SBIR-STTR Award

Novel, Long-Term Percutaneous Access Device for Chronic Therapy
Award last edited on: 2/7/23

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$1,764,299
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Daniel Wadsworth

Company Information

L.VAD Technology Inc (AKA: CardioPlus Inc~ViaDerm LLC)

46701 North Commerce Center Drive
Plymouth, MI 48170
   (734) 233-3985
   info@viadermllc.com
   www.lvadtech.com
Location: Single
Congr. District: 06
County: Wayne

Phase I

Contract Number: 1R43HL107076-01
Start Date: 2/7/11    Completed: 7/31/11
Phase I year
2011
Phase I Amount
$308,409
A novel, next-generation percutaneous access device (PAD) will be developed for the delivery of chronic and life-sustaining therapies requiring long-term access through the skin. PAD success requirements include skin tissue integration upon implantation providing the opportunity for prolonged, stable, infection-free access. This new design includes the incorporation of cell proliferative methods, avoiding the use of autologous fibroblast pre-coating associated with the Company's first generation PAD product, ViaDerm". The long-term objective is to develop, evaluate the effectiveness, and gain FDA clearance to commercialize the new ViaDerm-II for mechanical circulatory assistance, chronic peritoneal and hemodialysis catheter therapy, and other chronic venous access catheters used for drug and nutritional therapy. ViaDerm-II will address the market's expressed unmet need for a long-term, infection-resistant device that avoids the need for autologous fibroblast pre-coating, and is commercially packaged as a sterile, ready-to-use, off-the-shelf product. This Phase I application intends to complete the design modifications necessary to incorporate cell proliferative methods and to verify that the design meets its requirements using cell culture and computer modeling techniques. In addition, the new PAD system will be prototyped and surgeon review obtained for animal experiments planned in Phase II. Upon establishing feasibility of the ViaDerm-II concept in Phase I, Phase II of the proposal will focus on refining and evaluating the prototype system design. An appropriate animal model will be used to demonstrate both acute and chronic efficacy. The endpoint of Phase II will include the submission of an IDE application in support of a clinical validation study. The Company believes the healthcare significance and commercial potential to be high. 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, kidney failure, cancer and chronic digestive disorders. If successful, this improved PAD will not only improve the quality of life and reduce complications and costs associated with these existing patients, but provide a new skin access option for new therapies.

Public Health Relevance:
Commercial application of the research extends to chronic and life-sustaining therapies requiring long-term access through the skin, including end stage renal failure, heart failure, and cancer. The research has relevance to an estimated several hundred thousand devices implanted every year that require a reliable, long-term percutaneous access.

