Healthcare Industry News: dilatation catheter
News Release - May 10, 2012
Cardionovum(R) Will Launch Two Drug-Eluting Balloon (DEB) Dilatation Catheter Product Families at EuroPCR 2012“We have opened a whole new dimension for the clinically advanced treatment of coronary and endovascular artery disease.”
- Dr. Michael Orlowski, CEO
Booth F23, Palais des Congrès, Paris
BONN, Germany--(Healthcare Sales & Marketing Network)--Cardionovum GmbH will launch two drug-eluting balloon (DEB) dilatation catheter product families at next week’s EuroPCR 2012 congress: Paclitaxel-coated drug-eluting balloons for (1) coronary (PRIMUS®) and (2) peripheral (LEGFLOW®) applications.
With the proprietary Cardionovum gradient balloon coating technology, nanocrystalline Paclitaxel is embedded only under the surface of the top layer of a newly formulated shellolic acid drug-release-matrix. Efficient drug release, reproducibility and clinically superior drug in-tissue availability have been conclusively demonstrated in GLP preclinical trials. (Note: shellolic acid is FDA-cleared under category ‘E 904’ as a food additive. It is a natural resin, which is often applied in the pharmaceutical industry for film-coating of pills for control of pill dissolution.)
Preclinical testing was performed at CV Path Institute (Gaithersburg, USA) and validated that Cardionovum’s DEB coating does not cause any noticeable micro-emboli, which classifies Cardionovum’s DEBs to be as safe as any uncoated angioplasty balloon catheter relative to potential micro-embolies. Both safety features, integrity of the drug coating composition and non-occurrence of micro-emboli, increase the safety profile for operators and patients and fulfill safety requirements of regulatory authorities.
Cardionovum holds worldwide multiple priority patent-pending rights for its coating technology.
The Company’s product pipeline includes: (1) Paclitaxel-coated RESTORE® DEB, a novel drug-carrier-matrix that enables increased drug-in-tissue concentration, which is designed to widen the therapeutic window and result in an improved outcome for most patients with critical limb ischemia (CLI) and diabetic foot syndrome (DFS), as well as patients who have to undergo repeated interventions (e.g., diabetic patients) and patients with dialysis fistula stenosis. (2) Sirolimus-coated RENERGY® DEB, for which it has been demonstrated conclusively in preclinical trials that this technology overcomes the commonly known difficulty of achieving a therapeutically effective drug-in-tissue concentration of Sirolimus with DEB. (3) A drug-eluting aortic valvuloplasty (DAVY) balloon catheter featuring a new formulation for ultra-fast drug-elution in just four seconds to the ring of the aortic valve for the treatment of patients for whom TAVI is counter-indicated or to delay the necessity for valve replacement by TAVI or open surgery.
Based on its breakthrough and proprietary PTX coating technology, Cardionovum has developed and is commercializing in Europe clinically advanced medical therapies that improve upon current patient treatment standards for drug-eluting stents and balloons to treat coronary and vascular artery disease.
NOTICE: Cardionovum’s products are not available for sale in the United States.
Issuer of this News Release is solely responsible for its
Please address inquiries directly to the issuing company.