Clin2
NCT05321875Possibly a fitRecruiting

Candesartan to prevent heart failure in certain gene carriers

Cardiomyopathy, Dilated

Treatments studied

Part of Genetic & congenital, Heart & circulation clinical trials.

This trial tests whether candesartan (a blood-pressure medicine) can delay or prevent heart muscle weakening in people who carry a disease-causing dilated cardiomyopathy gene variant but still have fairly strong heart pumping. Participants are randomly assigned to candesartan or a placebo to see which one keeps the heart healthier over time.

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

Phase
Phase 3
Enrollment
320 people
Ages
18 years to 64 years
Study type
Interventional

Who can take part

  • You are 18–64 years old and can legally consent
  • You carry a pathogenic or likely pathogenic dilated cardiomyopathy gene variant
  • Your heart pumping strength is preserved (left ventricle ejection fraction 50% or higher) on a heart MRI
  • Your kidney blood tests are acceptable (creatinine ≤ 1.3, potassium ≤ 5.3, and eGFR ≥ 60)
  • Your blood pressure is not too low (systolic must be 100 or higher) and not uncontrolled high
  • You are able and willing to get MRI scans and take the study medicine/placebo safely

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.

Similar studies

Other trials that look related to this one.

NCT06091475Recruiting
Maintaining remission in improved dilated cardiomyopathy

This study tests whether people with dilated cardiomyopathy whose heart function has already recovered to normal can safely stop or reduce one of their heart medications while staying in remission. It aims to find the best way to keep the heart healthy without extra medicines.

London
NCT06712030Not yet recruiting· Phase 3
Heart drug study for amyloidosis with low pumping strength

This test looks at sacubitril/valsartan — a heart failure pill — in people who have a type of amyloidosis that affects the heart (called ATTR amyloidosis) and who also have a heart that pumps weakly (ejection fraction 40% or less). The goal is to see if it helps heart function and daily life.

Majadahonda, Madrid
NCT07210723Recruiting· Phase 2/Phase 3
Study of danicamtiv for genetic and familial dilated cardiomyopathy

This trial tests if danicamtiv can improve heart function in people with dilated cardiomyopathy caused by certain genetic changes. It may help those who have stable symptoms but still need more treatment options.

Birmingham, Alabama
NCT07771465Not yet recruiting· Phase 3
Long-term safety of danicamtiv for genetic dilated cardiomyopathy

This study checks the long-term safety and effectiveness of the drug danicamtiv in people with a genetic form of dilated cardiomyopathy, a condition where the heart muscle becomes weak and enlarged. If you've already completed the earlier DAN-301 study, this trial continues to monitor you while you keep taking the medication.

Birmingham, Alabama
NCT07415642Not yet recruiting
Medication and ICDs for dilated cardiomyopathy

This trial tests whether combining modern heart failure medications with an implantable defibrillator (ICD) can reduce the risk of dangerous heart rhythms and improve survival in people with dilated cardiomyopathy. It focuses on those with a weak heart pump and specific scarring seen on MRI.

Groningen
NCT06632834Recruiting· Phase 2
Targeted treatment study for dilated cardiomyopathy

This study tests whether a personalized treatment approach can improve heart function in people with dilated cardiomyopathy (a condition where the heart becomes enlarged and weak). It focuses on patients who still have low heart function despite standard medications.

Taipei County, Zhongzheng District

Hear when a new Cardiomyopathy, Dilated trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.