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Life sciences · Phase 1 Trial
ClinicalTrials.gov · October 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07219511). This is a study registration, not published results. Lead sponsor: Vasa Therapeutics. Recruitment status: ACTIVE_NOT_RECRUITING. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 42 participants (ESTIMATED). Conditions: Heart, Heart Failure With Preserved Ejection Fraction (HFPEF). Interventions: DRUG: VS-041; OTHER: Placebo. Primary outcome measures: Participant incidence of treatment-emergent adverse events (TEAEs) , From Baseline to Day 28; Change from baseline over time in serum NordicPRO-C6 , From Baseline to Day 28; Change from baseline over time in serum endotrophin , From Baseline to Day 28; Change from baseline over time in serum NT-proBNP , From Baseline to Day 28. Brief summary: A Safety, Tolerability, and Biomarker Trial of VS-041 in Participants with Heart Failure with Preserved Ejection Fraction (HFpEF)