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Trial · Observational

CompletedPhase not statedRegistry data

Emulation of the STEP-HFpEF DM Heart Failure Trial in Healthcare Claims Data

Short name DUP-STEP-HFpEF

NCTNCT06914102 (opens ClinicalTrials.gov in a new tab)Other id2018P002966-DUP-STEP-HFpEF

Overview

Status
Completed
Phase
Phase not stated
Enrollment
58,387 participants (actual)
Sponsor
Brigham and Women's Hospital · Other
Design
Not stated
Countries
1 country

United States

Start
14 Jan 2025
Primary completion
1 Jun 2025
Completion
1 Jun 2025
First posted
6 Apr 2025
Last update posted
30 Jan 2026
Conditions
Diabetes Mellitus, Type 2 · HFpEF - Heart Failure With Preserved Ejection Fraction

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
20252026
  1. Ph –

    DUP-STEP-HFpEF

    NCT06914102

    14 Jan 2025 to 1 Jun 2025

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

Investigators are building an empirical evidence base for real-world data through large-scale emulation of randomized controlled trials. The investigators' goal is to understand for what types of clinical questions real world data analyses can be conducted with confidence and how to implement such studies.

Interventions

  • SemaglutideDrug
  • PlaceboDrug

Arms2

  • Other

    Semaglutide

    Exposure group

  • Other

    Placebo

    Reference group

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Composite of all-cause mortality or heart failure hospitalization

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on composite of all-cause mortality or heart failure hospitalization in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

Secondary outcomes(8)
  1. Composite of all-cause mortality or a worsening heart failure event (exacerbated symptoms of heart failure resulting in hospitalization, intravenous diuretic therapy in an urgent care setting), and its respective individual end points.

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on composite of all-cause mortality or all-cause mortality or a worsening heart failure event (exacerbated symptoms of heart failure resulting in hospitalization, intravenous diuretic therapy in an urgent care setting) in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

  2. Worsening heart failure event (exacerbated symptoms of heart failure resulting in hospitalization or intravenous diuretic therapy in an urgent care setting)

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on worsening heart failure event (exacerbated symptoms of heart failure resulting in hospitalization or intravenous diuretic therapy in an urgent care setting) in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

  3. Intravenous diuretic therapy in an urgent care setting

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on intravenous diuretic therapy in an urgent care setting in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

  4. Hospitalization for heart failure

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on hospitalization for heart failure in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

  5. All-cause mortality

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on all-cause mortality in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

  6. Urinary tract infection

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on urinary tract infection in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

  7. Serious bacterial infection

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semgalutide vs placebo (sitaglitpin) on serious bacterial infection in two populations (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

  8. Gastrointestinal adverse events

    Time frame · Through study completion (1 day after cohort entry date until the first of outcome or censoring)

    Registry description

    To evaluate the effect of semaglutide vs placebo (sitagliptin) on gastrointestinal adverse events in two populations: (1) patients meeting the eligibility criteria of the STEP-HFpEF DM trial, and (2) a broader patient population when relaxing the eligibility criteria of the STEP-HFpEF DM trial.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

Completed trials do not always post results.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Observational study · 2025

5 results

Semaglutide and Tirzepatide in Patients With Heart Failure With Preserved Ejection Fraction.

