An Exploratory Investigation of the Safety of Empagliflozin in Kidney Transplant Recipients (SEKTR)

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Kidney transplantation improves the health and quality of life for those Veterans with end stage kidney disease (ESKD). While early patient and graft survival are excellent, long-term outcomes continue to be challenging. Patient death with existing kidney graft function occurs in about half of all recipients over time. This is primarily due to the development of cardiovascular disease in a patient population with multiple preexisting cardiac disease risk factors. There has been little progress in improving outcomes in this area for over two decades. Recent studies in chronic kidney disease (CKD) patients using SGLT2 inhibitors (SGLT2i), regardless of the presence of type 2 diabetes mellitus (T2DM), results in both kidney protective and cardiac protective impacts and improved patient outcomes. However, kidney transplant recipients (KTRs) were excluded from these clinical trials due to concerns that these agents promote infection, diminish graft function, and may alter immunosuppressive drug levels that are the mainstay of patient's transplant therapy. There are limited published data of SGLT2i treatment of selected KTRs.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Adult (\>18 years of age) male and female recipients (all races and ethnicities)

• Subject must be able to understand and provide consent

• Recipient of a primary or secondary kidney transplant at least 3 months or longer since transplant

• For subjects with T2DM or post-transplant diabetes (PTDM), measured kidney function by CKD epi eGFR must be 30mL/min/1.73m2 to \< 45ml/min/1.73m2 or CKD epi eGFR 45 mL/min/1.73m2 to 90ml/min/1.73m2 with urinary albumin:creatinine ratio 200 mg/g (or protein:creatinine 300 mg/g).

• For subjects without T2DM or PTDM: measured kidney function by CKD epi eGFR must be 20mL/min/1.73m2 to \< 45ml/min/1.73m2 or CKD epi eGFR 45 mL/min/1.73m2 to 90ml/min/1.73m2 with urinary albumin:creatinine ratio 200 mg/g (or protein:creatinine 300 mg/g).

Locations
United States
Iowa
Iowa City VA Health Care System, Iowa City, IA
RECRUITING
Iowa City
Illinois
Edward Hines Jr. VA Hospital, Hines, IL
NOT_YET_RECRUITING
Hines
Nebraska
Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NE
RECRUITING
Omaha
Pennsylvania
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
RECRUITING
Pittsburgh
Tennessee
Tennessee Valley Healthcare System Nashville Campus, Nashville, TN
RECRUITING
Nashville
Contact Information
Primary
Roslyn B Mannon, MD
roslyn.mannon@va.gov
(205) 999-7362
Backup
Ramesh K Ramalingam
Ramesh.Ramalingam@va.gov
(402) 995-4873
Time Frame
Start Date: 2024-04-05
Estimated Completion Date: 2030-03-31
Participants
Target number of participants: 264
Treatments
Other: Empagliflozin
Open Label, Empagliflozin 12.5 mg QD
Sponsors
Leads: VA Office of Research and Development
Collaborators: VA Tennessee Valley Health Care System, Iowa City VA Health Care System, VA Hines Health Care, VA Pittsburgh Healthcare System

This content was sourced from clinicaltrials.gov