Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Study Using Flash Glucose Measurements for a New Once-weekly Insulin (Insulin Icodec) in People With Type 2 Diabetes Who Have Not Used Insulin Before (ONWARDS 9)

ClinicalTrials.gov ID: NCT05823948

Public ClinicalTrials.gov record NCT05823948. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 11:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study to Evaluate Flash Glucose Monitoring Based Titration of Once-weekly Insulin Icodec in Insulin-naïve Participants With Type 2 Diabetes

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study looks at how a person with type 2 diabetes can be treated with insulin icodec and a flash glucose monitor (a small sensor inserted under the skin to measure blood sugar all the time). The study will look at how well insulin icodec controls blood sugar when used in combination with a flash glucose monitor. Participants will get insulin icodec that they have to inject once a week on the same day of the week. The insulin will be injected with a needle in a skin fold in the thigh, upper arm, or stomach. The study will last for about 8 months. Participants will have to wear a flash glucose monitor throughout the study. This is a sensor that fits on arm. Participants will be asked to use a commercially available app called LibreView to allow team to view flash glucose monitor data. Participants will get a study phone to scan the flash glucose monitor 4 times daily and they will be able to see all of the flash glucose monitor data during the study. Women cannot take part if pregnant, breast-feeding or planning to get pregnant during the study period.

Study identification

NCT ID
NCT05823948
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
51 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 10, 2023
Primary completion
Mar 5, 2024
Completion
Apr 10, 2024
Last update posted
Apr 29, 2026

2023 – 2024

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Desert Oasis Hlthcr Med Group Palm Springs California 92262
Clinical Trials Research_Sacramento_0 Sacramento California 95821
San Diego Family Care San Diego California 92111
Mills-Peninsula Hlth Services San Mateo California 94401
Florida Inst For Clin Res LLC Orlando Florida 32825
Metabolic Research Institute Inc West Palm Beach Florida 33401
East West Med Res Inst Honolulu Hawaii 96814
Northern Pines Hlth Ctr, PC Buckley Michigan 49620
International Diabetes Center Minneapolis Minnesota 55416
Palm Research Center Inc-Vegas Las Vegas Nevada 89148
Accellacare_NC Wilmington North Carolina 28401
Diabetes & Endocrinology Asso Canton Ohio 44718
AM Diabetes And Endocrinology Bartlett Tennessee 38133
Amarillo Medical Specialists Amarillo Texas 79124
Velocity Clin Res, Dallas Dallas Texas 75230
UT Southwestern Med Cntr Dallas Texas 75390-9302
Fmc Science, Llc Lampasas Texas 76550
Clinical Trials of Texas Inc San Antonio Texas 78229
Northeast Clinical Research of San Antonio San Antonio Texas 78233
Chrysalis Clinical Research St. George Utah 84790

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05823948, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 29, 2026 · Synced Sep 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05823948 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →