GLP-1 Basal-Bolus Dosing for Stable Therapy and Fewer Side Effects

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Solution Overview

Problem

Traditional GLP-1 agonist therapies administered as fixed weekly doses may not provide optimal results for all patients, leading to variable efficacy and common gastrointestinal side effects, impacting patient tolerance and adherence.

Innovation Solution

A programmable drug delivery system with a reservoir, pump, controller, and user interface that allows for adjustable basal and bolus dosing of GLP-1 agonists, tailored to patient-specific parameters and real-time glucose readings, enabling flexible and personalized administration.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If fixed weekly doses of GLP-1 agonist are administered, then patient convenience and adherence are improved, but therapeutic efficacy becomes variable and gastrointestinal side effects increase

Engineering Contradiction:
Improvepatient convenience and adherenceVSAvoidtherapeutic efficacy consistency
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The fixed weekly dose is segmented into multiple smaller doses administered throughout the week (daily, twice-weekly, or three-times-weekly dosing regimens). This segmentation maintains patient convenience while improving therapeutic efficacy consistency by providing more frequent, smaller amounts of the medication rather than one large dose, thereby reducing gastrointestinal side effects and maintaining stable drug levels.

Inventive Principle:
Principle #1Segmentation

2Device complexity

If fixed weekly doses of GLP-1 agonist are administered, then dosing simplicity is improved, but gastrointestinal side effects and impact on patient tolerance increase

Engineering Contradiction:
Improvedosing regimen simplicityVSAvoidgastrointestinal side effects
Core Design Contradiction:
Device complexityVSObject-affected harmful factors

Solution Approach 1:

The dosing parameters are changed from a single large weekly dose to multiple smaller doses administered at different frequencies (daily, twice-weekly, or three-times-weekly). This parameter change reduces the peak concentration of the drug in the body, thereby minimizing gastrointestinal side effects while maintaining overall therapeutic efficacy and improving patient tolerance.

Inventive Principle:
Principle #35Parameter changes

3Adaptability or versatility

If fixed weekly doses of GLP-1 agonist are administered, then treatment standardization is improved, but ability to address variable patient needs throughout the dosing period is reduced

Engineering Contradiction:
Improvepersonalized dosing flexibilityVSAvoidtherapeutic efficacy throughout dosing period
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The dosing regimen transitions from a static fixed weekly dose to a dynamic multi-dose schedule that can be adjusted based on patient needs. The system allows for flexible dosing frequencies (daily, twice-weekly, or three-times-weekly) and enables healthcare providers to tailor the regimen to individual patient requirements, thereby improving both adaptability and therapeutic efficacy consistency throughout the dosing period.

Inventive Principle:
Principle #15Dynamics

Data Source

PatentUS20260061118A1Basal bolus treatment devices and methods
Publication Date: 2026.03.05 QUASURAS INC
  • US20260061118A1 patent drawing
  • US20260061118A1 patent drawing
  • US20260061118A1 patent drawing

AI summary

A drug delivery system for administering a GLP-1 agonist therapy includes a reservoir configured to contain a GLP-1 agonist, a pump in fluid communication with the reservoir and configured to deliver the GLP-1 agonist, a controller operatively coupled to the pump, and a user interface operatively coupled to the controller. The controller is programmed to deliver a basal dose of the GLP-1 agonist continuously over a 24-hour period and deliver at least one bolus dose of the GLP-1 agonist in addition to the basal dose. The system allows for independent adjustment of basal and bolus doses based on patient-specific parameters, enabling personalized GLP-1 agonist therapy administration.