A Study of VS-041 for Heart Failure with Preserved Ejection Fraction (HFpEF)

This study is testing a medication called VS-041 in people with heart failure with preserved ejection fraction (HFpEF). HFpEF is a type of heart failure where the heart can pump blood normally, but it's too stiff to fill properly. The study aims to understand the safety and how well VS-041 is tolerated at different doses (high and low), compared to a placebo (an inactive pill). Researchers will also look at how the medication affects certain markers in your blood. You may be able to join if you are 50 years or older and have been diagnosed with HFpEF, with symptoms that are mild to moderate (NYHA Functional Class II or III). The study plans to enroll 42 participants.

Study design
This interventional study will involve 42 participants who will receive either a high dose of VS-041, a low dose of VS-041, or a placebo twice a day.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Researchers will monitor participants for adverse events and changes in blood markers from when they start the study until Day 28.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07219511

A Safety, Tolerability, and Biomarker Trial of VS-041 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)

Recruiting
PHASE1Ages 50+InterventionalTreatment
Vasa Therapeutics
~42 participants
Updated 2026-04-09 on ClinicalTrials.gov
What's tested:VS-041Placebo

At a glance

Recruiting sites
19 of 21 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Participant incidence of treatment-emergent adverse events (TEAEs)
Measured over From Baseline to Day 28
+3 more outcomes measured
Heart
Heart Failure With Preserved Ejection Fraction (HFPEF)
21 sites across 12 states
Florida4
California3
Illinois3
North Carolina2
Texas2
Arkansas1
Louisiana1
Missouri1

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  • Participant incidence of treatment-emergent adverse events (TEAEs)From Baseline to Day 28

    To evaluate the safety and tolerability of VS-041 in participants with HFpEF

  • Change from baseline over time in serum NordicPRO-C6From Baseline to Day 28

    To evaluate the impact of VS-041 on key biomarkers in participants with HFpEF

  • Change from baseline over time in serum endotrophinFrom Baseline to Day 28

    To evaluate the impact of VS-041 on key biomarkers in participants with HFpEF

  • Change from baseline over time in serum NT-proBNPFrom Baseline to Day 28

    To evaluate the impact of VS-041 on key biomarkers in participants with HFpEF