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To view or add a comment, sign in VDYNE Received US FDA Approval to Initiate TRIVITA1 IDE Pivotal Trial of Transcatheter Tricuspid Valve Replacement System * VDYNE received US FDA approval for an IDE to start the TRIVITA1 pivotal trial of its transcatheter tricuspid valve replacement system * The trial targeted leading US clinical centers to assess the system’s safety and effectiveness in patients with severe tricuspid regurgitation * VDYNE’s CEO highlighted the milestone as a key step toward addressing unmet needs in tricuspid regurgitation treatment * The approval marked progress in developing next-generation valve technologies for improved patient outcomes #MedTech #FDA #MedicalDevices #ClinicalTrials #TricuspidValve #CardioInnovation #HealthTech VDyne To view or add a comment, sign in If you use peptides clinically, the biggest move this week was not a new study