A Multicenter Treatment Protocol of Daclatasvir (BMS-790052) in Combination with Sofosbuvir for the Treatment of Post-Liver Transplant Subjects with Chronic Hepatitis C
Investigational Treatment for Chronic Hepatitis C After Liver Transplant
Brief description of study.
The purpose of this study is to provide an investigational treatment regimen of Daclatasvir plus Sofosbuvir used in combination for 24 weeks in post-liver transplant subjects who have recurrent chronic Hepatitis C Virus (HCV) infection who have a serious or life-threatening condition.
Detailed description of study
The purpose of this study is to provide daclatasvir (DCV) for 24 weeks to be given in combination with sofosbuvir(SOF) to post-liver transplant subjects with chronic hepatitis C recurrence and who have a serious or immediately life-threatening condition, or experienced an event that has decreased their life expectancy to
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: hepatitis
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Age: 18 years - 100 years
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Gender: All
This study investigates an investigational treatment for people who have had a liver transplant and now have chronic Hepatitis C Virus (HCV) infection. Hepatitis C is a liver disease caused by the Hepatitis C Virus. It can lead to serious liver problems, especially in people who have had a liver transplant.
Participants in this study will receive an investigational treatment that combines two medicines for 24 weeks. This treatment aims to manage the recurrence of Hepatitis C after a liver transplant.
- Who can participate: Adults aged 18 and older who have undergone a liver transplant and have a chronic Hepatitis C infection may be eligible. Additional eligibility criteria may apply.
- Study details: Participants will engage in study visits and follow-ups to monitor the effectiveness of the treatment in managing Hepatitis C recurrence after a liver transplant.
- Study Timelines: The study will last 24 weeks.
Interested in the study?
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