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Search / Trial NCT01108705

Comparison of Brivanib and Best Supportive Care (BSC) With Placebo and BSC for Treatment of Liver Cancer in Asian Patients Who Have Failed Sorafenib Treatment

Launched by BRISTOL-MYERS SQUIBB · Apr 21, 2010

Trial Information

Current as of July 21, 2025

Terminated

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Key Inclusion Criteria:
  • Diagnosis of advanced hepatocellular carcinoma
  • Asian ethnicity
  • Patient has failed ≥14 days of sorafenib treatment
  • Cirrhotic status of Child-Pugh Class A or B with a score of 7
  • Eastern Cooperative Oncology Group performance status of 0, 1, or 2
  • Life expectancy of at least 8 weeks
  • Adequate hematologic, hepatic, and renal function
  • Key Exclusion Criteria:
  • Women of childbearing potential who are unwilling or unable to use an acceptable method to avoid pregnancy
  • Previous or concurrent cancer that is distinct in primary site
  • History of active cardiac disease
  • Thrombotic or embolic events within the past 6 months
  • Inability to swallow tablets or untreated malabsorption syndrome
  • History of HIV infection
  • Prior use of systemic investigational agents for hepatocellular carcinoma (except sorafenib)

About Bristol Myers Squibb

Bristol-Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a robust portfolio of products across multiple therapeutic areas, including oncology, immunology, cardiovascular, and fibrotic diseases, BMS emphasizes cutting-edge research and a commitment to advancing medical science through clinical trials. The company is driven by a mission to provide transformative therapies, leveraging collaboration and scientific expertise to address unmet medical needs and improve patient outcomes worldwide.

Locations

Singapore, , Singapore

Taoyuan, , Taiwan

Taipei, , Taiwan

Seoul, , Korea, Republic Of

Kaohsiung County, , Taiwan

Gyeonggi Do, , Korea, Republic Of

Hefei, Anhui, China

Chongqing, Chongqing, China

Guangzhou, Guangdong, China

Nanjing, Jiangsu, China

Suzhou, Jiangsu, China

Changchun, Jilin, China

Chengdu, Sichuan, China

Shenyang, Liaoning, China

Shanghai, Shanghai, China

Guanzhou, Guangdong, China

Wuhan, Hubei, China

Beijing, Beijing, China

Hangzhou, Zhejiang, China

Fu Zhou, Fujian, China

Fuzhou, Fujian, China

Ha Erbin, Heilongjiang, China

Hankou, Hubei, China

Chang Chun, Jilin, China

Tianjing, Tianjin, China

Xi An, , China

Xi'an, , China

Patients applied

0 patients applied

Trial Officials

Bristol-Myers Squibb

Study Director

Bristol-Myers Squibb

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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