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JARDIANCE® (empagliflozin)
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JARDIANCE® (empagliflozin)
JARDIANCE® (empagliflozin)
JARDIANCE® (empagliflozin)
JARDIANCE® (empagliflozin)
JARDIANCE® (empagliflozin)
JARDIANCE® (empagliflozin)
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JARDIANCE® (empagliflozin)

JARDIANCE® for
SYMPTOMATIC CHRONIC
HEART FAILURE

Learn about JARDIANCE® for the treatment of symptomatic CHF in adult patients including product overview, clinical studies, efficacy and safety profile

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Licensed indications
JARDIANCE® (empagliflozin) chronic heart failure banner
JARDIANCE® (empagliflozin) clinical studies and efficacy

EMPEROR-Reduced trial

Learn more about the EMPEROR-Reduced trial.
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JARDIANCE® (empagliflozin) clinical studies and efficacy

EMPEROR-Preserved trial

Learn more about the EMPEROR-Preserved trial.
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The ESC defined types of heart failure

Each type has different characteristics and is managed differently5

ESC defined types of heart failure
ESC defined types of heart failure

EMPEROR-Reduced trial1

The EMPEROR-Reduced trial investigated the efficacy of empagliflozin 10 mg versus placebo, in addition to guideline-directed medical therapy (GDMT), in patients with symptomatic chronic heart failure with reduced ejection fraction (LVEF ≤40%).

EMPEROR-Reduced trial study design
EMPEROR-Reduced trial study design

Tolerability profile

Selected adverse events in the EMPEROR-Reduced® trial.

JARDIANCE® (empagliflozin) for chronic heart failure: tolerability table
JARDIANCE® (empagliflozin) for chronic heart failure: tolerability table

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* Hypoglycemic AEs with a plasma glucose value of ≤70 mg/dL or that required assistance.

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  • Study Design
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Efficacy results: EMPEROR-Reduced trial

Primary outcome of the EMPEROR-Reduced trial

JARDIANCE® demonstrated superiority in reducing the risk of CV death or HHF in HF patients with LVEF ≤40% on top of SoC vs placebo1,11

The EMPEROR-Reduced trial demonstrated that treatment with JARDIANCE® (empagliflozin) reduced the risk of cardiovascular (CV) death or hospitalization for heart failure (HHF) compared to placebo in patients with heart failure and reduced ejection fraction (LVEF ≤40%). The primary composite endpoint showed a 25% relative risk reduction (RRR) and a 5.3% absolute risk reduction (ARR) in CV death or HHF (HR: 0.75; 95% CI: 0.65–0.86; p<0.001). The number needed to treat (NNT) to prevent one primary event over a 16-month period was 20 (95% CI: 13, 37).

JARDIANCE® (empagliflozin) efficacy graph
JARDIANCE® (empagliflozin) efficacy graph

Secondary outcome of the EMPEROR-Reduced trial

JARDIANCE® reduced total hospital admissions for heart failure in HF patients with LVEF ≤40% on top of SoC vs placebo1,11

The total number of hospitalisations for heart failure was lower in the JARDIANCE® group than in the placebo group, with 388 events vs 553 events, respectively HR, 0.70; 95% CI, 0.58 to 0.85; p<0.001.

Based on the 30% RRR (8.8% ARR) demonstrated for hospitalisations for heart failure, 12 patients would need to have been treated with JARDIANCE® to prevent one event.

JARDIANCE® (empagliflozin) efficacy graph
JARDIANCE® (empagliflozin) efficacy graph

EMPEROR-Preserved trial2

The EMPEROR-Preserved trial investigated the efficacy of empagliflozin 10 mg versus placebo, in addition to background treatment, in patients with symptomatic chronic heart failure with preserved ejection fraction (LVEF >40%).

EMPEROR-Preserved trial study design
EMPEROR-Preserved trial study design

Tolerability profile

Selected adverse events in the EMPEROR-Preserved® trial.

JARDIANCE® (empagliflozin) for chronic heart failure: tolerability table
JARDIANCE® (empagliflozin) for chronic heart failure: tolerability table

* Hypoglycemic AEs with a plasma glucose value of ≤70 mg/dL or that required assistance.

Safety information

Quick navigation

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  • Study Design
  • Tolerability profile

Efficacy results: EMPEROR-Preserved trial

Primary outcome of EMPEROR-Preserved

JARDIANCE® demonstrated superiority in reducing the risk of CV death or HHF in HF patients with LVEF >40% on top of SoC vs placebo1,11

Subgroup analysis showed efficacy was consistent across the spectrum of LVEF.14 The primary composite outcome occurred in 415 patients (13.8%) in the empagliflozin group and 511 patients (17.1%) in the placebo group (HR 0.79; 95% CI, 0.69–0.90; p<0.001).

With a 21% relative risk reduction (3.3% absolute risk reduction) in CV death or hospitalisation for heart failure (HHF), the number needed to treat (NNT) to prevent one primary event was 31 (95% CI, 20–69).

