Assessment of Safety and Efficacy of SGLT2is Among LN Patients

Sponsor
Ain Shams University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06113900
Collaborator
(none)
50
1
2
14
3.6

Study Details

Study Description

Brief Summary

The aim of this study is to assess the safety and efficacy of SGLT2is among LN patients.

Condition or Disease Intervention/Treatment Phase
  • Drug: Dapagliflozin 10mg Tab orally once daily
Phase 1/Phase 2

Detailed Description

SLE is a chronic debilitating autoimmune disorder that involves multiple organ systems either simultaneously or sequentially with relapsing and remitting course. The word 'Lupus' is a Latin term which means wolf.

Lupus nephritis (LN) is one of the common complications in patients with SLE and influences overall outcome of these patients. About two-thirds of patients with SLE have renal disease at some stage which is a leading cause of mortality in these patients.

Manifestations of LN vary from asymptomatic urinary abnormalities to rapidly progressive crescentic glomerulonephritis to end-stage renal disease (ESRD).

Recently, metabolic modulation approach has become a hot spot in the management of SLE. Increased glucose metabolism in immune cells has been reported in patients with SLE.

Repurposing metformin, an old anti diabetic drug, has the potential to reduce the risk of lupus flare in randomized controlled trials. A recent crossover study implied that peroxisome proliferator-activated receptor-gamma agonists might decrease cardiovascular risk in patients with SLE.

Dapagliflozin, SGLT2i, is a new therapy for type 2 diabetes. The Dapagliflozin mode of action is to reduce glucose reabsorption in the epithelial cells of the proximal renal tubule of the kidney, which results in decreased blood glucose and glycated hemoglobin levels.

Strikingly, four cardiovascular outcome trials demonstrated that treatment with SGLT2is (empagliflozin, canagliflozin and dapagliflozin) in patients with type 2 diabetes had prominent effects on slowing the decline rate of eGFR and decreasing albuminuria, as well as a significant reduction in cardiovascular events.

Furthermore, the nephroprotective efficacy of SGLT2is was extended to non-diabetic CKD, such as IgA nephropathy.

The net gain of SGLT2 inhibition is to reduce renal workload and to modulate weight loss and blood pressure.

The paradigm for CKD and congestive heart failure management has been shifted accordingly

Interestingly, all researchers have reported that SGLT2is could block lipopolysaccharide-induced and NLRP3-mediated inflammatory responses and regulate macrophage polarization via interplay with mammalian target of rapamycin (mTOR) and AMP-activated protein kinase pathway thereby, SGLT2is might further contribute to reducing inflammation, modulating endothelial dysfunction and decelerating atherosclerosis which are all relevant to the pathophysiology of SLE.

Here, the investigators initiated this study aiming to assess the safety and efficacy of dapagliflozin among patients with LN.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Assessment of Safety and Efficacy of Sodium Glucose Co-transporter 2 Inhibitors Among Lupus Nephritis Patients
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Jan 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Drug as Dapagliflozin 10 mg orally for 6 months is given

25 lupus nephritis patients will receive SGLT2is as dapagliflozin 10mg beside there usual treatment of lupus for 6 months

Drug: Dapagliflozin 10mg Tab orally once daily
Sodium glucose co-transporter 2 inhibitors
Other Names:
  • Empagliflozin 10 mg tab orally once daily
  • No Intervention: On there conventional lupus nephritis treatment

    25 lupus nephritis patients didn't receive SGLT2i and continue on their conventional lupus nephritis treatment

    Outcome Measures

    Primary Outcome Measures

    1. Renal Function Tests: [6 months]

      Measurement of serum urea level in mg/dl at 3 month's interval, that is, at 0, 3 and 6 months. Measurement of serum creatinine level in mg/dl at 3 month's interval, that is, at 0, 3 and 6 months. Measurement of serum uric acid level in mg/dl at 3 month's interval, that is, at 0, 3 and 6 months.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patients aged more than 18 year.

    • Patients with confirmed SLE according to EULAR/ACR classification criteria.

    • Patients with LN ( persistent proteinuria > 2 gm per day or greater than 3+ by dipstick, and/or cellular casts including red cell, hemoglobin, granular, tubular or mixed & "active urinary sediment" (>5 RBC/hpf, >5 WBC/hpf in the absence of infection, or cellular casts limited to RBC or WBC casts )

    • Patient with e GFR > 25 ml/min/1.73m2 by CKD-EPI equation.

    Exclusion Criteria:
    • Patients with an allergy or intolerance to Dapagliflozin or any prior SGLT2i exposure within 1 month before screening.

    • Medical history of chronic disease (Severe respiratory distress, gastrointestinal tract lesions & chronic liver disease)

    • Patients with recurrent genitourinary infections.

    • Patient with proteinuria < 2gm.

    • Patient who show response to immune therapy in proteinuria reduction > 50%.

    • Patient with Lupus in induction phase.

    • Patient on steroids > 30 mg daily dose.

    • Patients with diabetes mellitus.

    • Patients with severe infection requiring antibiotics within 1 month before screening.

    • Patients with malignant diseases.

    • Pregnant or breast-feeding women.

    • Patients with eGFR < 25 ml/min/1.73m2 or undergoing dialysis therapy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ain Shams University Alexandria Egypt

    Sponsors and Collaborators

    • Ain Shams University

    Investigators

    • Principal Investigator: Howaida Al-Shennawi, Professor, Professor of internal medicine and Nephrology
    • Study Director: Cherry Kamel, Professor, Professor of internal medicine and Nephrology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Marwa Ahmed Mohamed Ahmed Waly, Head of Nephrology Department, Ain Shams University
    ClinicalTrials.gov Identifier:
    NCT06113900
    Other Study ID Numbers:
    • SGLT2I among LN patients
    First Posted:
    Nov 2, 2023
    Last Update Posted:
    Nov 2, 2023
    Last Verified:
    Oct 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 2, 2023