Drug Eluting Stent Graft For Treatment Of AAA

Information

  • Research Project
  • 6444152
  • ApplicationId
    6444152
  • Core Project Number
    R43HL069621
  • Full Project Number
    1R43HL069621-01
  • Serial Number
    69621
  • FOA Number
  • Sub Project Id
  • Project Start Date
    2/11/2002 - 23 years ago
  • Project End Date
    7/31/2002 - 22 years ago
  • Program Officer Name
    LUNDBERG, MARTHA
  • Budget Start Date
    2/11/2002 - 23 years ago
  • Budget End Date
    7/31/2002 - 22 years ago
  • Fiscal Year
    2002
  • Support Year
    1
  • Suffix
  • Award Notice Date
    2/12/2002 - 22 years ago

Drug Eluting Stent Graft For Treatment Of AAA

DESCRIPTION (provided by applicant): Abdominal aortic aneurysms (AAA) affect approximately two percent of women and five percent of men over age sixty five, and are almost certainly fatal if allowed to rupture. Although surgery involving vascular grafts or endovascular graft systems is widely accepted as a standard treatment for AAA, new, minimally invasive stent grafting technologies are rapidly entering the market. Stented aneurysms are, however, like stented postangioplasty arteries, subject to thrombolysis and restenosis. Heparin and Heparin derivatives are commonly used to treat thrombolysis; several pharmacotherapeutic agents are claimed to control restenosis. Implant Sciences proposes to improve drug delivery to AAA sites by incorporating Heparin and a restenosis-inhibiting drug into a non-erodable, biodurable-polyurethane graft-coating. Rapamycin, based on its success in recently completed and highly publicized clinical trials when delivered from an eluting stent directly to percutaneous coronary revascularization sites, is the inhibitor of choice. To sequester the drugs, an eluting polymer currently marketed in Europe as VascuLink will be employed. By substituting for systemic drug administration localized, time-release, multi-drug delivery via a coated-stent, the proposed device not only affects a lifesaving repair but also, by minimizing Heparin and Rapamycin doses, reduces the potential for adverse side effects. PROPOSED COMMERCIAL APPLICATION: Although endovascular repair of AAA is not likely to replace surery, it can be extended to many patients who were previously considered poor surgical candidates. Compared to open surgery the hospital stay and the recovery times are shorter, both perceived positively by the patient (improved quality of life) and by the healthcare system (cost effectiveness). With the population aging and approximately 100,000 new AAA cases diagnosed every year, the commercial potential is significant, and, with the newer, improved devices, will become even more so.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R43
  • Administering IC
    HL
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    99917
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
    NHLBI:99917\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    IMPLANT SCIENCES CORPORATION
  • Organization Department
  • Organization DUNS
  • Organization City
    WAKEFIELD
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    01880
  • Organization District
    UNITED STATES