Compliance, Patient, Graft Failure, Heart Transplant Rejection
Conditions
Keywords
Heart Transplant
Brief summary
This phase II, single-center, open-label study will evaluate the comparable efficacy of tacrolimus extended release tablets (Envarsus®) to the standard of care (SOC) twice daily tacrolimus (Prograf®) dosing regimen post-cardiac transplantation.
Detailed description
This is a prospective, open-label, 2-arm, clinical trial to evaluate the efficacy of extended release tacrolimus (Envarsus) once-daily in comparison to Prograf capsules twice-daily after heart transplantation receiving the standard of care twice daily dosing with tacrolimus (Prograf). Secondary objectives are to compare the compliance, safety and efficacy of once a day dosing (Envarsus) versus twice a day dosing (Prograf) and to evaluate the short term safety and tolerability of Envarsus. Approximately 25 adult male or female recipients of a heart transplant will be prospectively enrolled to once-daily therapy with Envarsus tablets. Time of initiation will follow current standard of care. In addition, 25 age/gender-matched subjects who are receiving twice daily dosing with Prograf will be identified from the transplant center database and contacted to be consented, after which their results will be analyzed retrospectively. The Termination Visit will occur on Day 182 (± 2 days) for subjects who complete the study treatment. Subjects who receive the first dose of study drug but withdraw from the study or terminate study treatment for any reason should complete all the procedures outlined for the Termination Visit. The follow-up safety assessment may be conducted via telephone or at a study visit if needed for clinical follow-up on any safety issues). The follow-up safety assessment is to take place approximately 30 days (±5 days) after the last administration of study treatment, whether the subject completed study treatment or withdrew or terminated treatment early.
Interventions
DRUGEnvarsus
Patients will take once daily Envarsus
Sponsors
Baylor Research Institute
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Male or female, ≥ 18 years of age * Able to comply with medication regimen * Subjects must have the capacity to understand and sign the informed consent form * Heart-only transplant recipients
Exclusion criteria
* Subject currently enrolled in another interventional research trial * History of hypersensitivity/adverse reaction to tacrolimus * Patient taking Rapamycin (sirolimus) or cyclosporine (Neoral/Gengraf) * Simultaneous multiple organ transplant recipients * Liver transplant recipients / candidates
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rejection and Graft Failure | 2 years | Evaluate effect on rejection and graft failure by comparing adverse events in standard of care versus experimental groups |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Effect of Compliance on Rejection and Graft Failure | 2 years | To compare complications that lead to acute rejection and graft failure based on patient compliance to once a day dosing versus twice a day dosing |
Countries
United States
Outcome results
None listed