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Impact of Agalsidase Alfa Therapy on Cardiac funcTION in Patients With Fabry's Cardiomyopathy

Impact of Agalsidase Alfa Therapy on Cardiac funcTION in Patients With Fabry's Cardiomyopathy (ACTION-Fabry Trial)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03230591
Enrollment
25
Registered
2017-07-26
Start date
2017-07-12
Completion date
2025-01-31
Last updated
2021-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fabry Disease

Keywords

Fabry's disease, Agalsidase Alfa, Cardiomyopathy, Enzyme replacement therapy, Diastolic stress echocardiography, LV vortex flow, Cardiac MRI

Brief summary

Study Design: This is an observational study. No treatment or intervention will be assigned to the subjects. All patients will receive full standard of care concomitant medication for the treatment of their cardiac condition. 25 patients with genetically confirmed Anderson-Fabry disease who have a plan to start ERT with Agalsidase Alfa will undergo 2D strain, diastolic stress echocardiography, LV vortex flow analysis, and CMR at baseline and after 1 year of treatment with ERT with Agalsidase Alfa for follow-up.

Detailed description

1. Objectives - The purpose of this study is to evaluate the impact of ERT with Agalsidase Alfa on LV diastolic function and flow in patients with Fabry's cardiomyopathy using LV 2D strain, diastolic stress echocardiography, LV vortex flow and CMR. 2. Primary / Secondary Endpoint 1) Primary endpoint: * Change from baseline in peak exercise E/E' by diastolic stress echocardiography, global longitudinal strain and LV vortex flow parameters at 1 year 2) Secondary endpoints: * Changes from baseline in extracellular volume by CMR (T1 mapping) at 1 year follow up * Changes from baseline in evaluation of the degree of the resting LV diastolic function * Changes from baseline in other echo-parameters; LV mass index, reduction of peak exercise E/E prime at 1 year follow up * Changes from baseline in quality of life using questionnaire ⑤ Change from baseline in peak VO2, exercise time, AT by diastolic stress echocardiography at 1 year follow up ⑥ Change in T1 baseline (myo, ms) & T1 baseline (blood, ms), T1 postcontrast (myo, ms) & T1 baseline (blood, ms) by CMR 3. Study Methods 1) Study Design: This is an observational study. No treatment or intervention will be assigned to the subjects. All patients will receive full standard of care concomitant medication for the treatment of their cardiac condition. 25 patients with genetically confirmed Anderson-Fabry disease who have a plan to start ERT with Agalsidase Alfa will undergo 2D strain, diastolic stress echocardiography, LV vortex flow analysis, and CMR at baseline and after 1 year of treatment with ERT with Agalsidase Alfa for follow-up.

Interventions

OTHEREchocardiography

LV vortex flow in Echocardiography

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 16\ 75 years with Fabry disease confirmed by enzyme assay and gene test * Patients who have LVH in 2D echocardiography (end diastolic septum and posterior wall thickness ≥ 12mm) or Patients who present with cardiac changes (indicative of disease progression such as decreased global longitudinal strain on 2D strain echocardiography or low native T1 mapping on CMR) * Patients provided written informed consent to participate in this study

Exclusion criteria

* Contraindication for enzyme replacement treatment with Agalsidase Alfa * Patients who cannot receive supine bicycle stress echocardiography, contrast echocardiography or CMR * Patients with hemodynamically significant valvular heart disease or arrhythmias * Patients who have history of acute myocardial infarction or congestive heart failure with reduced LV ejection fraction of less than 35% * Patients who had any cerebrovascular accident in the prior 6 months * Scheduled or planned surgery in the next 6 months * Patients with chronic liver cirrhosis * Patients who are allergic to contrast agent (e.g. Definity�, Lantheus Medical Imaging, North Billerica, MA, USA)

Design outcomes

Primary

MeasureTime frameDescription
peak exercise E/E' by diastolic stress echocardiography1 yearChange from baseline in peak exercise E/E' by diastolic stress echocardiography
global longitudinal strain1 year

Secondary

MeasureTime frameDescription
extracellular volume by CMR1 yearChanges from baseline in extracellular volume by CMR (T1 mapping) at 1 year follow up
evaluation of the degree of the resting LV diastolic function1 yearChanges from baseline in evaluation of the degree of the resting LV diastolic function
quality of life using questionnaire1 yearChanges from baseline in quality of life using questionnaire

Countries

South Korea

Contacts

Primary ContactGeu-Ru Hong, MD, Ph.D
grhong@yuhs.ac82-2-2228-8443

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026