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Clinical Trials in the EU / 2026-526068-19-00
Authorised Phase IV

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)

2026-526068-19-00 · tracked via the Priya Life Science EU tracker
Sponsor
Eidos Therapeutics Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Cardiovascular Diseases
Decision date
20/08/2026
Enrollment target
50
Sites
Spain, Denmark

Condition studied

Transthyretin Amyloidosis

Investigational medicinal product(s)

BEYONTTRA 356 mg film-coated tablets

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Response based on improved LVEF or LVSVi at Month 36, Incidence of treatment-emergent AEs, SAEs

Endpoint detail

1. Response based on improved or stabilized LVEF AND improved or stabilized LVSVi at Month 36., 2. Response based on stabilized LVEF AND stabilized LVSVi at Month 36., 3. LVEF, at Month 36: - Mean change from baseline in LVEF - Response based on improved LVEF -Response based on improved or stabilized LVEF - Response based on stabilized LVEF, 4. LVSVi, at Month 36: - Mean change from baseline in LVSVi - Response based on improved LVSVi - Response based on improved or stabilized LVSVi - Response based on stabilized LVSVi, 5. LVGLS, at Month 36: - Mean change from baseline in LVGLS - Response based on improved LVGLS - Response based on improved or stabilized LVGLS - Response based on stabilized LVGLS, 6. LVMi, at Month 36: - Mean change from baseline in LVMi - Response based on improved LVMi - Response based on improved or stabilized LVMi - Response based on stabilized LVMi, 7. ECV, at Month 36: - Mean change from baseline in ECV - Response based on improved ECV - Response based on improved or stabilized ECV - Response based on stabilized ECV

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-526068-19-00 on CTIS ↗ ← All trials in the EU