Long-term Percutaneous Access Device for Home Therapies

Information

  • Research Project
  • 6948586
  • ApplicationId
    6948586
  • Core Project Number
    R44HL078294
  • Full Project Number
    5R44HL078294-03
  • Serial Number
    78294
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/1999 - 25 years ago
  • Project End Date
    5/31/2009 - 16 years ago
  • Program Officer Name
    BALDWIN, TIM
  • Budget Start Date
    9/15/2005 - 19 years ago
  • Budget End Date
    5/31/2009 - 16 years ago
  • Fiscal Year
    2005
  • Support Year
    3
  • Suffix
  • Award Notice Date
    9/12/2005 - 19 years ago
Organizations

Long-term Percutaneous Access Device for Home Therapies

DESCRIPTION (provided by applicant): The goal of this proposal is to finalize the development and begin the commercialization of an advanced percutaneous access device (PAD) appropriate for use in chronic home treatment modalities that require long-term body access, such as heart assist devices for treatment of chronic heart failure, total parenteral nutrition, drug delivery, and ambulatory peritoneal dialysis. The PAD is pre-seeded with autologous fibroblasts derived from a small sample of the recipient's skin. Cell seeding improves the device's clinical performance, creating a seal impervious to fluids and microorganisms and minimizing the risk from infection. The purpose of this project is to develop a new PAD, improving upon the first generation ViaDerm TM PAD that demonstrated multiyear stability in animal studies and has been used with excellent results in a series of 9 patients receiving a heart assist device for a total of 1054 patient days. The in vitro results of Phase I demonstrated that fibronectin provided for the best cell retention on the surface of the PAD, however, were insufficient to conclude which of 2 substrates, polycarbonate or polyurethane, provided for optimal protection of the device/tissue interface. The work under this phase II SBIR will focus on: 1) optimizing the device by finalizing the selection of the substrate for the new device, 2) optimizing the cell seeding process by pre-coating the surface with fibronectin and minimizing the overall time required for preparation of the device to make it commercially attractive. The specific aims are to improve the instrumentation and techniques for PAD preparation and to test the device in a series of long-term animal studies. To commercialize this product, the company plans to enter into strategic partnerships with, or license to, major corporations selling supplies to patients in each market. The new PAD is likely to be a premium product, but its cost will be outweighed by benefits of reduced hospitalization, disability and loss of earnings and by improved quality of life.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R44
  • Administering IC
    HL
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    298360
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
    NHLBI:298360\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    L.VAD TECHNOLOGY, INC.
  • Organization Department
  • Organization DUNS
    926555780
  • Organization City
    DETROIT
  • Organization State
    MI
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    48207
  • Organization District
    UNITED STATES