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临床试验/jRCT2080220801
jRCT2080220801未知2 期

Early phase II clinical study with AT-877ER in patients with pulmonary arterial hypertension

ASAHI KASEI PHARMA CORPORATION0 个研究点开始时间: 待定
适应症

试验速览

阶段
2 期

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
干预模型
Double-blind

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • (1) Aged 20 years and over at the time of consent
  • (2) Able to be hospitalized at the start and the end of study treatment; however, subjects may be treated on both an inpatient and outpatient basis at the time of consent
  • (3) Class I to III according to the World Health Organization (WHO) Pulmonary Hypertension Functional Classification at the time of consent

排除标准

  • (1) Use of catecholamines and/or PDE3 inhibitors for the treatment of cardiac failure at the time of consent
  • (2) Serious cardiac disorder not caused by pulmonary arterial hypertension, such as angina pectoris, myocardial infarction and myocarditis
  • (3) Previous participation in this study

研究者

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