The results, following trials across 34 centres in Japan, Europe, and New Zealand, demonstrate a significant reduction in adverse events for the first time and the clinical advantage of the DynamX Bioadaptor. The data was presented at a late-breaking clinical session during the EuroPCR 2024 conference in Paris.
Shigeru Saito, director of the Division of Cardiology and Catheterisation Laboratory at Shonan Kamakura General Hospital in Japan, said, "These results from the two-year trial are very exciting–unlike anything we’ve ever seen before–and represent a new treatment category for patients living with coronary artery disease. The data shows that the Bioadaptor offers sustained, very low event rates across all major endpoints, making it a superior option compared to DES."
The DynamX bioadaptor is different from current standard-of-care therapies, as it is designed to return vessel health through different phases of adaption in the body to restore vessel biology and maintain consistent blood flow.
"We are beyond thrilled with the findings from the trial," said Motasim Sirhan, CEO of Elixir Medical. "Never before have we seen a vascular technology that addresses the limitations of existing therapies as we have with the DynamX Bioadaptor. These exceptional patient clinical outcomes further validate that the Bioadaptor is truly a transformative technology for the treatment of coronary artery disease."
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