Orchestra BioMed Receives FDA Breakthrough Device Designation for AVIM Therapy

Core Insights - The U.S. FDA has granted Breakthrough Device Designation for Orchestra BioMed's AVIM therapy, which aims to manage hypertension in patients at high cardiovascular risk [1][3][6] Regulatory and Clinical Development - The Breakthrough Device Designation is specifically for an implantable system (pacemaker) that delivers AVIM therapy to reduce blood pressure in patients with increased ten-year ASCVD risk and uncontrolled hypertension [2][6] - There are over 7.7 million patients in the U.S. who meet the criteria for this therapy [2][6] - AVIM therapy is currently being evaluated in the BACKBEAT global pivotal study, which is a collaboration between Orchestra BioMed and Medtronic [2][3][7] Market Potential and Collaboration - The collaboration with Medtronic allows for the development and commercialization of AVIM therapy, particularly for patients indicated for pacemakers [7][8] - The Breakthrough Device Designation may facilitate favorable reimbursement pathways, including eligibility for NTAP and TPT under CMS programs [4][11] Clinical Efficacy - Pilot studies have shown that AVIM therapy can lead to significant reductions in blood pressure, with net reductions of 8.1 mmHg in 24-hour ambulatory systolic blood pressure and 12.3 mmHg in office systolic blood pressure at six months [10]