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Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- Capillary Biomedical, Inc.
- Proposal award date
- 2018-08-01
- Contract end date
- 2019-07-31
- UEI
- MHJQM57VPFV5
- Solicitation number
- PAR17-034
- Topic code
- 200
Research abstract
PROJECT SUMMARYABSTRACT
Capillary Biomedical Incis developing an infusion setcatheter cannula inserterfor the
treatment of diabetes mellitus with continuous subcutaneous insulin infusionCSIIThe
Capillary infusion cannula has been reinvented to include kink resistancean internal
reinforcing coilmultiple outlet portsan `effortlessandaposautomatic inserter and other performanceimproving design elementsThis combination of features will remove barriers to CSII therapy by
increasing the infusion set replacement interval beyond the currenttoday standardIt will
also substantially reduce the incidence of very commonand frustratingfailure modes that
impact the health of diabetic personsincludinginfusion set failure upon insertionblocked
insulin delivery due to kinking or occlusionand infusion site reactionsThis NIH phasegrant proposal addresses exploratory research objectives to study how the
novel design of the Capillary infusion set reduces the failure rate and why it may be safe to
extend continuous use of one Capillary infusion set for up todaysThis project consists of
extensive in vitro and in vivo testing to ensure safety and reliability with the objectives ofFabricating Coil Reinforced Soft Polymer CSII Sets
The Capillary CSII Set design and pilot scale production process will be finalized to produce a
minimum ofcompleted infusion sets suitable for human useVerifying Insulin Compatibility OverDay Duration
We will demonstrate the compatibility of our infusion set in non clinical testing with HumalogInsulin LisproLillyand NovologInsulin AspartNovoto prepare for the human trialClinical Trial to Assess the Capillary Infusion Set Performance in Humans
A twenty five adult patient phaseb inpatient hyperinsulinemia euglycemia study in typediabetics will be conducted in a randomized sequencecross over design to explore
bioavailability and dose response profiles of commercially available rapid acting insulin when
delivered using a CSII pump plus investigational Capillary catheter vs a commercially available
Tefloncatheter fordaysThe proposed primary endpoint is insulin bioavailabilityAUCon the day of insertion PROJECT NARRATIVEPUBLIC HEALTH STATEMENT
Emerging artificial pancreas systems pair a continuous glucose monitor with an insulin
pump and promise to simplify the lives of overM people with Typediabetes in the
United StatesA key barrier to broader adoption of these systems is the day to day
variability in insulin response and theday limit on use of current insulin infusion
cathetersThis research aims to assess the relative bioavailability of subcutaneously
infused insulin using Capillary Biomedicalandapos s investigational infusion set vsa
commercially available infusion set as controlfor up todays extended use
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
Verified by an exact topic code match. This is not a text-similarity match.
Research funding history
2 SBIR/STTR records share this UEI (2016–2018). Reported award amounts total $2,018,977. Reported amounts are not federal obligations.
Phases: Phase II, Phase I
Agencies: Department of Health and Human Services
Agency intelligence
Department of Health and Human Services
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