The purpose of this study is to determine whether brivanib is an effective treatment for liver cancer in Asian patients who have failed or could not tolerate sorafenib therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
87
Compare overall survival of subjects with advanced HCC who have progressed on/after or are intolerant to sorafenib and receive brivanib plus best supportive care (BSC) to those receiving placebo plus BSC
Time frame: Every 6 weeks for an average of 6 months
Compare time to progression (TTP) using modified RECIST for HCC
Time frame: Every 6 weeks
Compare objective response rate (ORR) and disease control rate (DCR) using modified RECIST for HCC
Time frame: Every 6 weeks
Assess duration of response, duration of disease control and time to response
Time frame: Every 6 weeks
Assess serious and nonserious adverse events, laboratory evaluations, significant physical examination findings and ECG results
Time frame: Every 6 weeks
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Local Institution
Hefei, Anhui, China
Local Institution
Beijing, Beijing Municipality, China
Local Institution
Beijing, Beijing Municipality, China
Local Institution
Beijing, Beijing Municipality, China
Local Institution
Chongqing, Chongqing Municipality, China
Local Institution
Fuzhou, Fujian, China
Local Institution
Fuzhou, Fujian, China
Local Institution
Guangzhou, Guangdong, China
Local Institution
Guangzhou, Guangdong, China
Local Institution
Guanzhou, Guangdong, China
...and 22 more locations