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Open label, multi-center, expanded access study for renal transplant patients with once daily Envarsus XR (Tacrolimus).
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.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Tacrolimus | Drug | Open label, multi-center, expanded access study for renal transplant patients with once daily Envarsus XR. |
|
Inclusion Criteria:
Eligible patients will fulfill all of the following criteria:
Exclusion Criteria:
Patients fulfilling any of the following criteria are NOT eligible for study inclusion:
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
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| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| ID | Term |
|---|---|
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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| ID | Term |
|---|---|
| D016559 | Tacrolimus |
| ID | Term |
|---|---|
| D018942 | Macrolides |
| D007783 | Lactones |
| D009930 | Organic Chemicals |
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| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |