JARDIANCE® (Empagliflozin)

The content on this website is in relation to adult patients

 

EMPA-KIDNEY Trial

The largest dedicated CKD SGLT2i trial to date1-3,6

JARDIANCE was evaluated in a broad patient population vs placebo1. 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.

EMPA-KIDNEY trial study design

Patient characteristics at baseline (N=6609)1

Patient characteristics at baseline (N=6609)

History of diabetes defined as self-reported history of diabetes of any type, use glucose-lowering medication, or HbA1c ≥48mmol/mol (6.5%) at randomisation.

Prior CV disease defined as self reported history of myocardial infarction, heart failure, stroke, TIA or PAD.

EMPA-KIDNEY is the only SGLT2i CKD trial to include the understudied type of patients with low eGFR and without albuminuria1-3,6

Moa diagram t2d

* Defined as low risk if there are no other markers of kidney disease or CKD.

Abbreviations

CKD: chronic kidney disease; CV: cardiovascular; CVD: cardiovascular disease; DKD: diabetic kidney disease; eGFR: estimated glomerular filtration rate; HbA1c: glycated haemoglobin; IgA: immunoglobulin A; PAD: peripheral arterial disease; RAASi: renin-angiotensin-aldosterone system inhibitor; SGLT2i: sodium-glucose co-transporter-2 inhibitor; T2D: type 2 diabetes mellitus; TIA: transient ischaemic attack; UACR: urinary albumin-to-creatinine ratio.

References
  1. Herrington WG, et al. N Engl J Med. 2023;388(2):117-127. (EMPA-KIDNEY results and the publication’s Supplementary Appendix).
  2. Heerspink H, et al. N Engl J Med. 2020;383:1436-1446.
  3. Perkovic V, et al. N Engl J Med. 2019;380:2295-2306.
  4. EMPA-KIDNEY Collaborative Group. Nephrol Dial Transplant 2022;371317-1329.
  5. Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. Kidney Int Suppl 2013;3:1.
  6. JARDIANCE Data on File (EMP 23-29).

PC-GB-108943 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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