A Study of Safety Tolerability and Clinical Activity of MEDI4736 and Tremelimumab Administered as Monotherapy and in Combination to Subjects with Unresectable Hepatocellular Carcinoma
Investigation of Safety of Investigational Medications in Liver Cancer Treatment
Brief description of study.
The purpose of this study is to see if two investigational drugs, called MEDI4736 and tremelimumab (either drug alone or in combination) are safe in treating adult subjects with liver cancer (hepatocellular carcinoma) that cannot be removed by surgery (unresectable).
Detailed description of study
The purpose of this study is to see if two investigational drugs, called MEDI4736 and tremelimumab are safe in treating adult subjects with liver cancer that cannot be removed by surgery.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: liver cancer,hepatocellular carcinoma
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Age: 18 years - 100 years
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Gender: All
Inclusion Criteria
In order to be eligible to take part in this trial, patients must meet the following criteria:
- 18 years or older
- Confirmed diagnosis of unresectable hepatocellular carcinoma with or without concomitant viral hepatits B or hepatitis C infection
For a full list of participation criteria, please visit clinicaltrials.gov.
This study investigates the safety of two investigational medications in treating adults with liver cancer that cannot be removed by surgery. The medications are being tested alone and in combination to evaluate their effects on liver cancer, also known as hepatocellular carcinoma.
Participants in this study will undergo treatment with either one of the investigational medications or a combination of both. The study will monitor the safety and effects of these treatments on the participants.
- Who can participate: Adults aged 18 years or older with liver cancer that cannot be removed by surgery are eligible. Participants may have a diagnosis with or without viral hepatitis B or C infection.
- Study details: Participants will receive treatment with investigational medications. The study will monitor the safety of these medications. If applicable, a placebo will be used to compare against the investigational treatments.