Abstract 4359878: Effect of mavacamten treatment by duration of obstructive hypertrophic cardiomyopathy diagnosis: Results from the EXPLORER cohort of MAVA-Long-Term Extension study

A Anjali Owens A Artur Oreziak (National Institute of Cardiology, Warsaw, Poland) R Roberto Barriales-Villa (Complexo Hospitalario Universitario A Coruña, Instituto de Investigación Biomédica de A Coruña, CIBERCV–Instituto de Salud Carlos III, A Coruña, Spain) T Theodore Abraham (Department of Cardiology, University of, California, San Francisco, San Francisco) T Timothy Wong (University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States) D David Fermin (Corewell Health, Grand Rapids, Michigan, United States) L Lubna Choudhury (Northwestern University, Feinberg School of Medicine, Chicago, Illinois, United States) P Philippe Charron (Sorbonne Université, AP-HP, IHU-ICAN, INSERM 1166, Hôpital Universitaire Pitié-Salpêtrière, Paris, France) T Tim Seidler J John Stendahl (Yale School of Medicine, New Haven, Connecticut, United States) G Ganesh Balaratnam (Bristol Myers Squibb, Princeton, New Jersey, United States) N Nadisha Weerackoon (Bristol Myers Squibb, Princeton, New Jersey, United States) B Bharat Suryawanshi (Bristol Myers Squibb, Princeton, New Jersey, United States) S Sheila Hegde (The University of Texas Southwestern Medical Center, Dallas, Texas, United States) I Iacopo Olivotto (Department of Cardiology, Meyer Children’s Hospital, IRCCS, Florence, Italy)

Abstract

Introduction: Interim analyses from MAVA-LTE (NCT03723655) demonstrated that mavacamten is efficacious and well tolerated in patients with obstructive hypertrophic cardiomyopathy (oHCM). The relationship between the duration of oHCM diagnosis at mavacamten initiation and the effects of mavacamten are unknown. Research Questions: To assess the effects of mavacamten in patients from the EXPLORER cohort of MAVA-LTE by duration of oHCM diagnosis. Methods: All patients in MAVA-LTE received mavacamten. The effects of mavacamten on echocardiographic parameters and disease biomarker levels by duration of oHCM diagnosis were assessed (data cut-off: April 5, 2024). Results: In total, 231 patients were categorized into 4 subgroups based on duration of oHCM diagnosis at mavacamten initiation: 0–2.5 years (n=61), 2.5–5 years (n=49), 5–10 years (n=64) and >10 years (n=57) ( Table 1 ). At MAVA-LTE baseline, patients in the 0–2.5 years group had lower resting and Valsalva left ventricular outflow tract (LVOT) gradients, left atrial volume index (LAVI), interventricular septum (IVS) thickness, ratio of early diastolic mitral inflow velocity to mitral annular velocity (E/e’), and N-terminal pro B-type natriuretic peptide (NT-proBNP) levels than patients in other subgroups, while a higher proportion were New York Heart Association Class I ( Table 1 and 2 ). By week 204, improvements in LAVI ( Figure 1 ) were observed in all groups with abnormal baseline values ( Table 2 ). For resting and Valsalva LVOT gradients, E/e’, LVMI, and NT-proBNP levels, values improved from baseline in all subgroups by week 204 ( Table 2 ). IVS thickness improved from baseline in all subgroups by week 204 but remained elevated. Exposure adjusted incidence rates for serious treatment emergent adverse events per 100 patient-years of exposure were generally similar across subgroups (0–2.5 yrs: 9.30; 2.5–5 yrs: 7.04; 5–10 yrs: 12.33; >10 yrs: 11.53). Conclusion: Patients in MAVA-LTE who had a shorter duration from diagnosis of oHCM to mavacamten initiation had lower values for key echocardiographic parameters and disease biomarker levels at baseline than those with a longer duration. Mavacamten treatment trended towards improvement in echocardiographic parameters and disease biomarker levels regardless of the duration of oHCM diagnosis.

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)

A

Anjali Owens

A

Artur Oreziak

National Institute of Cardiology, Warsaw, Poland

R

Roberto Barriales-Villa

Complexo Hospitalario Universitario A Coruña, Instituto de Investigación Biomédica de A Coruña, CIBERCV–Instituto de Salud Carlos III, A Coruña, Spain

T

Theodore Abraham

Department of Cardiology, University of, California, San Francisco, San Francisco

T

Timothy Wong

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

D

David Fermin

Corewell Health, Grand Rapids, Michigan, United States

L

Lubna Choudhury

Northwestern University, Feinberg School of Medicine, Chicago, Illinois, United States

P

Philippe Charron

Sorbonne Université, AP-HP, IHU-ICAN, INSERM 1166, Hôpital Universitaire Pitié-Salpêtrière, Paris, France

T

Tim Seidler

J

John Stendahl

Yale School of Medicine, New Haven, Connecticut, United States

G

Ganesh Balaratnam

Bristol Myers Squibb, Princeton, New Jersey, United States

N

Nadisha Weerackoon

Bristol Myers Squibb, Princeton, New Jersey, United States

B

Bharat Suryawanshi

Bristol Myers Squibb, Princeton, New Jersey, United States

S

Sheila Hegde

The University of Texas Southwestern Medical Center, Dallas, Texas, United States

I

Iacopo Olivotto

Department of Cardiology, Meyer Children’s Hospital, IRCCS, Florence, Italy