drugset / Trial / NCT06046417

A Fully Automated Lyumjev and Pramlintide Delivery System for Adults With Type 1 Diabetes

NCT06046417

RandomizedCrossoverOpen-labelTreatment

Summary

The aim of this clinical trial is to investigate whether a fully automated Lyumjev-and-pramlintide delivery system improves glycemic outcomes in adults with type 1 diabetes. The main question we aim to answer is whether a Lyumjev-pramlintide fully closed loop system improves time in range compared to a hybrid closed loop system with carbohydrate counting. We also aim to find the optimal insulin to pramlintide ratio for glycemic control in the fully automated system. In this cross-over study, patients will undergo the following three interventions in a random order: (i) fully automated Lyumjev insulin-and-pramlintide (8 μg/u) (ii) fully automated Lyumjev insulin-and-pramlintide (10 μg/u) (iii) rapid automated Lyumjev insulin-and-placebo with carbohydrate-matched boluses For all interventions, participants will be required to wear two Ypsomed pumps programmed by our developed EuGlide system.

Timeline

Start
2023-11-30
Primary completion
2025-04
Completion
2025-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramlintide Peptide
Background Lyumjev Unknown