Targeting the Pathophysiology of Sickle Cell-Related Kidney Disease Using the SGLT2 Inhibitors, Empagliflozin
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Illinois at Chicago
- Study ID
- NCT07175051
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Albuminuria
- Sickle Cell Anemia (HbSS, or HbSβ-thalassemia0)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 60 Years
- Healthy Volunteers
- Not accepted
Interventions
- Empagliflozin (oral) — DRUG10 mg
Study Details
Sickle cell anemia (SCA) is an inherited red blood disorder. The kidneys are among the most commonly affected organ systems in SCA. The Food and Drug Administration (FDA) has approved empagliflozin as a treatment to reduce the decline of kidney function in those with kidney disease. The proposed research study aims to determine whether empagliflozin can prevent the progression of kidney dysfunction in patients with sickle cell anemia (SCA) who are at high risk of developing advanced chronic kidney disease (CKD).
Key Dates
- Start date
- Apr 8, 2026
- Status verified
- May 2026
- Primary completion
- Oct 31, 2029
- Completion
- Oct 31, 2030
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TreatmentEmpagliflozin
Primary Outcome Measure
Efficacy of empagliflozin - urine biomarker: Adenosine [ Time Frame: From enrollment to the end of treatment at 48 weeks ]
Central Contacts
- Santosh L Saraf, MD312-996-5680
- Anand Srivastave, MD
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Illinois Chicago, Sickle Cell Center | Chicago | Illinois | 60302 | Anand Srivastava, MD |
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