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Taking people4. fázis

Cardiac Magnetic Resonance and Echocardiography Study With Acoramidis

Key facts

Where
Aarhus N, DániaSee the site
Phase
4. fázis

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Forrás: NCT07695701: ki vehet részt

Where in Dánia

  • Region MidtjyllandAarhus N, DániaToborzás még nem indult

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Eidos Therapeutics, a BridgeBio company
Trial code
NCT07695701EU 2026-526068-19-00
Record updated
2026. július 29.
Original description
The study aims to evaluate the effect of acoramidis on cardiac functional and structural improvement in participants with ATTR-CM.Read full original descriptionShow less

An Open-Label Study to Investigate the Long-Term Effects of Acoramidis on Cardiac Function, Structure and Cardiac Amyloid Burden in Participants With Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

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

Inclusion: 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.

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

ClinicalTrials.gov NCT07695701 · EU CTIS 2026-526068-19-00