A Study of the Safety and Tolerability of BMS-986183 in Patients With Liver Cancer



Status:Active, not recruiting
Conditions:Liver Cancer, Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/17/2018
Start Date:August 23, 2016
End Date:October 22, 2020

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A Phase 1/2 Study of BMS-986183 in Subjects With Advanced Hepatocellular Carcinoma

The purpose of this study is to evaluate the safety and tolerability of BMS-986183 in
patients with liver cancer.


For more information regarding Bristol-Myers Squibb Clinical Trial participation, please
visit www.BMSStudyConnect.com

Inclusion Criteria:

- Must have advanced liver cancer that cannot be treated with surgery or other local
methods

- Liver cancer is confirmed by a microscopic examination of tissue

- Liver disease is classified as 'A' by a standard method called Child-Pugh score

- Daily living abilities are classified as '0 or 1' by a standard method from the
Eastern Cooperative Oncology Group (ECOG)

- Women must use contraception

Exclusion Criteria:

- Prior liver transplant

- Increase in blood pressure in some of the veins entering the liver

- Cancer that has spread to the brain or the layers of tissue that cover the brain or
spinal cord

- Infection with both hepatitis B and C, both hepatitis D and B, infection with HIV, or
other infections

- Disease of the heart or blood vessels around the heart

- Active cancers within the last 2 years

- No more than 2 prior systemic treatments or other investigational agents except
PD-1/PD-L1 or Ipilimumab (Part 2)

- Currently on anti-platelet or anti-coagulation therapy

- Radiotherapy within 4 weeks of treatment

- Any major allergies

Other protocol defined inclusion/exclusion criteria could apply
We found this trial at
3
sites
Los Angeles, California 90095
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Los Angeles, CA
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Ottawa, Ontario
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Ottawa,
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Portland, Oregon 97201
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Portland, OR
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