Jupiter Endovascular Closes Oversubscribed Series B Financing, Surpassing $40 Million Target
Round Led by
The financing comes between two major milestones: FDA 510(k) clearance last month of the Vertex™ Catheter incorporating TFX, and the upcoming presentation of first-in-human results for the Vertex Pulmonary Embolectomy System with TFX from the SPIRARE I trial at the
“Closing this oversubscribed Series B financing round reflects strong conviction in our mission to rewrite the rules of endovascular medicine using TFX technology,” said
SPIRARE I (NCT06571760) is a prospective, single-arm, multicenter study which enrolled 10 subjects with acute, intermediate-risk PE treated with the Vertex Pulmonary Embolectomy System at two sites in
The company is also currently enrolling patients in SPIRARE II (NCT06576427), a prospective, single-arm, multicenter pivotal trial which will enroll up to 145 patients with acute, intermediate-risk PE treated with the Vertex Pulmonary Embolectomy System at up to 25 sites in the
The company’s TFX platform technology, integrated into the Vertex system, is designed to bring a new level of stability and control to a variety of catheter interventions while protecting the cardiovascular anatomy, with the goal of enabling interventionalists to treat anatomical sites that are not safely or easily accessible via conventional endovascular approaches. The Vertex device is delivered in a flexible, relaxed state over a guidewire to a target location in the vasculature, rapidly pressurized with saline to fix it in a stable position for intervention, then returned to its relaxed state to navigate to another target location or for removal.
“Since the earliest days of endovascular medicine, the inability to maintain catheter control has been the single greatest barrier to the wider adoption of transcatheter therapies,” said
About Jupiter Endovascular
Jupiter Endovascular is a medical technology startup developing a new class of endovascular interventions powered by its proprietary Transforming Fixation (TFX) platform technology. The TFX-enabled procedure is designed to bring unmatched stability, control, and anatomical protection to catheter-based therapies. By allowing interventionalists to navigate flexibly through the vasculature and then stabilize with precise control at the treatment site while remaining conformed to the anatomy, Jupiter aims to expand the boundaries of endovascular medicine. Jupiter is initially focused on pulmonary embolism, with plans to expand into additional high-need cardiovascular applications. To learn more, visit www.jupiterendo.com.
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