Ignite Creation Date:
2024-05-06 @ 9:18 AM
Last Modification Date:
2024-10-26 @ 12:13 PM
Study NCT ID:
NCT02956005
Status:
TERMINATED
Last Update Posted:
2020-03-24
First Post:
2016-11-02
Brief Title:
Envarsus XR in African American Renal Transplant Recipients
Sponsor:
Georgetown University
Organization:
Georgetown University
Study Overview
Official Title:
Envarsus XR in African American Renal Transplant Recipients
Status:
TERMINATED
Status Verified Date:
2016-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
IIS - PI left the institution Subjects just followed to study completion
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
EXR
Brief Summary:
The purpose of this study is to collect data prospectively on African American patients who are taking the immunosuppressant Envarsus post kidney transplant We are looking to see if African American renal transplant recipients that receive Envarsus will have less tubular injury and calcenurin inhibitor toxicity compared with patients that receive tacrolimus IR
African americans have the higher rates of CYP3A5 which is associated with the need of higher tacrolimus dose to achieve an adequate level and this many times is associated with signs and symptoms of tacrolimus toxicity such as tremors headaches and neuropathies
The retrospective cohort will be African American patients that will be matched by age gender type of kidney transplant living vs deceased and level of sensitization
African americans have the higher rates of CYP3A5 which is associated with the need of higher tacrolimus dose to achieve an adequate level and this many times is associated with signs and symptoms of tacrolimus toxicity such as tremors headaches and neuropathies
The retrospective cohort will be African American patients that will be matched by age gender type of kidney transplant living vs deceased and level of sensitization
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None