JARDIANCE® (empagliflozin) efficacy graph
JARDIANCE® (empagliflozin) efficacy graph

Secondary composite outcome of EMPEROR-Preserved

JARDIANCE® demonstrated superiority in reducing the risk of first or recurrent HHF in HF patients with LVEF >40% vs placebo.2

The total number of HHF was lower in the JARDIANCE® group than in the placebo group, with 407 events vs 541 events, respectively (HR, 0.73; 95% CI, 0.61 to 0.88; p<0.001).

Based on the 27% RRR (4.5% ARR) demonstrated for HHF, 22 patients would need to have been treated with JARDIANCE® to prevent one event.

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JARDIANCE® (empagliflozin) efficacy graph
JARDIANCE® (empagliflozin) efficacy graph

Knowledge base

JARDIANCE® (empagliflozin) dosing
Dose & Administration

JARDIANCE® is simple to initiate at 10 mg dosing across all indications. 

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JARDIANCE® (empagliflozin) safety
Safety Profile

Adverse reactions from reported placebo-controlled studies and post-marketing experience.

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JARDIANCE® (empagliflozin) events
Events

Explore upcoming stands and symposiums where the JARDIANCE® team will be present

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JARDIANCE® (empagliflozin) resources
Resources

Helpful resources supporting you every step of the way.


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Abbreviations

3P-MACE: 3-point major adverse cardiovascular events; AE: adverse event; ARR: absolute risk reduction; CHF: chronic heart failure; CI: confidence interval; CV: cardiovascular; HHF: hospitalisation due to heart failure; CVD: cardiovascular disease; DPP-4: dipeptidyl-peptidase 4; EASD: European Association for the Study of Diabetes; eGFR: estimated glomerular filtration rate; ESC: European Society of Cardiology; HF: heart failure; HFmrEF: heart failure with mildly reduced ejection fraction; HFpEF: heart failure with preserved ejection fraction; HFrEF: heart failure with reduced ejection fraction; HHF: hospitalisation for heart failure; HR: hazard ratio; KCCQ: Kansas City Cardiomyopathy Questionnaire; LVEF: left ventricular ejection fraction; MACE: major adverse cardiac events; MI: myocardial infarction; NEJM: New England Journal of Medicine; NT-proBNP: N-terminal pro hormone B-type natriuretic peptide; NYHA: New York Heart Association; RRR: relative risk reduction; T2D: type 2 diabetes.

  1. Packer M, et al. N Engl J Med. 2020;383(15):1413-1424. (& Supplementary appendix).
  2. Anker SD, et al. N Engl J Med. 2021;385(16):1451–1461.
  3. Butler J, et al. Eur Heart J. 2021;42:1203–1212.
  4. Butler J, et al. Circulation. 2022;145:184–193.
  5. McDonagh TA, et al. Eur Heart J. 2021;42(36):3599–3726.
  6. Kemp CD, Conte JV. Cardiovasc Pathol. 2012;21:365–371.
  7. Zhou Q, et al. Front Cardiovasc Med. 2021;8:678121.
  8. Obokata M, et al. JACC Cardiovasc Imaging. 2020;13(1 Pt 2):245–257.
  9. Bohm M, et al. J Am Coll Cardiol. 2022;80:1–18.
  10. Zinman B, et al. N Engl J Med. 2015;373:2117–2128.
  11. JARDIANCE® (empagliflozin) Summary of Product Characteristics (SmPC). Available at: http://www.medicines.org.uk/emc/medicine/28973.
  12. Packer M et al. Circulation 2021;143(4)326–336 and supplementary appendix.
  13. Butler J, et al. Eur J Heart Failure. 2022;24:245–248.
  14. Anker SD, et al. Nat Med. 2022;28:2512–2520.

PC-GB-110621 | December 2024

Reporting adverse events

Adverse events should be reported. Reporting forms 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).

Please be aware that this website contains promotional information about Boehringer Ingelheim medicines and services. Some of this may not be directly relevant to your scope of practice and it is your own decision whether you choose to view this information.

Disclaimer

The content on this website is in relation to adult patients.

Empagliflozin is not recommended in severe hepatic impairment, breastfeeding, Type 1 diabetes and is contraindicated in patients with hypersensitivity to the active ingredient or any of its excipients. Empagliflozin should be avoided in pregnancy.

Please consult the SmPC for full details regarding adverse events, monitoring requirements and interactions prior to prescribing JARDIANCE®.

  1. JARDIANCE® (empagliflozin) UK Summary of Product Characteristics (SmPC). Available at:
    http://www.medicines.org.uk/emc/medicine/28973.
Indications

JARDIANCE® is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise

  • as monotherapy when metformin is considered inappropriate due to intolerance
  • in addition to other medicinal products for the treatment of diabetes1

JARDIANCE® is indicated in adults for the treatment of chronic kidney disease.1

JARDIANCE® is indicated in adults for the treatment of symptomatic chronic heart failure.1

PC-GB-109995 V4 | October 2025

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