TY - JOUR
T1 - Safety and Efficacy of Metabolic Modulation With Ninerafaxstat in Patients With Nonobstructive Hypertrophic Cardiomyopathy
AU - Maron, Martin S.
AU - Mahmod, Masliza
AU - Abd Samat, Azlan Helmy
AU - Choudhury, Lubna
AU - Massera, Daniele
AU - Phelan, Dermot M.J.
AU - Cresci, Sharon
AU - Martinez, Matthew W.
AU - Masri, Ahmad
AU - Abraham, Theodore P.
AU - Adler, Eric
AU - Wever-Pinzon, Omar
AU - Nagueh, Sherif F.
AU - Lewis, Gregory D.
AU - Chamberlin, Paul
AU - Patel, Jai
AU - Yavari, Arash
AU - Dehbi, Hakim Moulay
AU - Sarwar, Rizwan
AU - Raman, Betty
AU - Valkovič, Ladislav
AU - Neubauer, Stefan
AU - Udelson, James E.
AU - Watkins, Hugh
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/5/28
Y1 - 2024/5/28
N2 - Background: In nonobstructive hypertrophic cardiomyopathy (nHCM), there are no approved medical therapies. Impaired myocardial energetics is a potential cause of symptoms and exercise limitation. Ninerafaxstat, a novel cardiac mitotrope, enhances cardiac energetics. Objectives: This study sought to evaluate the safety and efficacy of ninerafaxstat in nHCM. Methods: Patients with hypertrophic cardiomyopathy and left ventricular outflow tract gradient <30 mm Hg, ejection fraction ≥50%, and peak oxygen consumption <80% predicted were randomized to ninerafaxstat 200 mg twice daily or placebo (1:1) for 12 weeks. The primary endpoint was safety and tolerability, with efficacy outcomes also assessed as secondary endpoints. Results: A total of 67 patients with nHCM were enrolled at 12 centers (57 ± 11.8 years of age; 55% women). Serious adverse events occurred in 11.8% (n = 4 of 34) in the ninerafaxstat group and 6.1% (n = 2 of 33) of patients in the placebo group. From baseline to 12 weeks, ninerafaxstat was associated with significantly better VE/VCO2 (ventilatory efficiency) slope compared with placebo with a least-squares (LS) mean difference between the groups of −2.1 (95% CI: −3.6 to −0.6; P = 0.006), with no significant difference in peak VO2 (P = 0.90). The Kansas City Cardiomyopathy Questionnaire Clinical Summary Score was directionally, though not significantly, improved with ninerafaxstat vs placebo (LS mean 3.2; 95% CI: −2.9 to 9.2; P = 0.30); however, it was statistically significant when analyzed post hoc in the 35 patients with baseline Kansas City Cardiomyopathy Questionnaire Clinical Summary Score ≤80 (LS mean 9.4; 95% CI: 0.3-18.5; P = 0.04). Conclusions: In symptomatic nHCM, novel drug therapy targeting myocardial energetics was safe and well tolerated and associated with better exercise performance and health status among those most symptomatically limited. The findings support assessing ninerafaxstat in a phase 3 study.
AB - Background: In nonobstructive hypertrophic cardiomyopathy (nHCM), there are no approved medical therapies. Impaired myocardial energetics is a potential cause of symptoms and exercise limitation. Ninerafaxstat, a novel cardiac mitotrope, enhances cardiac energetics. Objectives: This study sought to evaluate the safety and efficacy of ninerafaxstat in nHCM. Methods: Patients with hypertrophic cardiomyopathy and left ventricular outflow tract gradient <30 mm Hg, ejection fraction ≥50%, and peak oxygen consumption <80% predicted were randomized to ninerafaxstat 200 mg twice daily or placebo (1:1) for 12 weeks. The primary endpoint was safety and tolerability, with efficacy outcomes also assessed as secondary endpoints. Results: A total of 67 patients with nHCM were enrolled at 12 centers (57 ± 11.8 years of age; 55% women). Serious adverse events occurred in 11.8% (n = 4 of 34) in the ninerafaxstat group and 6.1% (n = 2 of 33) of patients in the placebo group. From baseline to 12 weeks, ninerafaxstat was associated with significantly better VE/VCO2 (ventilatory efficiency) slope compared with placebo with a least-squares (LS) mean difference between the groups of −2.1 (95% CI: −3.6 to −0.6; P = 0.006), with no significant difference in peak VO2 (P = 0.90). The Kansas City Cardiomyopathy Questionnaire Clinical Summary Score was directionally, though not significantly, improved with ninerafaxstat vs placebo (LS mean 3.2; 95% CI: −2.9 to 9.2; P = 0.30); however, it was statistically significant when analyzed post hoc in the 35 patients with baseline Kansas City Cardiomyopathy Questionnaire Clinical Summary Score ≤80 (LS mean 9.4; 95% CI: 0.3-18.5; P = 0.04). Conclusions: In symptomatic nHCM, novel drug therapy targeting myocardial energetics was safe and well tolerated and associated with better exercise performance and health status among those most symptomatically limited. The findings support assessing ninerafaxstat in a phase 3 study.
KW - cardiac energetics
KW - clinical trial
KW - exercise capacity
KW - health status
KW - ninerafaxstat
KW - nonobstructive hypertrophic cardiomyopathy
UR - http://www.scopus.com/inward/record.url?scp=85191063395&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2024.03.387
DO - 10.1016/j.jacc.2024.03.387
M3 - Article
C2 - 38599256
AN - SCOPUS:85191063395
SN - 0735-1097
VL - 83
SP - 2037
EP - 2048
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 21
ER -