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临床试验/CTRI/2023/10/058870
CTRI/2023/10/058870招募中3 期

A Randomized Double-blind Placebo-controlled Clinical Study to Evaluate Mavacamten in Adults with Symptomatic Non-obstructive Hypertrophic Cardiomyopathy - ODYSSEY study

MyoKardia, Inc.0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1) Diagnosis of HCM consistent with current American College of Cardiology Foundation/American Heart Association and European Society of Cardiology guidelines: unexplained left-ventricular hypertrophy with non-dilated ventricular chambers in the absence of other cardiac or systemic disease which can produce the required magnitude of hypertrophy of a maximal LV wall thickness greater than or equal to 15 mm. 2) Peak LVOT pressure gradient < 30 mm Hg at rest and < 50 mm Hg with provocation. 3) New York Heart Association (NYHA) Class II or III. 4) KCCQ-23 CSS Score less than or equal to 80 at screening. 5) LVEF greater than or equal to 60%. 6) CPET: Documented oxygen saturation at rest > 90% at screening. 7) NT-proBNP greater than or equal to 200 pg/mL or BNP greater than or equal to 70 pg/mL. 8) Evidence of myocardial damage or Evidence of LV diastolic dysfunction.

排除标准

  • 1) Known infiltrative or storage disorder causing cardiac hypertrophy that mimics nHCM. 2) History of unexplained syncope within 6 months prior to screening. 3) History of sustained ventricular tachyarrhythmia ( > 30 seconds) within 6 months prior to screening. 4) Paroxysmal or persistent (non-permanent) AF detected at the time of screening. 5) ICD placement or pulse generator change within 2 months prior to screening or planned new ICD placement during the study. 6) Acute heart failure from 4 weeks prior to screening up to randomization. 7) Coronary artery disease requiring intervention. 8) Heart transplant recipient or listed for heart transplant. 9) Currently implanted LV assist device. 10) Clinically significant pulmonary disease associated with exertional dyspnea. 11) Any documented active or suspected malignancy or history of malignancy within 2 years prior to screening. 12) Clinically documented LV aneurysm greater than or equal to 2 cm

研究者

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