Actively Recruiting
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
On this page
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
Eligibility Criteria
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
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
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
China-Japan Friendship Hospital
Beijing, Beijing Municipality, China, 100029
Actively Recruiting
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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