Thesaurus Terms:
Acute;Address;Adherence;Adherence (Attribute);Animal Experiments;Animal Model;Animal Models And Related Studies;Autologous;Body Tissues;Cancers;Care, Health;Caring;Catheters;Cell Culture Techniques;Cell Locomotion;Cell Migration;Cell Movement;Cells;Cellular Migration;Chronic;Clinical;Competence;Complication;Computer Simulation;Computerized Models;Delivery Of Health Care;Development And Research;Devices;Digestive Diseases;Digestive System Diseases;Digestive System Disorders;Dressing;Drug Delivery;Drug Delivery Systems;Drug Targeting;Drug Targetings;Drug Therapy;Esrd;Economics;Effectiveness;End Stage Renal Failure;End-Stage Kidney Disease;Environment;Fibroblasts;Generations;Goals;Harvest;Health Sciences, Allied And Health Services Delivery;Healthcare;Healthcare Delivery;Heart Failure;Hemodialyses;Hemodialysis;Human;Human, General;In Situ;In Vitro;Infection;Kidney Failure;Kidney Insufficiency;Left;Legal Patent;Life;Literature;Malignant Neoplasms;Malignant Tumor;Man (Taxonomy);Man, Modern;Marketing;Mathematical Model Simulation;Mathematical Models And Simulations;Mechanics;Medical Device;Metabolic;Methods;Methods And Techniques;Methods, Other;Models, Computer;Modification;Motility;Motility, Cellular;Nutritional Support;Parenteral Nutrition;Patents;Patients;Peritoneal;Peritoneal Dialysis;Pharmacotherapy;Phase;Process;Qol;Qualifying;Quality Of Life;R &D;R&D;Renal Disease, End-Stage;Renal Failure;Renal Insufficiency;Reporting;Research;Resistance;Simulation, Computer Based;Site;Skin;Skin Tissue;Source;Sterile Coverings;Sterility;Surface;Surgeon;System;System, Loinc Axis 4;Techniques;Technology;Time;Tissue Engineering;Tissues;Vacuum;Venous;Ventricular;Wound Healing;Wound Repair;Biomedical Implant;Cardiac Failure;Cell Motility;Commercial Application;Computational Modeling;Computational Models;Computational Simulation;Computer Based Models;Computerized Modeling;Computerized Simulation;Cost;Design;Designing;Digestive Disorder;Engineered Tissue;Fluid Flow;Health Care;Health Care Delivery;Hyperalimentation Therapy;Implant Device;Implantable Device;Implantation;Improved;In Silico;Indwelling Device;Innovate;Innovation;Innovative;Life-Sustaining Therapy;Malignancy;Meetings;Model Organism;Neoplasm /Cancer;Neoplasm/Cancer;Next Generation;Novel;Nutritional Care;Nutritional Therapy;Prototype;Research And Development;Resistant;Scaffold;Scaffolding;Sterile;Success;Tissue Repair;Tissue Scaffold;Tissue Support Frame;Validation Studies;Virtual Simulation;Wound

Phase II

Contract Number: 2R44HL107076-02A1
Start Date: 2/7/11    Completed: 7/31/15
Phase II year
2013
(last award dollars: 2014)
Phase II Amount
$1,455,890

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.

Public Health Relevance Statement:


Public Health Relevance:
In this Phase II SBIR ViaDerm LLC plans to develop and qualify for human use, an innovative percutaneous access device for use in catheter or drive line delivered life-sustaining therapies such as heart failure, dialysis and chemotherapy. Innovation lies in the use of vacuum assist in conjunction with a proprietary percutaneous access device known to encourage device-tissue attachment and accelerated healing. Combined with the use of negative pressure, this innovative second generation complements existing anti-microbial/biofilm approaches to meet an unmet clinical and societal need.

Project Terms:
Address; Animal Model; Animals; antimicrobial; base; Cardiac; Caring; Catheters; Cell-Matrix Junction; chemotherapy; Chronic; Clinical; Clinical Protocols; Clinical Research; Clinical Trials; commercialization; Competence; Complement; Complication; Data; Dermal; design; Development; Devices; Dialysis procedure; Digestive System Disorders; Drug Delivery Systems; Economics; Effectiveness; experience; Exudate; Family; Family suidae; Fibroblasts; Generations; Goals; Healed; healing; Health Care Costs; health care delivery; Heart; Heart failure; Hemodialysis; Human; improved; In Situ; industry partner; Infection; innovation; interest; Kidney Failure; Life; life-sustaining therapy; Literature; Malignant Neoplasms; Marketing; Measures; Mechanics; medical complication; Medical Device; meetings; Microbial Biofilms; Modeling; Modification; next generation; novel; Outcome; Parenteral Nutrition; Patients; Peritoneal Dialysis; Phase; pre-clinical; pressure; Probability; Proliferating; prototype; public health relevance; Qualifying; Quality of life; Recruitment Activity; Reporting; Research; research clinical testing; Resistance; Safety; Sampling; Science; Site; Skin; Small Business Innovation Research Grant; Solutions; Source; Sterile coverings; Sterility; Structure; success; Surface; System; Technology; Testing; tissue culture; Tissues; Vacuum; Venous; Work; wound; Wound Healing