Finerenone for Heart Failure

(FIORELLO Trial)

Not yet recruiting at 136 trial locations
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores the safety and effectiveness of finerenone for treating heart failure in children and young adults, particularly those with left ventricular systolic dysfunction, where the heart struggles to pump blood effectively. Finerenone blocks a protein that can cause inflammation and scarring in the heart, potentially improving heart function. The trial includes newborns and infants under six months with heart failure and those who participated in a previous study called FIORE. Children and young adults with heart failure symptoms like shortness of breath or fatigue, already receiving standard heart failure treatment, might be suitable candidates. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to a potentially groundbreaking treatment.

Do I need to stop my current medications to join the trial?

Participants can continue their standard heart failure treatments while taking finerenone in the study. However, they must not take other mineralocorticoid receptor antagonists like spironolactone or eplerenone within 30 days before starting the trial.

Is there any evidence suggesting that finerenone is likely to be safe for children and young adults with heart failure and LVSD?

Research has shown that finerenone has been studied for heart failure and has demonstrated promising safety results. In one study, finerenone's safety matched that of a placebo, indicating it did not cause more side effects than a fake treatment. Another study found that finerenone reduced the risk of worsening heart failure and heart-related deaths.

While these results are positive, studies also track any health issues in participants. Researchers frequently check blood pressure, heart rate, and kidney function to ensure the treatment remains safe.

In this ongoing research, special attention focuses on monitoring potassium levels because finerenone can affect them. Monitoring is crucial to catch any issues early. Overall, studies so far suggest that finerenone is well-tolerated, but monitoring during the trial helps ensure participant safety.12345

Why do researchers think this study treatment might be promising for heart failure?

Finerenone is unique because it targets a specific receptor in the kidney known as the mineralocorticoid receptor, which plays a role in fluid and sodium retention linked to heart failure. Unlike traditional treatments like ACE inhibitors or beta-blockers, finerenone offers a novel approach by directly reducing inflammation and fibrosis in heart tissues. Researchers are excited about finerenone because it has the potential to improve heart function with fewer side effects related to potassium levels compared to older mineralocorticoid receptor antagonists.

What evidence suggests that finerenone might be an effective treatment for heart failure with LVSD?

Research has shown that finerenone can help treat heart failure. In studies, finerenone lowered the risk of death from heart problems and reduced hospital visits for heart failure. For instance, one study found fewer heart-related events in people taking finerenone compared to those who did not. Another study showed that finerenone decreased the number of hospital visits due to heart failure. This treatment works by blocking a protein that causes inflammation and damage in the heart, which may help the heart pump blood more effectively. These findings suggest that finerenone could be a promising option for managing heart failure with left ventricular systolic dysfunction. Participants in this trial will receive finerenone treatment in an open-label safety extension.12367

Are You a Good Fit for This Trial?

This trial is for children and young adults up to 18 years old with heart failure and left ventricular systolic dysfunction (LVSD). Participants must be either newly enrolled infants under 6 months or from the earlier FIORE study, continuing their standard heart failure treatment alongside finerenone.

Inclusion Criteria

For participants rolling over from randomized controlled trial (RCT): Prior participation in the finerenone Phase 3 study FIORE (21466) and not permanently discontinued from the study intervention prior to the end of treatment (EoT) visit in FIORE.
My baby's heart is not pumping well, with an ejection fraction of 50% or less.
My baby weighs at least 3 kg.
See 3 more

Exclusion Criteria

For participants rolling over from randomized controlled trial (RCT): To roll-over to FIORELLO, all participants: Potassium (K+) >5.5 mmol/L. After unblinding:
My potassium level is above 5.5 mmol/L after taking finerenone.
My kidney function is very low, with an eGFR under 30.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive finerenone treatment in addition to standard care for heart failure and LVSD

9 months
At least 6 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

1 month

Open-label extension

Participants continue to receive finerenone treatment to evaluate long-term safety

10-11 months

What Are the Treatments Tested in This Trial?

Interventions

  • Finerenone
Trial Overview The safety and effectiveness of long-term use of finerenone in treating LVSD are being tested. Finerenone aims to improve heart function by reducing inflammation and scarring. The trial includes regular monitoring through blood tests, physical exams, ECGs, echocardiography, and feedback on medication effects.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Finerenone Open-Label Safety ExtensionExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Bayer

Lead Sponsor

Trials
2,291
Recruited
25,560,000+
Founded
1863
Headquarters
Leverkusen, Germany
Known For
Pharmaceutical Innovations
Top Products
Aspirin, Aleve, Yaz, Nexavar

Bill Anderson

Bayer

Chief Executive Officer since 2023

BSc in Chemical Engineering from the University of Texas, MSc in Chemical Engineering and Management from MIT

Michael Devoy profile image

Michael Devoy

Bayer

Chief Medical Officer since 2014

MD, PhD

Citations

A Prespecified Analysis of the FINEARTS-HF TrialIn patients with HF with mildly reduced or preserved ejection fraction, finerenone reduced the risk of cardiovascular death and worsening HF events, ...
2.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/40505158/
Efficacy and Safety of Finerenone in Heart Failure With ...Over a median follow-up of 2.5 years, finerenone reduced cardiovascular death or heart failure hospitalization compared with placebo (HR: 0.87 ...
Efficacy and Tolerability of Finerenone According to the ...The incidence rate of the primary outcome in this group was 10.2 (95% CI, 7.6-13.9) per 100 person-years (eTable 2 and eFigure 2 in Supplement 3) ...
Finerenone in Heart Failure with Mildly Reduced or ...Over a median follow-up of 32 months, 1083 primary-outcome events occurred in 624 of 3003 patients in the finerenone group, and 1283 primary- ...
Finerenone in heart failure and chronic kidney disease with ...Finerenone further reduced the risk of hospitalization from heart failure (HR: 0.83; 95% CI: 0.75–0.92; P < 0.001) and the composite kidney ...
Finerenone According to Frailty in Heart FailureCompared with placebo, finerenone reduced the risk of worsening HF events and cardiovascular deaths and improved symptoms in patients with HFmrEF or HFpEF ...
Finerenone and New York Heart Association Functional ...NYHA functional class improved similarly in the finerenone and placebo arms out to 12 months. The safety profile of finerenone was similar among participants ...
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