LIVE-C-Free: Early and Late Treatment of Hepatitis C With Sofosbuvir/Ledipasvir in Liver Transplant Recipients

Completed · Phase 4

Conditions studied: Hepatitis C

In brief

The predominant remaining questions for post-transplant treatment of Hepatitis C virus (HCV) in the DAA (direct acting anti-virals) era are whether a ribavirin-free regimen is possible and whether pre-emptive treatment is now a potential option to prevent long-term damage to the allograft. Our aim is to provide answers to these primary questions with our multicenter, prospective, randomized, open-label intent-to-treat phase IV study

Key facts

Study ID

NCT02631772

Run by

Medical University of South Carolina

People needed

32

Starts

2016-06-01

Expected to finish

2018-06-30

Last updated by the study team

2019-05-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• At least 18 years of age and able to give informed consent
• History of HCV genotype 1 or 4
• Normal EKG
• At least 91 days post orthotopic liver transplant
• Screening laboratory values within defined thresholds
• Detectable HCV RNA at screening
• Creatinine Clearance of at least 40ml/min using the Cockcroft Gault equation
• Negative pregnancy test for female subjects within 48 hours prior to receiving study medication
• Use of two effective contraception methods if female of childbearing potential or sexually active male unless status post bilateral tubal ligation, bilateral oophorectomy, hysterectomy, or vasectomy

You may not qualify if…

• Serious or active medical or psychiatric illness
• History of significant or unstable cardiac disease
• Stomach disorder that could interfere with the absorption of the study drug
• Pregnant or nursing females or males with a pregnant female partner
• Co-infected with Hepatits B (HBV) or HIV
• Recipients of an allograft from a donor that was infected with HCV with an unknown genotype or non-genotype 1 or 4 unless the recipient is demonstrated to have only genotype 1 or 4 HCV replication post-transplant
• Allergic to or intolerant of sofosbuvir, ledipasvir, or ribavirin
• History of exposure to an Nonstructural protein (NS5A) inhibitor
• Within 1 year of transplant AND history of Hepatocellular Carcinoma (HCC) with tumor burden outside of the Milan Criteria (See Appendix II) prior to transplant
• Participated in a clinical study with an investigational drug or biologic within the last 30 days
• Combined liver/kidney transplant
• History of organ transplant other than liver
• Childs Turcotte Pugh (CTP) B or C
• Patients with fibrosing cholestatic hepatitis
• Platelet count of ≤ 30 k/mm3
• Hemoglobin < 10g/dL
• Total bilirubin > 10mg/dL
• Alanine aminotransferase (ALT),aspartate aminotransferase (AST), or alkaline phosphatase ≥ 10x upper limit normal
• Serum sodium < 125mmol/L
• Current use of any of the Prohibited Interventions (Section 5.3.2) and un-willing to discontinue use, or use of amiodarone within 6 months of screening

Where it is running

• Medstar Georgetown University Hospital — Washington D.C., District of Columbia, United States
• University Hospitals Cleveland Medical Center — Cleveland, Ohio, United States
• University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
• Medical University of South Carolina — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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