Why the study?
Mavacamten has demonstrated efficacy and safety internationally for symptomatic obstructive hypertrophic cardiomyopathy, but clinical evidence in the Chinese population is lacking.
Does mavacamten improve Valsalva LVOT peak gradient in Chinese adults with symptomatic obstructive hypertrophic cardiomyopathy?
Does mavacamten improve Valsalva LVOT peak gradient in Chinese adults with symptomatic obstructive hypertrophic cardiomyopathy?
The EXPLORER-CN trial will determine the efficacy and safety of mavacamten for reducing LVOT gradients in Chinese patients with symptomatic obstructive hypertrophic cardiomyopathy.
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Addresses evidence gap for mavacamten in Chinese obstructive HCM; extends prior global RCT data to this population.
INTRODUCTION: Hypertrophic cardiomyopathy (HCM) is a primary myocardial disease commonly caused by pathogenic genetic variants encoding sarcomere proteins. Mavacamten, a first-in-class allosteric inhibitor of cardiac-specific myosin, has demonstrated efficacy and safety in international clinical trials of patients with symptomatic obstructive HCM (oHCM) but clinical evidence for mavacamten in the Chinese population is lacking. METHODS AND ANALYSIS: EXPLORER-CN is a multicentre, phase III, randomised, double-blind, placebo-controlled registration trial to evaluate the efficacy and safety of mavacamten in Chinese adults with symptomatic oHCM. The study will enrol approximately 81 participants with symptomatic oHCM. Eligible participants are randomised 2:1 to receive once-daily, oral mavacamten (starting dose 2.5 mg/day), or matching placebo, for 30 weeks, followed by a long-term extension (LTE) period of 48 weeks with active treatment for all subjects. The mavacamten dose will be adjusted by pharmacokinetic (PK)/pharmacodynamic (PD) parameters during the double-blinded, placebo-controlled period and PD-only during the LTE period. The primary efficacy endpoint is change from baseline to week 30 in Valsalva left ventricular outflow tract (LVOT) peak gradient determined by Doppler echocardiography. Secondary efficacy endpoints are change in resting LVOT peak gradient, proportion of participants achieving a Valsalva LVOT peak gradient <30 or < 50 mm Hg, New York Heart Association functional class improvement, change in Kansas City Cardiomyopathy Questionnaire Clinical Summary Score, cardiac biomarkers and left ventricular mass index evaluated by cardiac magnetic resonance. LTE endpoints will characterise the long-term safety and efficacy of mavacamten. ETHICS AND DISSEMINATION: This clinical study has been approved by the Drug Clinical Trial Ethics Committee of the Chinese Academy of Medical Sciences & Peking Union Medical College Hospital (reference number: HS2021089). Written informed consent will be obtained from each participant. The results will be published in peer-reviewed journals and presented during national and international conferences. TRIAL REGISTRATION NUMBER: NCT05174416.
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Tian et al. (2023) studied this question.
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