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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT04788511




Registration number
NCT04788511
Ethics application status
Date submitted
5/03/2021
Date registered
9/03/2021

Titles & IDs
Public title
Research Study to Investigate How Well Semaglutide Works in People Living With Heart Failure and Obesity
Scientific title
Effect of Semaglutide 2.4 mg Once Weekly on Function and Symptoms in Subjects With Obesity-related Heart Failure With Preserved Ejection Fraction
Secondary ID [1] 0 0
U1111-1243-4358
Secondary ID [2] 0 0
EX9536-4665
Universal Trial Number (UTN)
Trial acronym
STEP-HFpEF
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Obesity 0 0
Condition category
Condition code
Cardiovascular 0 0 0 0
Coronary heart disease
Cardiovascular 0 0 0 0
Other cardiovascular diseases
Diet and Nutrition 0 0 0 0
Obesity
Metabolic and Endocrine 0 0 0 0
Other metabolic disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Semaglutide
Treatment: Drugs - Placebo (semaglutide)

Experimental: Semaglutide - All participants will receive either semaglutide 2.4 mg once weekly or placebo once weekly as add-on to standard of care. During the first 16 weeks, the dose of semaglutide or placebo will be gradually escalated from 0.25 mg once weekly until target dose.

Placebo comparator: Placebo (semaglutide) - All participants will receive either semaglutide 2.4 mg once weekly or placebo once weekly as add-on to standard of care. During the first 16 weeks, the dose of semaglutide or placebo will be gradually escalated from 0.25 mg once weekly until target dose.


Treatment: Drugs: Semaglutide
Semaglutide will be injected into a skin fold, in the stomach, thigh or upper arm once a week at the same day of the week (to the extent possible) throughout the trial.

Dose gradually escalated from 0.25 mg until target dose. The study will last for approximately 59 weeks.

Treatment: Drugs: Placebo (semaglutide)
Placebo will be injected into a skin fold, in the stomach, thigh or upper arm once a week at the same day of the week (to the extent possible) throughout the trial.

The study will last for approximately 59 weeks.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change in Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (KCCQ-CSS)
Timepoint [1] 0 0
From baseline (week 0) to end of treatment (week 52)
Primary outcome [2] 0 0
Change in Body Weight
Timepoint [2] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [1] 0 0
Change in Six-minute Walking Distance (6MWD)
Timepoint [1] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [2] 0 0
The Hierarchical Composite Endpoint: Percentage of Wins of Participant Pairs
Timepoint [2] 0 0
From baseline (week 0) to end of study (week 57)
Secondary outcome [3] 0 0
Change in C-Reactive Protein (CRP): Ratio to Baseline
Timepoint [3] 0 0
From baseline (week -2) to end of treatment (week 52)
Secondary outcome [4] 0 0
Percentage of Participants Achieving 10 Percent (%) Weight Loss (Yes/No)
Timepoint [4] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [5] 0 0
Percentage of Participants Achieving 15% Weight Loss (Yes/No)
Timepoint [5] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [6] 0 0
Percentage of Participants Achieving 20% Weight Loss (Yes/No)
Timepoint [6] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [7] 0 0
Percentage of Participants Improving 5 Points or More in KCCQ Clinical Summary Score (Yes/No)
Timepoint [7] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [8] 0 0
Percentage of Participants Improving 10 Points or More in KCCQ Clinical Summary Score (Yes/No)
Timepoint [8] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [9] 0 0
Change in KCCQ Overall Summary Score (KCCQ-OSS)
Timepoint [9] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [10] 0 0
Percentage of Participants Achieving Threshold for Clinically Meaningful Within-participants Change in KCCQ-CSS (PGI-S)
Timepoint [10] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [11] 0 0
Percentage of Participants Achieving Threshold for Clinically Meaningful Within-participants Change in 6MWD (PGI-S)
Timepoint [11] 0 0
From baseline (week 0) to end of treatment (week 52)
Secondary outcome [12] 0 0
Change in Systolic Blood Pressure (SBP)
Timepoint [12] 0 0
From baseline (week -2) to end of treatment (week 52)
Secondary outcome [13] 0 0
Change in Waist Circumference
Timepoint [13] 0 0
From baseline (week 0) to end of treatment (visit 52)

Eligibility
Key inclusion criteria
* Male or female, age above or equal to 18 years at the time of signing informed consent.
* Body mass index (BMI) greater than or equal to 30.0 kg/m^2
* New York Heart Association (NYHA) Class II-IV
* Left ventricular ejection fraction (LVEF) greater than or equal to 45 percentage at screening
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* A self-reported change in body weight greater than 5 kg (11 lbs) within 90 days before screening irrespective of medical records
* Haemoglobin A1c (HbA1c) greater than or equal to 6.5 percentage (48 mmol/mol) based on latest available value from medical records, no older than 3 months or if unavailable a local measurement at screening

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
16/03/2021
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
18/04/2023
Sample size
Target
Accrual to date
Final
529
Recruitment in Australia
Recruitment state(s)
ACT,NSW,SA,VIC
Recruitment hospital [1] 0 0
The Canberra Hospital_Garran - Garran
Recruitment hospital [2] 0 0
Concord Repatriation General Hospital - Cardiology - Concord
Recruitment hospital [3] 0 0
Liverpool Hospital - Liverpool
Recruitment hospital [4] 0 0
Flinders Medical Centre - Bedford Park
Recruitment hospital [5] 0 0
Geelong Cardiology Research Unit - Geelong
Recruitment postcode(s) [1] 0 0
2605 - Garran
Recruitment postcode(s) [2] 0 0
2139 - Concord
Recruitment postcode(s) [3] 0 0
2170 - Liverpool
Recruitment postcode(s) [4] 0 0
5042 - Bedford Park
Recruitment postcode(s) [5] 0 0
3220 - Geelong
Recruitment outside Australia
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United States of America
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Alabama
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Illinois
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Caba
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Hardenberg
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Lodzkie
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Gdynia
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Valencia
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Dundee
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Glasgow
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High Wycombe
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Liverpool
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Manchester
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Swindon
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West Sussex

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Novo Nordisk A/S
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Clinical Transparency (dept. 1452)
Address 0 0
Novo Nordisk A/S
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
According to the Novo Nordisk disclosure commitment on novonordisk-trials.com
When will data be available (start and end dates)?
Available to whom?
Available for what types of analyses?
How or where can data be obtained?
IPD available at link: http://novonordisk-trials.com


What supporting documents are/will be available?




Results publications and other study-related documents

TypeCitations or Other Details
Journal Kosiborod MN, Abildstrom SZ, Borlaug BA, Butler J,... [More Details]


Results are available at https://clinicaltrials.gov/study/NCT04788511