Actively Recruiting

Early Phase 1
Age: 18Years - 75Years
All Genders
NCT07392281

Efficacy and Mechanisms of Macitentan for Non-Coronary Obstructive Angina

Led by China-Japan Friendship Hospital · Updated on 2026-02-06

40

Participants Needed

1

Research Sites

104 weeks

Total Duration

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AI-Summary

What this Trial Is About

Angina with non-obstructive coronary arteries (ANOCA) is highly prevalent, impairing quality of life and independently associated with cardiovascular events, yet effective treatments are lacking. The endothelin-1 (ET-1)-endothelin receptor (ETR) system is pivotal in ANOCA pathogenesis. Preclinical studies show that ETR blockade or pericyte-specific knockout of ETA receptor improves coronary microcirculatory function in models of myocardial ischemia-reperfusion and diabetes. Clinical evidence indicates ETR antagonists can enhance microvascular endothelial function and myocardial perfusion in ANOCA patients. However, prior studies diagnosed ANOCA based only on symptoms and angiography without precise microvascular functional assessment. Early ETR antagonists also showed frequent adverse effects (e.g., edema, headache), reducing treatment satisfaction. To address this, the investigators will conduct an open-label, single-center, single-arm trial using invasive coronary microcirculatory function testing to accurately phenotype ANOCA and assess microvascular changes. Patients on standard therapy will receive macitentan-a novel ETR antagonist with improved vasodilatory efficacy and safety-to evaluate its effects on coronary microcirculatory function, angina symptoms, and adverse events. Additionally, the investigators will perform multi-omics profiling (proteomics, transcriptomics, metabolomics) on patient blood samples to identify molecular signatures linked to ANOCA subtypes and treatment response, providing evidence for precision intervention strategies in ANOCA.

CONDITIONS

Official Title

Efficacy and Mechanisms of Macitentan for Non-Coronary Obstructive Angina

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-75 years old
  • Typical angina symptoms
  • No obstructive coronary lesions (coronary stenosis 3450% or FFR 3450.8) confirmed by coronary angiography
  • Coronary microcirculatory function confirmed by pressure wire-based thermodilution technique
  • Signed written informed consent form
Not Eligible

You will not qualify if you...

  • Pregnant or lactating women
  • History of heart attack within the last 90 days
  • Severe heart disease such as moderate to severe heart failure or severe heart valve disease
  • Severe kidney impairment (GFR <30 ml/min/1.73m2)
  • Severe liver disease (Child-Pugh class C)
  • Moderately severe anemia (hemoglobin concentration <90 g/L)
  • Participation in another drug intervention trial within the last 90 days

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

China-Japan Friendship Hospital

Beijing, Beijing Municipality, China, 100029

Actively Recruiting

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Research Team

Y

Yanxiang Gao

CONTACT

J

Jingang Zheng

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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