You are here

Development of a miniaturized single-port automated insulin delivery system utilizing a glucose sensing catheter, ultra-concentrated insulin, and an optimized control algorithm

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 2R44DK123766-02
Agency Tracking Number: R44DK123766
Amount: $1,497,939.00
Phase: Phase II
Program: SBIR
Solicitation Topic Code: 200
Solicitation Number: DK19-027
Timeline
Solicitation Year: 2019
Award Year: 2021
Award Start Date (Proposal Award Date): 2021-07-16
Award End Date (Contract End Date): 2023-06-30
Small Business Information
2828 SOUTHWEST CORBETT AVE STE 211A
Portland, OR 97201-4811
United States
DUNS: 078297084
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 THOMAS SEIDL
 (971) 340-5601
 tseidl@pacificdt.com
Business Contact
 ROBERT CARGILL
Phone: (971) 340-5601
Email: bcargill@pacificdt.com
Research Institution
N/A
Abstract

ABSTRACT
Significance: There are over 5 million people with insulin-treated diabetes in the United States who represent
a disproportionately large share of the $237B in direct medical costs attributable to diabetes. The use of
continuous glucose monitoring (CGM) has been shown to reduce HbA1c levels, a proven predictor of health
outcomes within this population, with the greatest improvement achieved when CGM is coupled with
continuous subcutaneous insulin infusion (CSII). The recent convergence of CGM and insulin pumps has
enabled the first generation of automated insulin delivery (AID) systems, promising even better glycemic
control for insulin-treated diabetes. However, current AID systems are complex, cumbersome, and expensive
for the patient because they require multiple devices to be worn on the body: a glucose sensor, an insulin
pump, and an insulin delivery catheter. We have developed a glucose sensing catheter that reduces the
number of subcutaneous components from two to one, significantly reducing the size and complexity of these
systems. The PDT interoperable sensing cannula assembly that we are proposing to commercialize in this
phase 2 SBIR will allow any insulin patch pump manufacturer to rapidly integrate CGM directly on the insulin
delivery cannula, thereby enabling people with T1D who are patch pump users to effortlessly utilize CGM
through a single subcutaneous injection site. Importantly, this platform will also improve AID system reliability
and security by replacing the wireless communication from CGM to pump controller with a direct wired
connection. Resulting reductions in system size, complexity, and cost will increase adoption rates for pump
user and people using AID, helping improve compliance, lower HbA1c levels, and improve health outcomes
among people with type 1 diabetes. Preliminary Data: PDT has recently demonstrated that delivering insulin
at the site of glucose sensing is possible using a patented redox mediator-based sensing cannula. However,
we have also shown that there is a dilution artifact that occurs immediately after a dose of insulin is delivered
through the cannula. We have shown that this artifact is independent of whether insulin or saline is delivered.
In Phase 1 of this SBIR, we demonstrated in a swine study that this artifact is related to the size of the bolus.
We further demonstrated that the artifact can be significantly reduced by using higher concentration insulin and
ultimately eliminated by using sophisticated predictive signal processing methods. Specific Aims: In Phase 2
of this project, we will use the products of Phase 1 to take the next logical steps in integration of our sensing
cannula into a dual function patch pump platform. In Specific Aim 1, we will further characterize and evaluate
the accuracy of the PDT sensing cannula in a human study. In Specific Aim 2, we will work with a commercial
pump partner (EOFlow) to develop and evaluate an interoperable sensing cannula assembly (ISCA) that is
designed for rapid integration into a patch pump. The ISCA will include the required electronics, mechanical
components, and a software development kit that will enable rapid integration into commercial patch pumps.
Working with our academic partners at OHSU, we will transfer the artifact elimination predictive signal
processing algorithm and port this algorithm to the ISCA for use in real-time operation. In Specific Aim 3, we
will integrate the sensor assembly into our commercial partner’s patch pump and validate the performance and
accuracy of the design in a swine study. At the conclusion of Phase 2, we will have a dual-function glucose-
sensing patch pump validated in a swine study and poised to enter clinical study. In Phase 2B, we will conduct
those studies, and work with our academic collaborators and commercialization partners to incorporate a
model predictive controller into the patch pump to yield an all-in-one automated insulin delivery solution.

* Information listed above is at the time of submission. *

US Flag An Official Website of the United States Government