Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07235462

A Study to Learn About the Use of Acoramidis in Patients With a Heart Condition Called Transthyretin Amyloid Cardiomyopathy (ATTR-CM) in a Real-world Setting

Transthyretin Amyloid Cardiomyopathy (ATTR-CM) is a serious and life-threatening condition where a protein called transthyretin (TTR) misfolds and builds up as amyloid fibrils in the heart muscle. This buildup causes the heart to become stiff, leading to restrictive cardiomyopathy and progressive heart failure. There are two forms of ATTR-CM: a hereditary or 'variant' form (vATTR-CM) caused by a gene mutation, and a 'wild-type' form (wtATTR-CM) which is associated with aging. Because its symptoms can be similar to other heart conditions, ATTR-CM is often diagnosed late. However, recent advances in medical imaging are helping doctors to identify the disease earlier. Acoramidis is a new medication designed to treat ATTR-CM. It works by stabilizing the TTR protein, preventing it from misfolding and forming the harmful amyloid deposits. Acoramidis has been shown to be effective and safe in a major clinical trial (the ATTRibute-CM study), which led to its approval for use in both the United States and Europe. While clinical trials provide valuable information, data on how a new medicine performs in everyday clinical practice is also very important. This type of information is called real-world evidence. Currently, there is limited real-world information about the use of acoramidis. This study, called ACO-REAL, is an observational study, which means researchers will observe patients who are receiving acoramidis as part of their normal clinical care, without introducing any experimental interventions. The study will take place in approximately 20 European countries and aims to enroll up to 2,000 adults who have been diagnosed with either wild-type or variant ATTR-CM and are starting treatment with acoramidis. This includes patients who have not been treated for ATTR-CM before, as well as those who have been treated with other therapies. The main goals of the study are to understand the characteristics of patients being treated with acoramidis and to document how the treatment is used in routine medical practice. The study will also collect information on the safety of acoramidis. Furthermore, researchers will assess how the treatment affects patients' heart function, their functional capacity (such as their ability to walk), their overall health status, and their quality of life. The study will also track how often patients need to use healthcare resources like hospitals or emergency rooms. This information will help to improve the understanding and management of ATTR-CM in a real-world setting, ultimately aiming to optimize care for patients with this progressive disease.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Universitaetsklinik Heidelberg

Heidelberg, 69120, Germany

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • - Adults (≥18 years at the date of signing the informed consent form (ICF)).
  • Diagnosis of either wild-type or variant ATTR-CM.
  • Signed ICF.
  • Decision to initiate treatment with acoramidis was made as per treating investigator's routine treatment practice before signature of ICF.
  • Treatment start with acoramidis within 90 days after signing the ICF, with the possibility of starting acoramidis on the same day as signing the ICF.

Exclusion criteria

  • Participation in an investigational trial with interventions outside of routine clinical practice, except for participation in potential sub-studies related to this observational study. Please note: In addition to this observational study, separate sub-studies may be conducted to collect additional data. Participation in these sub-studies is voluntary and will be governed by separate protocols and informed consent processes. The main observational study does not include interventional procedures beyond routine clinical practice.
  • Contra-indications according to the local SmPC of acoramidis.
  • Patients who are unable to provide consent, including those whose consent would need to be given by a legal representative.

Treatment and study plan

Acoramidis (356 mg film-coated tablets)

Drug

Follow clinical practice/administration.

Other names: BEYONTTRA

Primary outcomes

  1. Patient demographic characteristics: age

    Time frame: Baseline (Initial study visit)

    Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.

  2. Patient demographic characteristics: sex

    Time frame: Baseline (Initial study visit)

    Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.

  3. Patient demographic characteristics: race

    Time frame: Baseline (Initial study visit)

    Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.

  4. Patient demographic characteristics: height

    Time frame: Baseline (Initial study visit)

    Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.

  5. Patient demographic characteristics: weight

    Time frame: Baseline (Initial study visit)

    Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.

  6. Clinical Characteristics: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Type

    Time frame: Baseline up to 15 months

    ATTR-CM type: mixed phenotype (yes/no)

  7. Clinical Characteristics: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Genetic status

    Time frame: Baseline up to 15 months

    ATTR-CM type: genetic status (mutation / wild type; if mutation: genotype and zygosity)

  8. Clinical Characteristics: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Diagnosis

    Time frame: Baseline up to 15 months

    ATTR-CM diagnosis (year of diagnosis)

  9. Clinical Characteristics: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Setting of Diagnosis

    Time frame: Baseline up to 15 months

    ATTR-CM setting of diagnosis: (endomyocardial biopsy

    / non-invasive / both, NYHA classification at diagnosis)

  10. Clinical Characteristics: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Manifestations

    Time frame: Baseline up to 15 months

    ATTR-CM manifestations (type)

  11. Clinical Characteristics: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) -relevant comorbidities

    Time frame: Baseline up to 15 months

    ATTR-CM-relevant comorbidities (type)

  12. Clinical Characteristics: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) -relevant procedures

    Time frame: Baseline up to 15 months

    Prior and concomitant ATTR-CM-relevant procedures (type)

  13. Treatment Patterns with Acoramidis: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) -related medications

    Time frame: Baseline (assessment within the past 12 months prior to initiation)

    Previously administered ATTR-CM-related medications within the past 12 months before initial visit (name)

  14. Treatment Patterns with Acoramidis: Transthyretin Amyloid Cardiomyopathy (ATTR-CM) concomitant medications

    Time frame: Baseline up to 15 months

    Concomitant medications administered alongside acoramidis (name)

  15. Treatment Patterns with Acoramidis: Initiation

    Time frame: Baseline up to 15 months

    Acoramidis initiation (date)

  16. Treatment Patterns with Acoramidis: Initiation after a different therapy

    Time frame: Baseline up to 15 months

    Acoramidis initiation (if patient is switching from a different therapy: reason for switch)

  17. Treatment Patterns with Acoramidis: discontinuation

    Time frame: Baseline up to 15 months

    Acoramidis discontinuation (reason)

  18. Treatment Patterns with Acoramidis: interruption

    Time frame: Baseline up to 15 months

    Acoramidis interruption (reason)

  19. Treatment Patterns with Acoramidis: prescription / refills

    Time frame: Baseline up to 15 months

    Acoramidis prescriptions/refills since the last visit or telephone contact (duration of time from initiation to discontinuation of therapy)

Secondary outcomes

  1. Incidence of Adverse Events

    Time frame: From acoramidis initiation up to end of observation (approximately 12-15 months).

    Adverse events (AEs) documentation

  2. Incidence of Serious Adverse Events

    Time frame: From acoramidis initiation up to end of observation (approximately 12-15 months).

    Serious Adverse events (SAEs) documentation

Study contacts

Contact information is provided by the study sponsor or research team.

Bayer Clinical Trials Contact

CONTACT

[email protected]

(+)1-888-84 22937

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Official study title

ACO-REAL - A Non-interventional Study Providing Insights Into the Use of Acoramidis in Patients With ATTR Amyloidosis With Cardiomyopathy (ATTR-CM) in Routine Clinical Practice

Acronym: ACO-REAL

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Nov 19, 2025
Registry last updated
Jul 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.