Endothelial Cell Activation and Total Pulmonary Resistance in PAH

Launched by IMPERIAL COLLEGE LONDON · Sep 6, 2023

Keywords

ClinConnect Summary

This clinical trial is investigating how changes in the health of blood vessel cells (known as endothelial cells) may relate to the overall resistance of blood flow in the lungs for people with pulmonary artery hypertension (PAH). PAH is a serious condition where the blood vessels in the lungs are narrowed, making it harder for blood to flow and leading to various symptoms. The trial aims to see if monitoring these changes can help us understand and possibly improve the treatment of PAH.

To participate in this study, individuals need to be between 18 and 75 years old and diagnosed with PAH under specific categories, such as idiopathic PAH or PAH associated with certain diseases. Participants should also have stable PAH symptoms and be on a consistent treatment plan for at least a month. Before joining, participants will need to provide written consent and may undergo tests to ensure their eligibility. Throughout the study, participants will be monitored using special devices that track their heart and lung health. This trial is currently not recruiting, so interested individuals should stay tuned for updates on when it will begin.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Subjects aged between 18-75 years old
• • 2. PAH which is: idiopathic; PAH heritable; PAH associated with connective tissue disease; PAH after ≥ 1 year repair of congenital systemic to pulmonary shunt; or PAH associated with anorexignes or other drugs.
• • 3. Resting mean pulmonary artery pressure ≥25 mmHg, pulmonary capillary wedge pressure ≤15 mmHg, PVR \>5 wood units, and normal or reduced cardiac output, as measured by a previous right heart catheterisation (RHC).
• • 4. Have an insertable FDA/CE cardiac rhythm monitor and pulmonary artery pressure monitor that captures cardiopulmonary haemodynamics and daily activity.
• • 5. Six-minute walking distance \>50m at entry
• • 6. Stable on an unchanged PAH therapeutic regime comprising at least 2 therapies licensed for PAH (any combination of endothelin receptor antagonist, phosphodiesterase inhibitor or prostacyclin analogue) for at least 1 month prior to screening
• • 7. Subjects willing to be genotyped for genes that influence XBD173 activity
• • 8. Able to provide written informed consent prior to any study mandated procedures
• • 9. Contraception: Fertile females (women of childbearing potential) are eligible to participate after a negative highly sensitive pregnancy test, if they are taking a highly effective method of contraception other than the oral contraceptive pill during treatment and until the end of relevant systemic exposure
• Exclusion Criteria:
• • 1. Unable to provide informed consent and/or are non-fluent speakers of the English language
• • 2. Hypersensitivity to XBD173 or to any of the excipients
• • 3. Clinically-significant renal disease (confirmed by creatinine clearance \<30 ml/min per 1.73m2)
• • 4. Clinically-significant liver disease (confirmed by serum transaminases \>2 times than upper normal limit)
• • 5. Anaemia confirmed by haemoglobin concentration \<10 g/dl
• • 6. Individuals known to have haemoglobinopathy sickle cell disease, thalassaemia
• • 7. Hospital admission related to PAH or change in PAH therapy within 3 months prior to screening
• 8. History of left-sided heart disease and/or clinically significant cardiac disease, including but not limited to any of the following:
• • 1. Aortic or mitral valve disease (stenosis or regurgitation) defined as greater than mild aortic insufficiency, mild aortic stenosis, mild mitral stenosis, moderate mitral regurgitation
• • 2. Mechanical or bioprosthetic cardiac valve
• • 3. Pericardial constriction, effusion with tamponade physiology, or abnormal left atrial size.
• • 4. Restrictive or congestive cardiomyopathy
• • 5. Left ventricular ejection fraction ≤50% (measured in echocardiogram at screening)
• • 6. Symptomatic coronary disease
• • 7. Significant (2+ for regurgitation) valvular disease other than tricuspid or pulmonary regurgitation
• • 8. Acutely decompensated left heart failure within 1 month of screening
• • 9. History of untreated obstructive sleep apnoea
• • 9. Evidence of significant lung disease on high-resolution CT (if available) or recent (performed within 12 months) lung function, where FEV1 \< 50% predicted and FVC \< 70% predicted, and DLCO (or TLCO) \< 50% predicted if any CT abnormalities; judged by the Site Physician
• • 10. Patients with a history of uncontrolled systemic hypertension
• • 11. Acute infection (including eye, dental, and skin infections)
• • 12. Chronic inflammatory disease including HIV, and Hepatitis B
• • 13. Women of childbearing potential who are pregnant or breastfeeding (if applicable)
• • 14. Patients who have received an Investigational Medicinal Product (IMP) within 5 half-lives of the last dose of the IMP or 1 month (which ever is greater) before the baseline visit