinib
Shanghai Changzheng Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGShanghai Changzheng Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGShanghai Changzheng Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGObjective Response Rate(ORR)
Evaluation of tumor burden based on RECIST criteria.
Time frame: up to 36 months
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