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NCT07192952Possibly a fitRecruiting

Long-term safety of finerenone in children and young adults with heart failure

Left Ventricular Systolic DysfunctionHeart Failure (Pediatric)

Treatments studied

Part of Heart & circulation clinical trials.

This study tests the long-term safety of the drug finerenone when taken alongside standard heart failure treatments in children and young adults with weakened heart pumping function (left ventricular systolic dysfunction). It includes both children already in a related study and new infants under 6 months old.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
117 people
Ages
Up to 18 years
Study type
Interventional

Who can take part

  • You or your child must have heart failure with a weakened left heart pump (left ventricular systolic dysfunction).
  • For new infants under 6 months: A heart test (echocardiogram) shows a pumping strength of 50% or less.
  • For new infants under 6 months: A blood test shows high NT-proBNP (a heart strain marker).
  • New infants under 6 months must weigh at least 3 kg (about 6.6 pounds).
  • No use of certain heart medications (spironolactone or eplerenone) within the last 30 days.
  • No serious heart rhythm problems, need for a breathing machine, or IV heart support in the last 30 days.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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