Expanded Access Study for Renal Transplant Patients With Envarsus XR ™
- Conditions
- Renal Failure
- Registration Number
- NCT02411604
- Lead Sponsor
- Veloxis Pharmaceuticals
- Brief Summary
Open label, multi-center, expanded access study for renal transplant patients with once daily Envarsus XR (Tacrolimus).
- Detailed Description
The study is designed to facilitate expanded access of Envarsus XR treatment to renal transplant patients. Patients are identified by the site investigator as a patient who has experienced favorable outcomes while in an Envarsus XR (LCP-Tacro) clinical study and/or the site investigator has identified a renal transplant patient with a medical need for an alternative tacrolimus treatment versus the patient's current tacrolimus treatment.
Recruitment & Eligibility
- Status
- APPROVED_FOR_MARKETING
- Sex
- All
- Target Recruitment
- Not specified
-
Eligible patients will fulfill all of the following criteria:
- Patient age ≥18years old
- Willing to give written informed consent and is able to speak, write and understand English
- Patient understands potential risks or benefits with treatment of Envarsus XR
- Patients who have received a primary or secondary kidney transplant
- Patient who have received prior treatment with Envarsus XR (LCP-Tacro) and who are not currently participating in an Envarsus/LCP-Tacro study OR
- The treating Investigator has identified the patient as having a medical necessity for switching from their current tacrolimus treatment to Envarsus XR: Investigator is aware the medical necessity for switching is not related to the inability to purchase available tacrolimus.
-
Patients fulfilling any of the following criteria are NOT eligible for study inclusion:
- Recipients of organ transplants other than kidney
- Pregnant or nursing (lactating) women, or planning to become pregnant, where pregnancy is defined as a state of female after conception and until the termination of gestation, confirmed by a positive hCG serum or urine laboratory test.
- Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant who are unwilling to use a defined SOC method of contraception, UNLESS they are
-
Women whose career, lifestyle, or sexual orientation preclude intercourse with a male partner
-
Women whose partners have been sterilized by vasectomy or other medically approved means
Study & Design
- Study Type
- EXPANDED_ACCESS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method