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Completed Phase 3 Interventional Results available

A 38 Week Trial Comparing Effect and Safety of Insulin Degludec/Insulin Aspart vs. Insulin Glargine Plus Insulin Aspart in Subjects With Type 2 Diabetes Treated With Basal Insulin With or Without Oral Antidiabetic Treatment in Need of Treatment Intensification

ClinicalTrials.gov ID: NCT02906917

Public ClinicalTrials.gov record NCT02906917. 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 Nov 5, 2026, 10:11 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

This Trial is Conducted Globally. The Aim of This Trial is to Compare the Effect and Safety of Insulin Degludec/Insulin Aspart vs. Insulin Glargine Plus Insulin Aspart in Subjects With Type 2 Diabetes Treated With Basal Insulin With or Without Oral Antidiabetic Treatment in Need of Treatment Intensification.

Brief summary

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

Trial comparing effect and safety of insulin degludec/insulin aspart vs. insulin glargine plus insulin aspart in subjects with type 2 diabetes treated with basal insulin with or without oral antidiabetic treatment in need of treatment intensification.

Study identification

NCT ID
NCT02906917
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
532 participants

Conditions and interventions

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
Sep 20, 2016 (Actual)
Primary completion
Aug 31, 2017 (Actual)
Completion
Dec 24, 2017 (Actual)
Last update posted
Nov 13, 2019

2016 – 2017

United States locations

U.S. sites
30
U.S. states
13
U.S. cities
29
Facility City State ZIP Site status
Novo Nordisk Investigational Site Glendale Arizona 85306-4652 —
Novo Nordisk Investigational Site Phoenix Arizona 85050 —
Novo Nordisk Investigational Site Anaheim California 92801 —
Novo Nordisk Investigational Site Concord California 94520 —
Novo Nordisk Investigational Site Fresno California 93720 —
Novo Nordisk Investigational Site La Jolla California 92037 —
Novo Nordisk Investigational Site Northridge California 91325 —
Novo Nordisk Investigational Site Danbury Connecticut 06810 —
Novo Nordisk Investigational Site Fort Lauderdale Florida 33312 —
Novo Nordisk Investigational Site Fort Lauderdale Florida 33316 —
Novo Nordisk Investigational Site Jacksonville Florida 32205 —
Novo Nordisk Investigational Site Kissimmee Florida 34744 —
Novo Nordisk Investigational Site Roswell Georgia 30076 —
Novo Nordisk Investigational Site Louisville Kentucky 40213 —
Novo Nordisk Investigational Site Chesterfield Missouri 63017 —
Novo Nordisk Investigational Site New York New York 10029 —
Novo Nordisk Investigational Site Westfield New York 14787 —
Novo Nordisk Investigational Site Wilmington North Carolina 28401 —
Novo Nordisk Investigational Site Franklin Ohio 45005 —
Novo Nordisk Investigational Site Bartlett Tennessee 38133 —
Novo Nordisk Investigational Site Chattanooga Tennessee 37411 —
Novo Nordisk Investigational Site Kingsport Tennessee 37660 —
Novo Nordisk Investigational Site Knoxville Tennessee 37938 —
Novo Nordisk Investigational Site Nashville Tennessee 37228 —
Novo Nordisk Investigational Site Austin Texas 78758 —
Novo Nordisk Investigational Site Dallas Texas 75390-9302 —
Novo Nordisk Investigational Site San Antonio Texas 78230 —
Novo Nordisk Investigational Site Chesapeake Virginia 23321 —
Novo Nordisk Investigational Site Midlothian Virginia 23114 —
Novo Nordisk Investigational Site Winchester Virginia 22601-3834 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02906917, 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 Nov 13, 2019 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02906917 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →