Novel, Long-Term Percutaneous Access Device for Chronic Therapy

Information

  • Research Project
  • 8591332
  • ApplicationId
    8591332
  • Core Project Number
    R44HL107076
  • Full Project Number
    2R44HL107076-02A1
  • Serial Number
    107076
  • FOA Number
    PA-12-088
  • Sub Project Id
  • Project Start Date
    2/7/2011 - 14 years ago
  • Project End Date
    7/31/2015 - 10 years ago
  • Program Officer Name
    BALDWIN, TIM
  • Budget Start Date
    8/26/2013 - 12 years ago
  • Budget End Date
    7/31/2014 - 11 years ago
  • Fiscal Year
    2013
  • Support Year
    02
  • Suffix
    A1
  • Award Notice Date
    8/26/2013 - 12 years ago
Organizations

Novel, Long-Term Percutaneous Access Device for Chronic Therapy

DESCRIPTION: A novel, next-generation percutaneous access device (PAD) focused on pre-emptively reducing catheter related exit site infection will be developed for the delivery of chronic, life-sustaining therapies requiring long- term access through the skin. ViaDerm II uses vacuum assist to remove exudate and proliferate dermal fibroblasts as soon as the catheter penetrates the skin. In addition it uses a device structure enabling stability and a surface treatment, shown to enable cell attachment in preclinical and human studies. The overall goal of this proposal is to develop, test and qualify the ViaDerm II for human use, and commercialize the product globally. ViaDerm LLC intends to enter into strategic partnerships with a market leader in each therapy: cardiac assist, dialysis, and chemo- or other therapies using central venous access. ViaDerm will work with partners to integrate market and sell ViaDerm's value-added technology with their existing and new product lines. ViaDerm II will address the market's expressed unmet need for a long-term, infection-resistant device that is commercially packaged as a sterile, off-the-shelf product. In Phase II, working in conjunction with industry partners, ViaDerm will focus on obtaining regulatory approvals and refine the product design based on initial clinical trial experience. The endpoint of Phase III will be full commercialization of the ViaDerm II in three target markets: cardiac assist, dialysis and central venous access. In parallel, ViaDerm expects to develop additional and new applications, expanding its family of PAD products. The significance and commercial potential of this proposal is substantial. It is estimated that several hundred thousand devices requiring reliable, long-term or prolonged percutaneous access are used every year. These patients suffer from heart failure, renal failure, cancer, and chronic digestive disorders. Foresight Science & Technology, Inc has provided a third party commercial assessment investigating the commercial interest and market impact potential of this technology. Foresight found that the total global addressable market for this technology is approximately US $2.35 billion and estimates ViaDerm LLC year five revenues to approach US $170 million based on 1.7 million units sold worldwide. If successful, this innovative PAD will not only improve the quality of life, reduce medical complications and healthcare costs associated with current therapies, but provide a pre-emptive, infection resistant new skin access option for the development of new emergent therapies.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R44
  • Administering IC
    HL
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    721926
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
    NHLBI:721926\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    VIADERM, LLC
  • Organization Department
  • Organization DUNS
    078309332
  • Organization City
    PLYMOUTH
  • Organization State
    MI
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    481702475
  • Organization District
    UNITED STATES