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Taking people in United StatesPhase 2/3

Tests vericiguat in children with heart failure from weakened heart pumping

Tests vericiguat against a placebo in children with heart failure from weak heart pumping.

Plain-language title generated from the registry record
Registry title: Efficacy, Safety, and Pharmacokinetics of Vericiguat in Pediatric Participants With Heart Failure Due to Left Ventricular Systolic Dysfunction (MK-1242-036)

Key facts

Where
Ann Arbor, Atlanta, Aurora, Boston, Cincinnati, Cleveland, Dallas, Houston, Los Angeles, Memphis, New York, Palo Alto, Philadelphia, Pittsburgh, San Bernardino, Seattle, St Louis, St. Petersburg, The Bronx, and Washington D.C., United StatesSee the 20 sites
Phase
Phase 2/3

Where in United States

  • C.S. Mott Children's Hospital (Site 0033)Ann Arbor, United StatesTaking people
  • Children's Healthcare of Atlanta - Arthur M. Blank Hospital (Site 0001)Atlanta, United StatesTaking people
  • Children's Hospital Colorado (Site 0012)Aurora, United StatesNo longer taking part
  • Boston Children's Hospital (Site 0035)Boston, United StatesTaking people
  • Cincinnati Children's Hospital Medical Center (Site 0034)Cincinnati, United StatesTaking people
  • Cleveland Clinic-Cleveland Clinic Chidren's (Site 0022)Cleveland, United StatesTaking people
  • Children's Health-The Heart Center (Site 0015)Dallas, United StatesTaking people
  • Texas Children's Hospital (Site 0039)Houston, United StatesTaking people
  • The Regents of the University of California - Los Angeles (UCLA Pediatrics) (Site 0002)Los Angeles, United StatesTaking people
  • Le Bonheur Children's Hospital (Site 0007)Memphis, United StatesTaking people
  • Columbia University Medical Center-Pediatric Cardiology (Site 0016)New York, United StatesTaking people
  • Lucile Packard Children's Hospital (Site 0040)Palo Alto, United StatesTaking people
  • Children's Hospital of Philadelphia (CHOP) (Site 0004)Philadelphia, United StatesTaking people
  • Children's Hospital of Pittsburgh (Site 0010)Pittsburgh, United StatesTaking people
  • Loma Linda University Health System (Site 0008)San Bernardino, United StatesTaking people
  • Seattle Children's Hospital-Cardiology/Fetal Therapy (Site 0019)Seattle, United StatesTaking people
  • Washington University-Pediatric Cardiology/ St. Louis Children's Hospital (Site 0006)St Louis, United StatesTaking people
  • Johns Hopkins All Children's Hospital (Site 0029)St. Petersburg, United StatesTaking people
  • The Children's Hospital at Montefiore (Site 0030)The Bronx, United StatesTaking people
  • Children's National Medical Center (Site 0020)Washington D.C., United StatesTaking people

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Trial details

Who runs it
Merck Sharp & Dohme LLC
Trial code
NCT05714085EU 2022-501238-52-00
Record updated
10 November 2026
Original description
This study aims to compare the efficacy of vericiguat versus placebo on change in n-terminal pro-brain natriuretic peptide (NTproBNP) from baseline to Week 16 of the Base Period. The primary hypothesis is that vericiguat is superior to placebo in reducing NT-proBNP at Week 16 of the Base Period.Read full original descriptionShow less

A Phase 2/3 Randomized, Placebo-Controlled, Double-blind, Clinical Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Vericiguat in Pediatric Participants With Heart Failure Due to Systemic Left Ventricular Systolic Dysfunction (VALOR)

This study aims to compare the efficacy of vericiguat versus placebo on change in n-terminal pro-brain natriuretic peptide (NTproBNP) from baseline to Week 16 of the Base Period. The primary hypothesis is that vericiguat is superior to placebo in reducing NT-proBNP at Week 16 of the Base Period.

Inclusion: Has symptomatic chronic heart failure (HF) resulting from systemic left ventricular (LV) systolic dysfunction; Has biventricular physiology with a morphologic systemic left ventricle; Is currently receiving stable medical therapy for HF; Has left ventricular ejection fraction (LVEF) <45% assessed within 3 months before randomization; Is of any sex/gender, from >28 days to <18 years of age inclusive. Must weigh ≥3 kg to participate; Female is eligible to participate if not pregnant or breastfeeding, and at least one of the following: is not a participant of childbearing potential (POCBP); or is a POCBP who uses a highly effective contraceptive method; has a negative highly sensitive pregnancy test; abstains from breastfeeding during the study intervention period and for at least 30 days after study intervention; and their medical history; their menstrual history, and recent sexual activity has been reviewed; Extension Period: Was randomized, received at least 1 dose of study intervention (vericiguat or placebo), did not permanently discontinue study intervention, and completed the Week 52 visit and safety follow-up period of the Base Period.

Exclusion: Has undergone heart transplantation, is awaiting heart transplantation United Network for Organ Sharing (UNOS) Class 1A or equivalent, is receiving continuous IV infusion of an inotrope, or has an implanted ventricular assist device; Has sustained or symptomatic dysrhythmia uncontrolled with drug or device therapy; Has had recent cardiovascular (CV) surgical procedure or percutaneous intervention to palliate or correct congenital CV malformations; Has concurrent or anticipated concomitant use of phosphodiesterase type 5 inhibitors or an sGC stimulator; Has received a COVID-19 vaccination within 1 week before randomization; Has a known allergy or sensitivity to vericiguat, any of its constituents, or any other soluble guanylate cyclase (sGC) stimulator; Has a history of single ventricle heart disease or has a morphologic systemic right ventricle; Has unoperated or residual hemodynamically significant congenital cardiac malformations; Has acute coronary syndrome, undergone recent coronary intervention, or indication for coronary revascularization; Has symptomatic carotid stenosis or other symptomatic cerebrovascular disease; Has severe pulmonary hypertension; Requires continuous home oxygen for significant pulmonary disease and/or has known interstitial lung disease; Has severe chronic kidney disease; Has a gastrointestinal or biliary disorder that could impair absorption, metabolism, or excretion of medications; Has significant bone disease (other than osteopenia) that in the assessment of the investigator can alter bone formation; Has hepatic disorder such as hepatic encephalopathy, hepatic laboratory abnormalities or Child Pugh Class C; Is clinically unstable-with at least one of the following: has symptomatic hypotension or is hypotensive for age, recent use of intravenous (IV) inotrope and/or IV vasodilator, or recent IV diuretic; Has hypertrophic or restrictive cardiomyopathy; Has active myocarditis or has been recently diagnosed with presumed or definitive myocarditis.

ClinicalTrials.gov NCT05714085 · EU CTIS 2022-501238-52-00