Once-daily Regimen With Envarsus® to Optimize Immunosuppression Management and Outcomes in Kidney Transplant Recipients

A once-daily immunosuppressant regimen comprising of Envarsus-everolimus-prednisone will have
6-month treatment failure rates that are non-inferior to the twice-daily regimen of
Envarsus-mycophenolate mofetil-prednisone and will have improved patient-reported adherence.

1. Inclusion criteria

1. Male or female adult (≥18 years old) with a history of solitary kidney transplant
within 3 months (±2 months) of transplant with self-reported medication adherence
issues, as indicated by a MMAS-8 of at least 1.

2. Patients must be capable of understanding the purposes and risks of the study and have
the ability to give written informed consent and be willing to participate and comply
with the study.

3. Women of childbearing potential must have a negative pregnancy test within the 48
hours prior to receiving study medication.

4. Women of childbearing potential and sexually active males must be willing to use
contraception, as indicated in Section 6 of the protocol. Subjects who are not of
reproductive potential (status post bilateral tubal ligation, bilateral oophorectomy,
hysterectomy, or vasectomy), not sexually active, whose current partner(s) is not of
reproductive potential, or whose sexual activity is exclusively homosexual are
eligible without requiring the use of contraception.

2. Exclusion criteria

1. Patients will be excluded if they are pregnant or nursing females or males with a
pregnant female partner

2. Recipient of multiple organ transplant

3. Recipient of a non-renal organ

4. Proteinuria > 800 mg/24 hour

5. eGFR < 30 ml/min

6. WBC ≤ 2k/mm3

7. Plt ≤ 50k/mm3

8. Triglycerides > 500 mg/dL

9. HIV positive (HIV ab +)

10. Unable to tolerate oral medications

11. Use of another investigational product within thirty days prior to receiving study
medication

12. Acute graft rejection within the past month (Banff 1A or higher) or received an ABO
incompatible donor organ.

13. A condition or disorder that, in the opinion of the investigator, may adversely affect
the outcome of the study or the safety of the subject