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Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- Biotex, Inc.
- Proposal award date
- 2020-07-24
- Contract end date
- 2022-06-30
- UEI
- SUH7H6LEZTS2
- Solicitation number
- PA19-272
- Topic code
- NHLBI
Research abstract
Project Summary/AbstractThe overall goal of this Direct to Phase II SBIR proposal is to develop the Ark, a novel device for
providing improved access, protection, and functionality during placement of hemodialysis needles. In
the US alone, over 700,000 patients receive hemodialysis treatment, and creation of an arteriovenous
fistula (AVF) and access vein is the preferred access point for dialysis needles. Most access veins suffer
from the following shortcomings: long waiting periods to mature; challenging to access; prone to damage
by needle penetration through the vessel; and limited useful life, failing largely because of both excessive
and poor punctures. As a result, many dialysis patients do not receive the treatment required for
continued quality of life.The Ark is designed to remediate the limitations of the current practice and aid long-term use of
access veins. The Ark is intended for surgical implantation around the access vein, ideally at the time of
AVF creation. The infrastructure promotes ingrowth of surrounding soft tissues reinforcing the strength
of the vein, while providing an opening for easy needle access and a back wall for vessel protection
from inadvertent penetration. The implant provides a palpable structure beneath the skin, promoting
more accurate needle puncture, improving both caregiver efficacy and patient comfort. Initial prototypes
of the Ark have gone through preliminary benchtop and animal studies demonstrating feasibility and
significant promise. Continued efforts will build on these results to optimize the design, perform
cannulation studies in a relevant AVF animal model, complete required design controls and validation
activities, and perform a chronic GLP study, supporting a planned submission for FDA Clearance. We
expect the end result of this effort will greatly facilitate the move toward home-based dialysis, resulting
in significant impact on patient health and health care cost savings.Project NarrativePatients with chronic kidney disease must undergo hemodialysis a minimum of three times per
week for up to four hours per treatment, but more frequent dialysis results in a significant improvement
in their quality of life. Increasing the treatment frequency comes with its own set of complications,
including: increased risk of infiltration, weakening of the vessel wall at the access site, and low blood
flow from collapsing vessels, among other factors leading to failure of the access vein. The Ark is
intended to improve access, eliminate the need for excessive punctures, and prevent penetration of
vessel side and back walls, ultimately lengthening the useful life of the access vein and restoring the
ongoing quality of life of long-term dialysis patients.
Technology keywords
Not reported
Other awards by this recipient
Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.
Awards with the same topic code
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Research funding history
60 SBIR/STTR records share this UEI (1997–2025). Reported award amounts total $24,544,336. Reported amounts are not federal obligations.
Phases: Phase I, Phase II, Phase II – Direct to Phase II
Agencies: Department of Health and Human Services, Environmental Protection Agency, Department of Defense, National Science Foundation, Department of Agriculture, National Aeronautics and Space Administration
Agency intelligence
Department of Health and Human Services
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