Abstract 4365761: Acoramidis Lowers NT-proBNP in a Larger Proportion of ATTRibute-CM Study Participants With Transthyretin Amyloid Cardiomyopathy Compared with Placebo, Independent of Atrial Fibrillation Status

M Mathew Maurer (Columbia University, New York, New York, United States) K Kevin Alexander (Division of Cardiovascular Medicine, Department of Medicine, Stanford Center for Clinical Research, Stanford University School of Medicine, Palo Alto, California, United States) L Laura Obici (Fondazione IRCCS Policlinico San Matteo, Pavia, Italy) S Steen Poulsen (Aarhus University Hospital, Aarhus, Denmark) J James Januzzi (Baim Institute for Clinical Research, Boston, Massachusetts, United States) R Ronald Witteles (Stanford University, Stanford, California, United States) W Wael Jaber (Cleveland Clinic Coordinating Center for Clinical Research, Heart Vascular Thoracic Institute, Cleveland Clinic, Cleveland) Y Yevgeniy Brailovsky (Columbia University Irving Medical Center, New York, New York, United States) K Kai Vogtlaender (Bayer AG, Wuppertal, Germany) A Adam Castano (BridgeBio Pharma, Inc., San Francisco, California, United States) J Jean-Francois Tamby (BridgeBio Pharma, Inc., San Francisco, California, United States) J Jonathan Fox (BridgeBio Pharma, Inc., San Francisco, California, United States) S Sumeet Mitter (Inova Schar Heart and Vascular, Falls Church, Virginia, United States) M Mazen Hanna (Department of Cardiovascular Medicine, Heart, Vascular & Thoracic Institute, Cleveland Clinic, OH.) B Brett Sperry (Saint Luke’s Mid America Heart Institute and the University of Missouri-Kansas City, Kansas City, Missouri, United States)

Abstract

Background: Atrial fibrillation/flutter (AF/AFL) is a frequent complication of heart failure in transthyretin amyloid cardiomyopathy (ATTR-CM) and its increasing incidence is a marker of disease progression. Increasing N-terminal B-type natriuretic peptide (NT-proBNP) levels are also an independent indicator of ATTR-CM progression and higher NT-proBNP levels are seen in ATTR-CM with superimposed AF. Acoramidis achieves near-complete (≥90%) TTR stabilization, and is approved in the USA, UK, Europe and Japan for the treatment of ATTR-CM in adults. Acoramidis blunts the progressive rise in NT-proBNP, compared with placebo in patients with ATTR-CM. Research Question: How does acoramidis treatment influence ATTR-CM disease progression based on NT-proBNP levels in the presence or absence of AF/AFL? Methods: The ATTRibute-CM (NCT03860935) study has been published. This post hoc analysis was conducted in the modified intention-to-treat population who had baseline (BL) and Month 30 NT-proBNP assessments (n=413). Categories defined were: 1) presence or absence of AF/AFL diagnosis at BL (defined as recorded AF medical history or presence of AF/AFL on ECG at enrollment), 2) incidence of AF/AFL treatment-emergent adverse event (TEAE) during the study, and 3) AF/AFL at any time (defined as [1] or [2]). Clinically meaningful improvement at Month 30 was defined as a reduction of >300 pg/mL and >30% in NT-proBNP from BL. AF/AFL TEAEs were identified using ‘atrial fibrillation’, ‘atrial flutter’ and ‘cardiac flutter’ MedDRA preferred terms. Results: At study entry, participants with BL AF/AFL had lower 6-minute walk distances, left ventricular ejection fractions and Kansas City Cardiomyopathy Questionnaire Overall Summary scores, higher NT-proBNP levels and were more frequently categorized in higher National Amyloidosis Centre stages versus those without BL AF/AFL. Other BL characteristics were comparable between groups. At Month 30, a higher proportion of participants had improved NT-proBNP with acoramidis than with placebo, regardless of AF/AFL status at BL and/or development of AF/AFL during the study ( Table ). Conclusions: In ATTRibute-CM, the proportion of participants with improved NT-proBNP at Month 30 was consistently around 15 percentage points higher with acoramidis than placebo, regardless of AF/AFL status at BL or during the study. The ongoing open-label extension study may offer insights into the durability of this effect and its long-term clinical consequences.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (15)

M

Mathew Maurer

Columbia University, New York, New York, United States

K

Kevin Alexander

Division of Cardiovascular Medicine, Department of Medicine, Stanford Center for Clinical Research, Stanford University School of Medicine, Palo Alto, California, United States

L

Laura Obici

Fondazione IRCCS Policlinico San Matteo, Pavia, Italy

S

Steen Poulsen

Aarhus University Hospital, Aarhus, Denmark

J

James Januzzi

Baim Institute for Clinical Research, Boston, Massachusetts, United States

R

Ronald Witteles

Stanford University, Stanford, California, United States

W

Wael Jaber

Cleveland Clinic Coordinating Center for Clinical Research, Heart Vascular Thoracic Institute, Cleveland Clinic, Cleveland

Y

Yevgeniy Brailovsky

Columbia University Irving Medical Center, New York, New York, United States

K

Kai Vogtlaender

Bayer AG, Wuppertal, Germany

A

Adam Castano

BridgeBio Pharma, Inc., San Francisco, California, United States

J

Jean-Francois Tamby

BridgeBio Pharma, Inc., San Francisco, California, United States

J

Jonathan Fox

BridgeBio Pharma, Inc., San Francisco, California, United States

S

Sumeet Mitter

Inova Schar Heart and Vascular, Falls Church, Virginia, United States

M

Mazen Hanna

Department of Cardiovascular Medicine, Heart, Vascular & Thoracic Institute, Cleveland Clinic, OH.

B

Brett Sperry

Saint Luke’s Mid America Heart Institute and the University of Missouri-Kansas City, Kansas City, Missouri, United States