Evaluating the VDyne System for treating severe tricuspid regurgitation

Clinical Safety and Efficacy of the VDyne Transcatheter Tricuspid Valve Replacement System for the Treatment of Tricuspid Regurgitation

This study is testing a new heart valve replacement system to see if it can help people with severe tricuspid regurgitation feel better.

Quick facts

• Phase: NA
• Study type: Interventional
• Enrollment: 30 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: VDyne, Inc. (industry)
• Locations: 11 sites (Los Angeles, California and 10 other locations)
• Trial ID: NCT05848284 on ClinicalTrials.gov

What this trial studies

This clinical study aims to assess the safety and effectiveness of the VDyne Transcatheter Tricuspid Valve Replacement System in patients suffering from symptomatic severe tricuspid regurgitation. Participants will be evaluated for their suitability based on specific inclusion criteria, including their NYHA class and response to prior heart failure treatments. The study will involve a heart team that determines the appropriateness of the VDyne System for each patient, ensuring a tailored approach to treatment.

Who should consider this trial

Good fit: Ideal candidates are adults over 18 with symptomatic severe tricuspid regurgitation who have not responded adequately to medical therapy.

Not a fit: Patients with unsuitable cardiac anatomy for the VDyne System or severe left ventricular dysfunction may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could significantly improve the quality of life for patients with severe tricuspid regurgitation.

How similar studies have performed: Other studies have shown promise in transcatheter valve replacement approaches, suggesting potential for success with this novel intervention.

Eligibility criteria

Inclusion Criteria:

* Symptomatic severe tricuspid valve regurgitation of primary or secondary etiology.
* NYHA class ≥ II. If NYHA Class IV, patient must be ambulatory.
* Subject is adequately treated with medical therapy for heart failure ≥ 30 days prior to
* index procedure, including a diuretic.
* Heart Team determines patient is a recommended candidate for the VDyne System.
* Age \>18 years at time of index procedure.
* Clinical Screening Committee (CSC) and Imaging Core Labs confirm suitability for treatment with the VDyne System.

Exclusion Criteria:

* Patient anatomy (cardiac and vascular) is not suitable for VDyne System as assessed by Imaging Core Labs, Sponsor or Clinical Screening Committee (CSC)
* Intolerance to procedural anticoagulation or post-procedural antiplatelet/ anticoagulation regimen that cannot be medically managed
* Hypersensitivity to nickel or titanium
* Left Ventricular Ejection Fraction (LVEF) \<30%.
* Severe RV dysfunction.
* Significant abnormalities of the tricuspid valve and sub-valvular apparatus.
* Sepsis including active infective endocarditis (IE) (within last 6 months).
* Right ventricular, atrial thrombus, vegetation or mass on tricuspid valve.
* Severe tricuspid annular or leaflets calcification.
* Systolic pulmonary hypertension with systolic pulmonary artery pressure \>70 mmHg.
* History or rheumatic fever
* Significant coronary artery disease requiring treatment such as symptomatic, unresolved multi-vessel or unprotected left main coronary artery disease.
* Any planned surgery or interventional procedure within 30 days prior to or 30 days following the implant procedure. This includes any planned concomitant cardiovascular procedure such as CABG, PCI, pulmonary vein ablation, left atrial appendage occlusion, septal defect repair, etc.
* Unresolved severe symptomatic carotid stenosis (\> 70% by ultrasound).
* Cardiac resynchronization therapy device or implantable pulse generator implanted within 60 days of planned implant procedure.
* Permanent pacing leads that will interfere with delivery or implantation of the VDyne Valve.
* Cardiogenic shock or hemodynamic instability requiring inotropes or mechanical support devices at the time of planned implant procedure.
* Prior tricuspid valve surgery or catheter-based therapy with permanent residual device(s) implanted that would preclude delivery or implantation of the VDyne Valve (e.g. valve replacement, edge to edge repair, etc.).
* Significant valvular heart disease requiring intervention other than the tricuspid valve.
* Known significant intracardiac shunt (e.g. septal defect)
* Cerebrovascular accident (stroke, TIA) within 6 months of treatment procedure.
* Severe lung disease (severe COPD or continuous use of home oxygen or oral steroids).
* Acute myocardial infarction (AMI) within 30 days.
* Significant renal dysfunction (eGFR\<30 ml/min/1.73m2) or on dialysis.
* End-stage liver disease (MELD \> 11 / CHILD class C).
* Bleeding requiring transfusion within prior 30 days.
* Coagulopathy or other clotting disorder that cannot be medically managed.
* Chronic immunosuppression or other condition that could impair healing response.
* Any of the following: leukopenia, chronic anemia (Hgb \< 9), thrombocytopenia, history of bleeding diathesis, or coagulopathy.
* Unwilling to receive blood products.
* Known hypersensitivity or contraindication to procedural or post-procedural medications (e.g., contrast solution) which cannot be adequately managed medically.
* Life expectancy less than 12 months due to non-cardiac comorbidities.
* Treatment is not expected to provide benefit (futile).
* Current IV Drug user (must be free drug abuse for \> 1 year).
* Pregnant, lactating or planning pregnancy within next 12 months.
* Vulnerable patient groups (minors, cognitively impaired persons, prisoners, persons whose willingness to volunteer could be unduly influenced by the expectation of benefits associated with participation or of retaliatory response from senior members of a hierarchy in case of refusal to participate, such as students, residents, and employees).
* Currently participating in an investigational drug or device trial that has not reached its primary endpoint or is likely to interfere with this study.
* Patient (or legal guardian) unable or unwilling to provide written, informed consent before study enrollment.
* Patient unable or unwilling to comply with study required testing and follow-up visits

Where this trial is running

Los Angeles, California and 10 other locations

• Cedars-Sinai Medical Center — Los Angeles, California, United States (RECRUITING)
• Henry Ford Hospital — Detriot, Michigan, United States (RECRUITING)
• Minneapolis Heart Institute Foundation — Minneapolis, Minnesota, United States (RECRUITING)
• Mayo Clinic - Rochester — Rochester, Minnesota, United States (RECRUITING)
• Columbia University Medical Center/NYPH — New York, New York, United States (RECRUITING)
• Montefiore Medical Center — The Bronx, New York, United States (RECRUITING)
• The Christ Hospital — Cincinnati, Ohio, United States (RECRUITING)
• Oregon Health and Science Unversity — Portland, Oregon, United States (RECRUITING)
• Medical University of South Carolina — Charleston, South Carolina, United States (RECRUITING)
• Ascension St. Thomas — Nashville, Tennessee, United States (RECRUITING)
• Québec-Université Laval (IUCPQ-ULaval) — Québec, Quebec, Canada (RECRUITING)

Study contacts

• Study coordinator: Vinny Podichetty

Conditions: Tricuspid Regurgitation, Tricuspid Valve Disease, Tricuspid Valvular Disorders, VDyne