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Cardiac Magnetic Resonance and Echocardiography Study With Acoramidis

RECRUITINGPhase 4Sponsored by Eidos Therapeutics, a BridgeBio company
Actively Recruiting
PhasePhase 4
SponsorEidos Therapeutics, a BridgeBio company
Started2026-07
Est. completion2030-08
Eligibility
Age18 Years – 80 Years
Healthy vol.Accepted
Locations1 site

Summary

The study aims to evaluate the effect of acoramidis on cardiac functional and structural improvement in participants with ATTR-CM.

Eligibility

Age: 18 Years – 80 YearsHealthy volunteers accepted
Key Inclusion Criteria:

* Participants aged 18 to 80
* Confirmed diagnosis of ATTR-CM requiring targeted therapy
* At screening: New York Heart Association (NYHA) Class I/II; estimated glomerular filtration rate (eGFR) ≥40 mL/min/1.73m2; left ventricular ejection fraction (LVEF) \>35%; left ventricular (LV) wall thickness ≥12 mm.
* Heart failure condition has been clinically stable for at least 6 weeks prior to screening.

Key Exclusion Criteria:

* Current or planned implantation of a cardiac implantable electronic device (eg, pacemaker, implantable cardiac defibrillator).
* Acute myocardial infarction, acute coronary syndrome or coronary revascularization, or experienced stroke or transient ischemic attack within 90 days prior to screening.
* Hemodynamic instability.
* Likely to undergo heart transplantation within 12 months from screening.
* Confirmed diagnosis of AL amyloidosis at screening.
* At screening: NYHA Class III/IV; National Amyloidosis Center (NAC) Stage 3.
* Prior or current treatment with acoramidis.

Conditions6

Alzheimer's DiseaseAmyloid CardiomyopathyAmyloidosisHeart DiseaseTransthyretin AmyloidosisTransthyretin Amyloidosis Cardiomyopathy (ATTR-CM)

Interventions1

Locations1 site

Washington University in St. Louis
St Louis, Missouri, 63110

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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