CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 582 enrolled
Drug / intervention
insulin icodec +2 moredrug
Likely dose
insulin icodec 700 unitsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04848480
NCT04848480Phase 3Completed

Efficacy and Safety of Once Weekly Insulin Icodec Compared to Once Daily Insulin Degludec 100 Units/mL, Both in Combination With Insulin Aspart, in Adults With Type 1 Diabetes. A 26-week, Randomised, Multicentre, Open-label, Active-controlled, Parallel Group, Two Armed, Treat-to-target Trial Investigating the Effect on Glycaemic Control and Safety of Treatment With Once Weekly Insulin Icodec Compared to Once Daily Insulin Degludec, Both in Combination With Insulin Aspart in Adults With Type 1 Diabetes, With a 26-week Extension Investigating Long Term Safety

Novo Nordisk A/S·interventional·Posted Apr 19, 2021·Updated Dec 4, 2025

In Brief

A Phase 3 clinical trial evaluating insulin icodec, insulin degludec, and 1 other intervention for Diabetes Mellitus, Type 1. Completed, enrolled 582 participants across 130 sites in 12 countries.

Detailed Summary

This study compares insulin icodec (a new insulin) to insulin degludec (an insulin already available on the market) in people with type 1 diabetes. The study will look at how well insulin icodec taken weekly controls blood sugar compared to insulin degludec taken daily. Participants will either get insulin icodec that participants will have to inject once a week on the same day of the week, or insulin degludec that participants will have to inject once a day at the same time every day. Which treatment participants get is decided at random. Participants will also get a mealtime insulin. The insulin is injected with a needle in a skin fold in the thigh, upper arm or stomach. The study will last for about 1 year and 2 months. Participants will have 28 clinic visits and 28 phone calls with the study doctor. At 11 clinic visits participants will have blood samples taken. At 6 clinic visits participants cannot eat or drink (except for water) for 8 hours before the visit. Participants will be asked to wear a sensor that measures your blood sugar all the time. Participants will be asked to wear it for a total of 57 weeks (around 1 year). Women cannot take part if pregnant, breast-feeding or plan to become pregnant during the study period.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustria, Canada, Germany, India, Italy, Japan, Netherlands, Russia, Spain, Turkey (Türkiye), United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20222023202420252026
First PostedApr 19, 2021
Enrollment StartApr 30, 2021
Primary CompletionApr 28, 2022
Study CompletionDec 2, 2022
TodayJul 2, 2026
Enrollment to primary: 12 monthsPosted 5.2 years ago

Interventions

insulin icodecdrug

insulin icodec 700 units/mL, subcutaneously (under the skin), solution for injection once weekly

insulin degludecdrug

insulin degludec 100 units/mL, subcutaneously (under the skin), solution for injection once daily

insulin aspartdrug

insulin aspart 100 units/mL, subcutaneously (under the skin), solution for injection daily