Transplant of Redeemed Organs by Judicious Administration of New Direct-Acting Antivirals for Hepatitis-C Heart Recipients
Recruiting · NCT03383419 · Interventional (participants receive a specific treatment) · Lead sponsor: Baylor Research Institute
View the official record on ClinicalTrials.gov →Interventions studied
Epclusa
What this trial is about
This phase II, multi-center, open-label study will evaluate the safety and efficacy of utilizing HCV-positive donors for heart transplant in HCV-negative recipients treated with sofosbuvir 400 mg / velpatasvir 100 mg (Epclusa®).
Who can take part
Age range
18 Years to 90 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 2
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Willing and capable of providing written informed consent
- Age ≥ 18 years
- Listed for isolated orthotopic heart transplant
- HCV seronegative (or, if HCV seropositive, then subject must be PCR negative on at least 2 draws consistent with a spontaneously cleared or fully-treated and cleared prior infection; in this case last anti-HCV antiviral dose must be ≥12 weeks ago and 2 negative titers ≥12 weeks after completion of the antiviral regimen)
Exclusion criteria
- Listed for combined organ transplant
- Any of the following liver disease states, including:
- History of HCV viremia detectable by either HCV qualitative or quantitative PCR unless deemed cured (SVR-12),
- Hepatitis B surface Ag positive(unless clinically determined to be previously negative and acutely positive due to vaccination with recombinant surface antigen) or detectable hepatitis B DNA,
- Cirrhosis, as indicated by liver biopsy,
- Portal hypertension as indicated by a hepatic venous pressure gradient \> 5 mm Hg and/or the presence of esophageal varices e.) ALT and AST \> 3x ULN unless adjudicated to be from a non-hepatic cardiac or skeletal muscle source,
- History of prior solid organ transplant
- Pregnant individuals
- History of HIV infection
- History of severe renal disease currently requiring dialysis. Chronic kidney disease with creatinine clearance \<30 ml/min/1.73m2 (by MDRD method) at screening or on last two consecutive measurements before acceptance of transplant organ offer
- Patients who have undergone or who will undergo immune desensitization therapy
- Prospective-positive cross-match or predicted positive cross-match
- Patients unwilling to notify their sexual partner(s) of participation in this trial
Where it is running
3 locations listed across 3 US states.
- Cedars-Sinai Medical Center - Los Angeles, California, United States
- Duke University Medical Center - Durham, North Carolina, United States
- Baylor University Medical Center - Dallas, Texas, United States