Empagliflozin in Heart Failure with Reduced Ejection Fraction and End Stage Renal Disease

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age20+
SponsorNational Taiwan University Hospital

About this trial

In patients with ESRD, up to 20% of patients suffer from HFrEF, leading to significant CV morbidity and mortality. Several drug classes that provide survival benefits for patients with HFrEF, including SGLT2i, lack data regarding their efficacy and safety in patients under chronic hemodialysis. As the primary target of SGLT2i is expressed mostly in the kidneys, the efficacy of SGLT2i in patients with ESRD may be limited. On the other hand, patients with ESRD are at higher risks of experiencing cardiovascular events and may still benefit from treatment. Several mechanistic studies have demonstrated direct actions of SGLT2i on the myocardium, thus it is possible that the benefits of SGLT2i on heart failure are independent of their glycosuric actions and may still be present in anuric subjects. Furthermore, pharmacokinetics and pharmacodynamics studies on empagliflozin demonstrated that peak plasma levels of empagliflozin in subjects with renal failure/ESRD were similar to those in subjects with normal renal function. The use of empagliflozin in patients with ESRD seemed safe in terms of pharmacokinetics and pharmacodynamics, yet its efficacy remains to be explored.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥20 years old

ESRD under chronic, maintenance hemodialysis with stable dry weight for the past 6 months

Documented left ventricular ejection fraction <50% by any imaging modality within 1 month of screening

Disqualifiers

Age <20 years old

Ongoing pregnancy

NYHA class IV heart failure

Any hospitalization for heart failure within the past month

Trial design

Design model

Parallel

Treatments tested in this trial

  • Empagliflozin 25 MG

    Drug

    The medication will be packed in a customized sealed jar and labeled on the exterior of the jar.

  • Placebo

    Drug

    The placebo tablet is manufactured by Prince Pharmaceutical Co., Ltd, a leading manufacturer of nutritional supplements with certifications including cGMP, GMP, ISO, and HACCP. The Prince Pharmaceutical also provides Original Equipment Manufacturing (OEM)/Original Design Manufacturing (ODM) services for a wide array of tablet shapes, and post-processing techniques such as film coating and sugar coating.

Treatment groups

95 Participants
are divided into 2 treatment groups
Group A: empagliflozinExperimental treatment 1 intervention
Group B: placeboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Left ventricular mass

As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day

Time frame
24 weeks of treatment

Secondary outcomes

1

Left ventricular mass index

As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day

Time frame
24 weeks of treatment
2

LV end-systolic volume index

As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day

Time frame
24 weeks of treatment
3

LV end-diastolic volume index

As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day

Time frame
24 weeks of treatment
4

LA volume index

As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day

Time frame
24 weeks of treatment

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

National Taiwan University Hospital

Lead sponsor

Shin Kong Wu Ho-Su Memorial Hospital

Collaborator