Surmodics Announces SWING Trial 24-Month Data To Be Presented At VEITHsymposium On November 15

Surmodics, Inc. (NASDAQ:SRDX), a number one supplier of medical machine and in vitro diagnostic applied sciences to the well being care business, introduced right this moment that Professor Ramon Varcoe will current 24-month knowledge from the SWING Trial, a first-in-human examine of the protection and efficiency of the Sundance™ Sirolimus Drug-Coated Balloon (DCB). The session will likely be held on Wednesday, November 15th, on the 50th annual VEITH Symposium in New York, New York.

TITLE: 2-12 months Outcomes With The Sundance DCB (Surmodics) To Deal with BTK Occlusive Lesions: From The SWING Trial
DATE: Wednesday, November 15
TIME: 9:18 – 9:23 AM (EST)
VENUE: New York Hilton Midtown, Grand Ballroom East, third Ground

Professor Varcoe, MBBS, MS, FRACS, PHD, MMed (ClinEpi), co-lead investigator of the SWING Trial, is a vascular surgeon at Sydney’s Prince of Wales and Prince of Wales Hospital the place he’s Director of Working Theatres, and Director of Surgical procedure and Anesthetics for the South East Sydney Well being District. He’ll assessment security and efficiency knowledge collected by means of 24 months of follow-up for 35 topics with occlusive illness of the infra-popliteal arteries who had been handled at examine websites in Australia, New Zealand, and places in Europe. Research topics will likely be adopted for 36 months after the index process.

Professor Varcoe beforehand introduced SWING Trial 12-month knowledge on January 18th on the thirty fifth Annual Worldwide Symposium on Endovascular Remedy (ISET) convention. An 8.3% charge of main antagonistic occasions was reported within the per protocol (PP) inhabitants (two clinically pushed goal limb revascularizations) at 6 months, with no further antagonistic occasions reported for PP topics within the 12-month knowledge. Goal lesion major patency charge, outlined as freedom from goal vessel occlusion or goal lesion revascularization related to deterioration or Rutherford Medical Classification and/or enhance in dimension of pre-existing wounds (or incidence of recent wounds), and lesion restenosis >50%, was 80% at 12 months within the PP inhabitants.

The Sundance Sirolimus Drug-Coated Balloon makes use of a next-generation coating expertise consisting of microcrystalline sirolimus and a proprietary excipient designed to maximise drug switch, enhancing sirolimus supply and sustaining therapeutic ranges within the artery. Sirolimus, a potent anti-inflammatory and anti-proliferative compound, has been used efficiently in coronary drug-eluting stents. The supply of sirolimus to the vessel wall throughout mechanical balloon dilatation offers an ancillary motion of inhibiting the proliferation of cells, with the supposed function of lowering restenosis. The Sundance Sirolimus Drug-Coated Balloon will not be obtainable on the market anyplace on the planet, and at the moment is for investigational use solely.

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