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NCT03383419RecruitingPhase 2

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

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

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®).

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
15 (estimated)
First submitted
7 Dec 2017
Start date
20 Mar 2018
Primary completion date
30 Dec 2026
Lead sponsor
Baylor Research Institute
NCT number
NCT03383419

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 15
  • From 20 Mar 2018 to the primary completion date, 30 Dec 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Listed for combined organ transplant
  • History of prior solid organ transplant
  • Patients who have undergone or who will undergo immune desensitization therapy

Other illness

  • History of HIV infection

Lab values

  • 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 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

Other

  • Pregnant individuals
  • Prospective-positive cross-match or predicted positive cross-match
  • Patients unwilling to notify their sexual partner(s) of participation in this trial

Who the study is looking for

  • 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)

Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Baylor University Medical Center
Coordinator of this site? Confirm its status
DallasUnited StatesRecruiting
Duke University Medical Center
Coordinator of this site? Confirm its status
DurhamUnited StatesActive, not recruiting
Cedars-Sinai Medical Center
Coordinator of this site? Confirm its status
Los AngelesUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.