The purpose of the study is to determine if AMG 706 will have clinically meaningful anti-tumor activity in subjects with locally advanced or metastatic thyroid cancer who are not candidates for radioactive iodine therapy or local therapies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
184
Objective Response Rate (complete response and partial response) as defined by modified RECIST
Duration of response
Progression Free Survival
Changes in tumor markers
overall survival time
time to response
Tumour Related Symptoms (medullary thyroid cancer arm)
AMG 706 pharmacokinetic profile
patient reported outcome (EQ-5D)
Safety Endpoint: Incidence of treatment-emergent adverse events (including all, serious, treatment-related, and each by maximum severity).
Pharmacokinetic Enpoint: AMG 706 pharmacokinetic parameters (Cmax, t1/2, AUC0-24,C24)
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