Transplant of Redeemed Organs by Judicious Administration of New Direct-Acting Antivirals for Hepatitis-C Heart Recipients

ConditionHeart Failure
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-90
SponsorBaylor Research Institute

About this trial

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®).

Eligibility criteria

Qualifiers

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)

Disqualifiers

Listed for combined organ transplant

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,

Trial design

Treatments tested in this trial

  • Epclusa

Treatment groups

15 Participants
are divided into 1 treatment group

Sponsors and collaborators