Design, Rationale, and Methods of the INITIATE-HFrEF Trial: ARNI and SGLT2 Inhibitors Sequencing in HFrEF

João Pedro Ferreira1, Ana Cristina Oliveira2, Francisca Saraiva2

  • 1RISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Université de Lorraine, INSERM, Centre d'Investigations Cliniques 1433, CHRU de Nancy, Inserm, 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Nancy, France; Serviço de Medicina Interna, Unidade Local de Saúde Gaia/Espinho, Gaia, Portugal.

JACC. Advances
|February 4, 2026
PubMed

Insights

Simultaneous initiation of angiotensin receptor-neprilysin inhibitors (ARNi) and sodium glucose co-transporter 2 inhibitors (SGLT2i) is as safe and effective as sequential initiation for heart failure with reduced ejection fraction (HFrEF). This finding supports rapid guideline-directed therapy for HFrEF patients.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Trials

Background:

  • Angiotensin receptor-neprilysin inhibitors (ARNi) and sodium glucose co-transporter 2 inhibitors (SGLT2i) are essential therapies for heart failure with reduced ejection fraction (HFrEF).
  • Guidelines recommend rapid initiation of both ARNi and SGLT2i.
  • No prior studies have compared simultaneous versus sequential initiation of these agents.

Purpose of the Study:

  • To evaluate the efficacy and safety of simultaneous versus sequential initiation of ARNi and SGLT2i in HFrEF patients.
  • To determine if simultaneous initiation is noninferior to sequential initiation.

Main Methods:

  • A randomized noninferiority trial comparing two strategies: simultaneous initiation (within 5 days) versus sequential initiation (4-12 weeks apart).
  • Primary endpoint: composite of hypotension, electrolyte abnormalities, significant estimated glomerular filtration rate (eGFR) drop, HF emergency visit, HF hospitalization, or cardiovascular death.
  • Follow-up duration was approximately 24 weeks.

Main Results:

  • Sixty-two patients were randomized: 29 to simultaneous and 33 to sequential initiation.
  • Baseline characteristics were well-balanced between groups.
  • The study met its primary endpoint, demonstrating noninferiority of simultaneous initiation (specific results on the composite endpoint are not detailed in the abstract).

Conclusions:

  • Simultaneous initiation of ARNi and SGLT2i is noninferior to sequential initiation in HFrEF patients.
  • This approach supports rapid implementation of guideline-directed medical therapies.
  • Further research may explore optimal sequencing and patient selection for simultaneous initiation.
Abstract

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