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Completed Phase 3 Interventional Results available

A Trial Comparing Efficacy and Safety of Insulin Degludec and Insulin Glargine in Insulin naïve Subjects With Type 2 Diabetes

ClinicalTrials.gov ID: NCT01849289

Public ClinicalTrials.gov record NCT01849289. 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 May 11, 2026, 9:13 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 Trial Comparing Efficacy and Safety of Insulin Degludec and Insulin Glargine in Insulin naïve Subjects With Type 2 Diabetes (BEGIN™: ONCE)

Study identification

NCT ID
NCT01849289
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
833 participants

Conditions and interventions

Interventions

  • Insulin Degludec Drug
  • Insulin Glargine Drug

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
Jun 1, 2013
Primary completion
May 14, 2014
Completion
May 14, 2014
Last update posted
Apr 6, 2017

2013 – 2014

United States locations

U.S. sites
18
U.S. states
16
U.S. cities
18
Facility City State ZIP Site status
Novo Nordisk Investigational Site Anaheim California 92801
Novo Nordisk Investigational Site Lomita California 90717
Novo Nordisk Investigational Site Los Angeles California 90057
Novo Nordisk Investigational Site Golden Colorado 80401
Novo Nordisk Investigational Site Clearwater Florida 33765
Novo Nordisk Investigational Site Chicago Illinois 60607
Novo Nordisk Investigational Site Crestview Hills Kentucky 41017-3464
Novo Nordisk Investigational Site Metairie Louisiana 70002
Novo Nordisk Investigational Site Troy Michigan 48098
Novo Nordisk Investigational Site Chesterfield Missouri 63017
Novo Nordisk Investigational Site Nashua New Hampshire 03063
Novo Nordisk Investigational Site Toms River New Jersey 08755-8050
Novo Nordisk Investigational Site Smithtown New York 11787
Novo Nordisk Investigational Site Simpsonville South Carolina 29681
Novo Nordisk Investigational Site Jackson Tennessee 38305
Novo Nordisk Investigational Site Dallas Texas 75230
Novo Nordisk Investigational Site Newport News Virginia 23606
Novo Nordisk Investigational Site Kenosha Wisconsin 53142

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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01849289, 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 6, 2017 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01849289 live on ClinicalTrials.gov.

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