Krüger et al. 2025JAMAcited by 43

PMID 40886075PMC12400167DOI 10.1001/jama.2025.14092PUB-40886075

Rights unknown5 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Eligible cohort entry dates: Optum: Study period between January 1, 2018 to November 30, 2024. Marketscan: Study period between January 1, 2018 to December 31, 2023. Medicare: Study period between January 1, 2018 to December 31, 2020. FOLLOWING ELIGIBILITY OF THE STEP-HFpEF DM TRIAL Inclusion Criteria: * Male or female, age above or equal to 18 years at the time of signing informed consent. * BMI ≥ 30.0 kg/m2 * NYHA Class II-IV * LVEF ≥ 45% * No hospitalizations due to heart failure between screening (V1) and randomization (V2) * At least one of the following: * If BMI \<35.0: NT-proBNP ≥ 220 pg/mL (for patients with sinus rhythm) or NTproBNP ≥660 pg/mL (for patients with persistent/permanent atrial fibrillation); if BMI ≥ 35.0: NT-proBNP ≥ 125 pg/mL (for patients with sinus rhythm) or NTproBNP ≥ 375 pg/mL (for patients with persistent/permanent atrial fibrillation) at screening (NT-proBNP analyzed by the central laboratory) in combination with at least one of the following (documented by echocardiography within 12 months prior to or at screening): i. Septal é \< 7cm/sec or lateral é \< 10 cm/sec or average E/é ≥ 15 ii. PA systolic pressure \>35mmHg iii. Left atrial (LA) enlargement (LA width ≥3.8 cm or LA length ≥ 5.0cm or LA area ≥ 20.0cm2 or LA volume ≥ 55mL or LA volume index ≥29mL/m2) iv. LV hypertrophy with septal thickness or posterior wall thickness ≥1.2cm * Hospitalization with a primary diagnosis of decompensated heart failure which required intravenous loop diuretic treatment, within the previous 12 months in combination with at least two of the following (documented by echocardiography within 12 months prior to or at screening): i. Septal é \< 7cm/sec or lateral é \< 10cm/sec or average E/é ≥15 ii. PA systolic pressure \>35mmHg iii. LA enlargement (LA width ≥3.8cm or LA length ≥ 5.0cm or LA area ≥20.0cm2 or LA volume ≥ 55mL or LA volume index ≥ 29mL/m2) iv. LV hypertrophy with septal thickness or posterior wall thickness ≥1.2cm * Diagnosed with T2D ≥ 90 days prior to the day of screening. * Subject treated with diet, exercise, and/or antidiabetic treatment\* according to local label in stable dosing for at least 30 days prior to screening: o \*OAD(s): unchanged drug(s), dose and dosing frequency o \*Insulin(s): unchanged regimen (basal, basal + bolus, premix combination) with stable total daily insulin dose as judged by the investigator Exclusion Criteria: * Myocardial infarction, stroke, hospitalization for heart failure, unstable angina pectoris or transient ischemic attack within 30 days prior to the day of screening. * Systolic blood pressure \> 160 mmHg at screening. * Any other condition judged by the investigator to be the primary cause of dyspnea (such as heart failure due to restrictive cardiomyopathy or infiltrative conditions (e.g. amyloidosis), hypertrophic obstructive cardiomyopathy, primary pulmonary arterial hypertension, chronic obstructive pulmonary disease, right heart failure due to pulmonary disease, complex congenital heart disease, anemia, or more than moderate heart valve disease). * Bariatric surgery prior to screening or planned bariatric surgery within the trial time course. * History of type 1 diabetes (history of gestational diabetes is allowed). * Treatment with any GLP-1 receptor agonist within 90 days prior to the day of screening. * Uncontrolled and potentially unstable diabetic retinopathy or maculopathy. * Recurrent severe hypoglycemic episodes within the last year as judged by the investigator. * Treatment with continuous subcutaneous insulin infusion * Personal or first-degree relative(s) history of multiple endocrine neoplasia type 2 or medullary thyroid carcinoma. * Presence of acute pancreatitis within the last 180 days prior to screening. * History or presence of chronic pancreatitis. * End-stage renal disease or chronic or intermittent hemodialysis or peritoneal dialysis. * Presence or history of malignant neoplasm within 5 years prior to the day of screening. Basal and squamous cell cancer and any carcinoma in-situ are allowed. * Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using a highly effective contraceptive method. * Any disorder, including severe psychiatric disorder, suicidal behavior within 90 days before screening, and suspected drug abuse, which in the investigator´s opinion might jeopardize subject´s safety or compliance with the protocol. RELAXING ELIGIBILITY OF THE STEP-HFpEF DM TRIAL Inclusion Criteria: * Men or women ≥ 18 years old * History of type 2 diabetes mellitus * BMI ≥ 27.0 kg/m2 * Heart failure * Preserved ejection fraction Exclusion Criteria: * Prior treatment with any GLP-1-RA * History of type 1 diabetes mellitus * End-stage renal disease or chronic or intermittent hemodialysis or peritoneal dialysis * History of bariatric surgery * History of nursing home admission * Pregnant female or breast-feeding * Uncontrolled and potentially unstable diabetic retinopathy or maculopathy * Treatment with continuous subcutaneous insulin infusion * Multiple endocrine neoplasia type 2 or medullary thyroid carcinoma * Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy (other than basal- or squamous-cell skin cancer, in situ carcinoma of the cervix, or in situ prostate cancer) for less than 5 years

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