HCV-RNA Kinetics During Sorafenib for Hepatocellular Carcinoma (HCC)
Stopped early · Phase 4
Conditions studied: Hepatocellular Cancer
In brief
This research study is a Phase IV clinical trial. Phase IV trials are used to further test and monitor the safety of a drug approved by the FDA and to see if the drug has any other indications that can be used to treat different diseases. Sorafenib is a new drug, which is approved under the brand name Nexavar for the treatment of liver cancer. It is also currently being tested in various other cancers. Sorafenib works by slowing down and/or stopping the development of new cancer cells and new blood vessels. By slowing down and/or stopping the growth of new blood vessels around a tumor, it is believed that sorafenib prevents or slows down the growth of tumors. The researchers of this study would like to study the effects of sorafenib on hepatitis C by drawing additional research blood samples from people infected with hepatitis C who are receiving sorafenib treatment for liver cancer. These tests will measure certain proteins in the blood (HCV-RNA) which may indicate if sorafenib has any effect on the hepatitis C virus.
Key facts
- Study ID
- NCT01849588
- Run by
- Massachusetts General Hospital
- People needed
- 3
- Starts
- 2013-05-01
- Expected to finish
- 2017-01-01
- Last updated by the study team
- 2017-04-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologically and/or radiologically confirmed advanced HCC
- Detectable HCV RNA with anti-HCV-positivity
- Life expectancy of at least 3 months
- Willing to use adequate contraception
You may not qualify if…
- Pregnant or breastfeeding
- Undetectable HCV RNA
- Uncontrolled hypertension
- Active or clinically significant cardiac disease
- Thrombolic, embolic, venous or arterial events within 6 months of informed consent
- Pulmonary hemorrhage/bleeding event (NCI-CTCAE grade 2 or higher) within 4 weeks before study entry
- Previously untreated or concurrent cancer except cervical cancer in situ, treated basal cell carcinoma or superficial bladder tumor
- Presence of non-healing wound, ulcer or bone fracture
- History of organ allograft
- Known or suspected allergy or hypersensitivity to any of the study drugs
- Any malabsorption condition
- Inability to comply with the protocol and/or not willing or not available for follow up
- Major surgery within 30 days prior to start of study drug
Where it is running
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Brigham and Women's Hospital — Boston, Massachusetts, United States
- Dana-Farber Cancer Institute — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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