JARDIANCE® (Empagliflozin)

The content on this website is in relation to adult patients

 

Mechanism of Action

SGLT2 inhibitors have multiple effects on metabolism and fluid balance in the Cardio-Renal-Metabolic (CRM) interconnected system1

Sodium-glucose cotransporter 2 (SGLT2) is highly expressed in the kidney.1 By blocking reuptake of glucose and sodium in the kidneys SGLT2 inhibitors increase the excretion of both in the urine.1

JARDIANCE® (empagliflozin) mechanism of action diagram

Glycosuria

... which lowers plasma glucose, therefore reduces HbA1C1 and glucose toxicity2

... which causes a caloric loss, resulting in weight loss1,3 and reduction in fat mass1,4

Osmotic diuresis

… which reduces plasma volume, leading to reduction in blood pressure and cardiac preload1,5

Natriuresis

... which alters tubular-glomerular feedback and reduces glomerular hyperfiltration6

... which reduces arterial pressure,7 which improves cardiac afterload5

JARDIANCE® (empagliflozin) is a reversible, highly potent and selective competitive inhibitor of sodium-glucose cotransporter 2 (SGLT2).1

In addition to glucose lowering, JARDIANCE® (empagliflozin) demonstrated secondary benefits of reduction in weight and blood pressure although it is not licensed for this.

The effect of Jardiance (empagliflozin) on the CRM system are mediated via multiple mechanisms

JARDIANCE® (empagliflozin) mechanism of action diagram - CRM system

SGLT2 inhibitors: mode of action18

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JARDIANCE® (empagliflozin) safety profile

Safety Profile

Adverse reactions from reported placebo-controlled studies and post-marketing experience with JARDIANCE®.
JARDIANCE® (empagliflozin) efficacy

Efficacy

For your patients with CKD: help to reduce the risk of kidney disease progression or CV death in a broad patient population* vs placebo.1,19
JARDIANCE® (empagliflozin) clinical trial

Clinical trial

JARDIANCE® (empagliflozin) was studied in a dedicated CKD SGLT2 inhibitor trial published in The New England Journal of Medicine.19

* EMPA-KIDNEY included patients with a wide range of underlying causes of CKD, many with co-morbidities across the spectrum of cardiovascular, kidney, or metabolic conditions. EMPA-KIDNEY included adult patients with an eGFR ≥20 to <45mL/min/1.73m2 or an eGFR ≥45 to <90mL/min/1.73m2 with a UACR ≥200mg/g, at risk of CKD progression.

Kidney disease progression defined as: adults with kidney function loss (sustained reduction of ≥40% eGFR decline, sustained eGFR <10mL/min/1.73m2), end stage kidney disease (initiation of chronic dialysis or kidney transplant), or renal death.

Abbreviations

CRM: cardio-renal-metabolic; CV: cardiovascular; CKD: chronic kidney disease; HbA1c: glycated haemoglobin; CVD: cardiovascular disease; LV: left ventricular; SGLT2is: sodium-glucose co-transporter-2 inhibitors; T2D: type 2 diabetes mellitus.

References
  1. JARDIANCE® (empagliflozin) Summary of Product Characteristics (SmPC). Available at: http://www.medicines.org.uk/emc/medicine/28973.
  2. Torimoto K et al. Diabetol Metab Syndr. 2017;9:60.
  3. Ferrannini G et al. Diabetes Care. 2015;38:1730–1735.
  4. Ridderstråle M et al. Lancet Diabetes Endocrinol. 2014;2:691–700.
  5. Garg V et al. Prog Cardiovasc Dis. 2019;62:349–357.
  6. Wanner C et al. N Engl J Med. 2016; 375:323–334.
  7. Chilton R et al. Diabetes Obes Metab. 2015;17:1180–1193.
  8. Heise T et al. Clin Ther 2016;38:2265-2276.
  9. Vallon V & Thomson SC. Diabetologia 2017;60:215-225.
  10. Verma S et al. Circulation 2019;140:1693-1702.
  11. Verma S et al. JAMA Cardiol 2017;2:939-940.
  12. Abdelgadir E et al. J Clin Med Res 2018;10:615-625.
  13. Rajasekeran H et al. Kidney Int 2016;89:524-526.
  14. Baartscheer A et al. Diabetologia 2017;60:568-573.
  15. Garg V et al. Prog Cardiovasc Dis 2019;62:349-357.
  16. Zinman B et al. N Engl J Med 2015;373:2117.
  17. Wanner C et al. N Engl J Med 2016;375:323.
  18. Kalra S. Diabetes Ther. 2014 Dec;5(2):355-66.
  19. Herrington WG, et al. N Engl J Med. 2023;388(2):117-127. (EMPA-KIDNEY results and the publication’s Supplementary Appendix).

PC-GB-108940 V2

March 2024

Reporting adverse events

Adverse events should be reported. Reporting form and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (freephone).

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