IP Library Granted Patent US 11,160,925
Granted Patent B1
US 11,160,925 · App. 17/179,984 · Granted Nov 2, 2021

Automatic drug delivery system for delivery of a GLP-1 therapeutic

Inventors: Trang Ly (Concord, MA); Matt Rainville (Boxford, MA); M. Thomas Andersen (Highland, UT)
Assignee: INSULET CORPORATION
A61M5/1723A61K38/26A61K38/28A61M5/1408A61M5/14248A61M2205/502A61M2205/52A61M2205/8206A61M2230/201
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Quick Facts
Patent No.
US 11,160,925
App. No.
17/179,984
Granted
Nov 2, 2021
Kind
B1
Abstract

The disclosed embodiments are directed to a wearable automatic drug delivery device configured to provide basal dosing of GLP-1 or co-formulation of GLP-1 and insulin. The size and frequency of the basal doses may be controlled by a medication delivery algorithm resident on the wearable drug delivery device based on a basal dosing history and readings from a continuous glucose monitor monitoring the glucose levels of the wearer of the device.

Claims (55)

1. An automatic drug delivery system comprising:

a wearable drug delivery device comprising:

a controller;

a memory, coupled to the controller and configured to store a basal delivery history;

software, for execution by the controller, the software implementing a medication delivery algorithm;

a single reservoir;

a quantity of a GLP-1 Therapeutic, contained in the single reservoir;

a pump mechanism, controlled by the medication delivery algorithm and in fluid communication with the single reservoir; and

a patient interface, in fluid communication with the pump mechanism;

wherein basal doses of the GLP-1 Therapeutic are delivered to a wearer of the wearable drug delivery device in accordance with a basal delivery schedule, the medication delivery algorithm implementing a method comprising:

retrieving the basal delivery history, the basal delivery history including a predetermined number of basal dosages of GLP-1 Therapeutic delivered over a period of time partitioned into intervals;

evaluating the basal dosages within each interval to obtain an interval profile for each interval indicating the amount of GLP-1 Therapeutic delivered in each basal dosage and a delivery time of each basal dosage;

determining an average interval profile comprising a series of average basal dosages, each having an average delivery time;

evaluating each average basal dosage with respect to other average basal dosages to determine a similarity in the amount of the GLP-1 Therapeutic delivered and a similarity in the corresponding average delivery time;

aggregating average basal dosages meeting an amount similarity threshold and assigning a time range based on a time similarity threshold; and

modifying the basal delivery schedule with an updated amount of the GLP-1 Therapeutic based on the aggregated average basal dosages and an updated delivery time based on the assigned time range.

2. The drug delivery system of claim 1 wherein the medication delivery algorithm can vary the size and timing of the delivery of the doses of the GLP-1 Therapeutic.

3. The drug delivery system of claim 2 , further comprising:

an analyte sensor in communication with the wearable drug delivery device;

wherein the medication delivery algorithm takes as input readings from the analyte sensor to determine the size and timing for delivery of the doses of the GLP-1 Therapeutic.

4. The drug delivery system of claim 3 , wherein the analyte sensor is a CGM sensor and further wherein the medication delivery algorithm varies the size and timing for delivery of the doses of the GLP-1 Therapeutic based on the variations in the glucose level of the wearer as detected by the CGM sensor.

5. The drug delivery system of claim 1 , wherein the GLP-1 Therapeutic is a co-formulation of liraglutide and a U100 rapid-acting insulin mixed in a ratio of between 1.8 and 5.4 mg of liraglutide per 1 ml of the rapid-acting insulin.

6. The drug delivery system of claim 5 , wherein the liraglutide and the rapid-acting insulin are mixed in a ratio of 3.6 mg of liraglutide per 1 ml of the rapid-acting insulin.

7. The drug delivery system of claim 1 , wherein the GLP-1 Therapeutic is a co-formulation of lixisenatide or exenatide and a U100 rapid-acting insulin mixed in a ratio of between 20 and 60 mg of lixisenatide or exenatide per 1 ml of the rapid-acting insulin.

8. The drug delivery system of claim 7 , wherein the lixisenatide or exenatide and the rapid-acting insulin are mixed in a ratio of 40 mg of lixisenatide or exenatide per 1 ml of the rapid-acting insulin.

9. The drug delivery system of claim 1 wherein:

the wearable drug delivery device further comprises a second reservoir and second pump mechanism coupled to the second reservoir;

the first reservoir contains GLP-1;

the second reservoir contains a rapid-acting insulin; and

the medication delivery algorithm controls the first pump mechanism and the second pump mechanism to provide varying co-formulations of GLP-1 and insulin to a wearer of the wearable drug delivery device.

10. The drug delivery system of claim 1 wherein the medication delivery algorithm is configured to calculate a daily basal profile based on the basal delivery history, a blood glucose measurement history, and a meal announcement history.

11. The drug delivery system of claim 10 wherein the daily basal profile is further based on a bolus delivery history.

12. The drug delivery system of claim 1 wherein the GLP-1 Therapeutic is a co-formulation of GLP-1 and rapid-acting insulin.

13. A wearable drug delivery device comprising:

a controller;

software, for execution by the controller, the software implementing a medication delivery algorithm;

a single reservoir;

a quantity of a GLP-1 Therapeutic, contained in the single reservoir;

a pump mechanism, controlled by the medication delivery algorithm and in fluid communication with the single reservoir; and

a patient interface, in fluid communication with the pump mechanism;

wherein basal doses of the GLP-1 Therapeutic and insulin are delivered to a wearer of the wearable drug delivery device as directed by the medication delivery algorithm; and

wherein the medication delivery algorithm is further configured to:

accept an input from the wearer indicating that the wearer has experienced an adverse event;

suspend delivery of the GLP-1 Therapeutic; and

resume delivery of the GLP-1 Therapeutic after a predetermined period of time or when a further input is received from the wearer indicating that the wearer wishes to resume the delivery.

14. The drug delivery system of claim 1 wherein the wearable drug delivery device is further configured to deliver bolus doses of the GLP-1 Therapeutic.

15. A wearable drug delivery device comprising:

a controller;

software, for execution by the controller, the software implementing a medication delivery algorithm;

a single reservoir;

a quantity of a GLP-1 Therapeutic, contained in the single reservoir;

a pump mechanism, controlled by the medication delivery algorithm and in fluid communication with the single reservoir; and

a patient interface, in fluid communication with the pump mechanism;

wherein basal doses of the GLP-1 Therapeutic are delivered to a wearer of the wearable drug delivery device as directed by the medication delivery algorithm; and

wherein the medication delivery algorithm is further configured to modify a basal delivery schedule for delivery of the GLP-1 Therapeutic based on a history of basal doses.

Assignments (2)
SECURITY AGREEMENT SUPPLEMENT FOR INTELLECTUAL PROPERTY Recorded Nov 16, 2022
From: INSULET CORPORATION
To: MORGAN STANLEY SENIOR FUNDING, INC., AS COLLATERAL AGENT
Reel/Frame 061951/0977 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 19, 2021
From: LY, TRANG; RAINVILLE, MATT; ANDERSEN, M. THOMAS
To: INSULET CORPORATION
Reel/Frame 055336/0107 →
Continuity (1)
Provisional Application 63143437 · Jan 29, 2021