A transcatheter functional valve replacement for tricuspid valve insufficiency

Informazioni relative al progetto

Trillium

ID dell’accordo di sovvenzione: 190109977

DOI

10.3030/190109977

Progetto chiuso

Data della firma CE 8 Luglio 2022

Data di avvio 1 Giugno 2022

Data di completamento 31 Maggio 2026

Finanziato da

• The European Innovation Council (EIC)

Costo totale

€ 5 525 003,75

Contributo UE

€ 2 500 000,00

Coordinato da

INNOVENTRIC LTD
Israel

Periodic Reporting for period 2 - Trillium (A transcatheter functional valve replacement for tricuspid valve insufficiency)

Periodo di rendicontazione: 2023-10-01 al 2025-01-31

Sintesi del contesto e degli obiettivi generali del progetto

Tricuspid regurgitation (“TR”) is a frequent disease with a graded increase in mortality as disease severity increases. The “still forgotten” TR patient population is ineligible for surgical or transcatheter on-valve treatments. This includes >40% of patients with challenging anatomy, lead-induced TR, failed prior tricuspid repair, poor tricuspid valve echo imaging, and prohibitive risk for TEE and GA. These patients have no treatment option with the current or pipeline transcatheter tricuspid valve therapies.

The Trillium™ offers ALL of these patients a simple, safe, and efficacious solution. The Trillium™ is a truly innovative heterotopic cross-caval tricuspid valve replacement specifically designed for the tricuspid valve environment. The Trillium™ is a stent graft with a valved wall that spans the right atrium with one end fixated in the SVC and the other end fixated in the IVC. The Trillium™ offers treatment for TR while leaving the native valve untouched. The procedure is simple, takes less than 10 minutes, and does not require Echo guidance or General anesthesia.

Lavoro eseguito dall’inizio del progetto fino alla fine del periodo coperto dalla relazione e principali risultati finora ottenuti

160 devices were produced for various applications, including V&V testing, pre-clinical trials on the swine model, Biocompatibility lab testing, Sterilization validation protocols, LAL, and bioburden test for clean production zone monitorization.
Enrolment of 20 patients for the Trillium FIH study was completed in June 2023; by then, the Trillium™ had been implanted in 34 patients. In December 2024, The Trillium™ received FDA approval to initiate an EFS trial in the US were 15 patients will be enrolled for the trial, following a successful, Innoventric is is submitted for an IDE-Pivotal study as its next sizeable pivotal study in Europe and the US. Currently, the ESF study shows good results and progressing as planned.

Progressi oltre lo stato dell’arte e potenziale impatto previsto (incluso l’impatto socioeconomico e le implicazioni sociali più ampie del progetto fino ad ora)

The Trillium™ technology has unique benefits for patients and physicians:
• Capable of treating the widest TR patient population
• <10 minutes device implantation time
• No migration
• No leaks
• No need for echo guidance
• No need for rapid pacing
• No need for General Anastasia

To ensure further uptake and success, Trillium™ technology needs to be further validated through the EFS study as a complementary step in assessing the Trillium™ final design before the commencement of a wide pivotal study in Europe and the US.

FDA approval of our IDE application for the Trillium™ EFS

Successful patient enrollment for Trillium™ FIH study

Successful Series B Funding