Universitaetsklinik Heidelberg
Heidelberg, 69120, Germany
Location status: Recruiting
NCT Number: NCT07235462
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.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Heidelberg, 69120, Germany
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Follow clinical practice/administration.
Other names: BEYONTTRA
Time frame: Baseline (Initial study visit)
Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.
Time frame: Baseline (Initial study visit)
Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.
Time frame: Baseline (Initial study visit)
Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.
Time frame: Baseline (Initial study visit)
Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.
Time frame: Baseline (Initial study visit)
Demographic characteristics at the first documented regular visit in the study, referred to as the initial study visit.
Time frame: Baseline up to 15 months
ATTR-CM type: mixed phenotype (yes/no)
Time frame: Baseline up to 15 months
ATTR-CM type: genetic status (mutation / wild type; if mutation: genotype and zygosity)
Time frame: Baseline up to 15 months
ATTR-CM diagnosis (year of diagnosis)
Time frame: Baseline up to 15 months
ATTR-CM setting of diagnosis: (endomyocardial biopsy
/ non-invasive / both, NYHA classification at diagnosis)
Time frame: Baseline up to 15 months
ATTR-CM manifestations (type)
Time frame: Baseline up to 15 months
ATTR-CM-relevant comorbidities (type)
Time frame: Baseline up to 15 months
Prior and concomitant ATTR-CM-relevant procedures (type)
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)
Time frame: Baseline up to 15 months
Concomitant medications administered alongside acoramidis (name)
Time frame: Baseline up to 15 months
Acoramidis initiation (date)
Time frame: Baseline up to 15 months
Acoramidis initiation (if patient is switching from a different therapy: reason for switch)
Time frame: Baseline up to 15 months
Acoramidis discontinuation (reason)
Time frame: Baseline up to 15 months
Acoramidis interruption (reason)
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)
Time frame: From acoramidis initiation up to end of observation (approximately 12-15 months).
Adverse events (AEs) documentation
Time frame: From acoramidis initiation up to end of observation (approximately 12-15 months).
Serious Adverse events (SAEs) documentation
Contact information is provided by the study sponsor or research team.
Bayer
Industry
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
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.
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