Study to Evaluate the Safety and Efficacy of Pazopanib, in Subject With Refractory Solid Tumors
Study to Evaluate the Safety and Efficacy of Pazopanib, in Subject With Refractory Solid Tumors
This study is a single arm, pilot study of pazopanib in patient with FGFR2 amplification Refractory solid tumor and/or specific sensitivity to pazopanib by Avatar scan that has progressed following standard therapy or that has not responded to standard therapy or for which there is no standard therapy.
To investigate the efficacy and safety of pazopanib in patient with Refractory solid tumor.
Inclusion Criteria:
Provision of fully informed consent prior to study specific procedures.
Patients must be >= 19 years of age
FGFR2 amplification ,Refractory solid tumor and/or specific sensitivity to by Avatar scan that has progressed following standard therapy or that has not responded to standard therapy or for which there is no standard therapy.
ECOG Performance status0-2
Have measurable or evaluated disease based on RECIST 1.1 as determined by investigator.
Adequate Organ Function Laboratory values
Patients of child-bearing potential should be using adequate contraceptive measures should not be breast feeding and must have a negative pregnancy test prior to start of dosing
Adequate heart function
Exclusion Criteria: