Abstract 4370461: Aficamten is safe and effective in oHCM with comorbidities obesity, hypertension, and diabetes: a SEQUOIA-HCM sub-study

M Matthew Lee T Theodore Abraham (Department of Cardiology, University of, California, San Francisco, San Francisco) B Brian Claggett (Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School, Boston) M Martin maron (Lahey Hospital, Burlington, Massachusetts, United States) Z Zi Miao (Brigham and Women's Hospital, Boston, Massachusetts, United States) B Benjamin Meder (Precision Digital Health, Department of Internal Medicine III, Cardiology, University Heidelberg, Heidelberg, Germany) I Iacopo Olivotto (Department of Cardiology, Meyer Children’s Hospital, IRCCS, Florence, Italy) S Stephen Heitner (Cytokinetics Inc., South San Francisco, California, United States) D Daniel Jacoby (Cytokinetics Inc., South San Francisco, California, United States) F Fady Malik (Cytokinetics Inc., South San Francisco, California, United States) S Stuart Kupfer (Cytokinetics, South San Francisco, CA) A Amy Wohltman (Cytokinetics, South San Francisco, CA) C Caroline Coats (University og Glasgow, Glasgow, United Kingdom)

Abstract

Introduction/Background: Obesity, hypertension, and diabetes commonly coexist with obstructive hypertrophic cardiomyopathy (oHCM), potentially influencing symptom burden and functional limitation. It is not known if aficamten provides similar benefit across comorbidity subgroups. Research Questions/Hypothesis: Efficacy of aficamten in patients with oHCM and comorbidities. Methods/Approach: SEQUOIA-HCM (NCT05186818) randomized 282 adults with symptomatic oHCM to aficamten or placebo for 24 weeks. Participants were grouped by obesity (body mass index [BMI] ≥30 kg/m 2 ), hypertension (history or average screening/baseline systolic blood pressure ≥140 or diastolic blood pressure ≥90 mmHg), and diabetes (type 1, type 2, or unspecified per history). Baseline characteristics and treatment effects on peak oxygen uptake (pVO 2 ) and secondary endpoints were compared across comorbidity groups. Results/Data: At baseline, 32% had obesity, 55% had hypertension, and 8% had diabetes; 24% had 2 comorbidities, and 3% had all 3 comorbidities. At baseline, obesity was associated with lower Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (KCCQ-CSS), N-terminal pro-B-type natriuretic peptide (NT-proBNP), pVO 2 , and resting left ventricular outflow tract gradient (LVOT-G), and higher use of beta-blockers and disopyramide ( Table 1 ). At baseline, hypertension was associated with lower NT-proBNP, pVO 2 , and resting LVOT-G; older age; more atrial fibrillation and diabetes; and more use of non-dihydropyridine calcium-channel blockers and renin angiotensin system blockers. At baseline, diabetes was associated with older age, hypertension, higher KCCQ-CSS, lower NT-proBNP, and pVO 2 , and more use of renin angiotensin system blockers. Despite baseline differences, aficamten treatment compared to placebo consistently improved pVO 2 , KCCQ-CSS, Valsalva LVOT-G, and NT-proBNP independent of comorbid status (all interaction p-values >0.05) ( Figure 1; Table 2 ). The incidence of serious adverse events and left ventricular ejection fraction <50% were similar across subgroups, including when grouped by treatment arm. Conclusion(s): Comorbidities, particularly obesity and hypertension, are common in patients with oHCM. Aficamten treatment showed consistent clinical efficacy regardless of comorbidity status, supporting its use across a broad patient population.

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 (13)

M

Matthew Lee

T

Theodore Abraham

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

B

Brian Claggett

Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School, Boston

M

Martin maron

Lahey Hospital, Burlington, Massachusetts, United States

Z

Zi Miao

Brigham and Women's Hospital, Boston, Massachusetts, United States

B

Benjamin Meder

Precision Digital Health, Department of Internal Medicine III, Cardiology, University Heidelberg, Heidelberg, Germany

I

Iacopo Olivotto

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

S

Stephen Heitner

Cytokinetics Inc., South San Francisco, California, United States

D

Daniel Jacoby

Cytokinetics Inc., South San Francisco, California, United States

F

Fady Malik

Cytokinetics Inc., South San Francisco, California, United States

S

Stuart Kupfer

Cytokinetics, South San Francisco, CA

A

Amy Wohltman

Cytokinetics, South San Francisco, CA

C

Caroline Coats

University og Glasgow, Glasgow, United Kingdom