Current State of Hypertrophic Cardiomyopathy Clinical Trials

被引:13
|
作者
Khachfe, Hussein H. [1 ,2 ]
Salhab, Hamza A. [1 ,2 ]
Fares, Mohamad Y. [1 ,2 ]
Khachfe, Hassan M. [3 ]
机构
[1] Amer Univ Beirut, Fac Med, Beirut, Lebanon
[2] Lebanese Univ, Fac Med Sci, Neurosci Res Ctr, Beirut, Lebanon
[3] Lebanese Int Univ, Sch Arts & Sci, Lebanese Inst Biomed Res & Applicat, Beirut, Lebanon
关键词
SARCOMERE MUTATION CARRIERS; CLINICALTRIALS.GOV; DIAGNOSIS; LOSARTAN; ENERGY;
D O I
10.1016/j.gheart.2019.07.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Hypertrophic cardiomyopathy (HCM) is a genetic disorder with a very large global burden for which more therapeutic management regimens are required. Objectives. In this study, the authors explore HCM-related clinical trials, determine the shortcomings leading to the lack of development of new HCM therapies, and attempt to shed light on potential areas for improvement. Methods: In January 2019, the authors completed a search on ClinicalTrials.gov for all therapeutic and interventional clinical trials involving HCM, without any limits for location or date. Information on trial characteristics such as phase, start and end dates, sample size, experimental intervention, publications, study design, selection criteria, and results were collected and analyzed. Results: Sixty-three trials met the selection criteria. The average trial duration across phases was around 3 years. Around one-half of the trials were conducted in North America (United States and Canada) and 44% of the trials were in their early phases (I and II). Approximately one-third of the trials were completed. Only 14 publications were produced from all the clinical trials studied. Conclusions: The study revealed a low number of trials, lack of geographic diversity, and scarcity of published results concerning HCM clinical trials. Proper management of HCM trials is of vast importance to achieve effective therapies.
引用
收藏
页码:317 / 325
页数:9
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