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Completed Phase 3 Interventional Results available

Comparison of NN1250 Versus Insulin Glargine in Subjects With Type 2 Diabetes

ClinicalTrials.gov ID: NCT00982644

Public ClinicalTrials.gov record NCT00982644. 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 24, 2026, 3:27 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

NN1250-3579: A 52-week Randomised, Controlled, Open Label, Multicentre, Multinational Treat-to-target Trial Comparing the Efficacy and Safety of SIBA and Insulin Glargine, Both Injected Once Daily in Combination With Oral Anti-diabetic Drugs (OAD), in Subjects With Type 2 Diabetes Mellitus Currently Treated With OAD(s) and Qualifying for More Intensified Treatment / NN1250-3643: An Extension Trial to NN1250-3579 Comparing Safety and Efficacy of NN1250 Plus OAD(s) With Insulin Glargine Plus OAD(s) in Type 2 Diabetes (BEGIN™: Once Long)

Brief summary

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

This trial is conducted in Europe and the United States of America (USA). The aim of this trial is to compare NN1250 (insulin degludec (IDeg)) with insulin glargine (IGlar) in subjects with type 2 diabetes never treated with insulin followed by the extension trial investigating the long-term safety and tolerability in terms of comparing NN1250 with insulin glargine in subjects with type 2 diabetes. All oral anti-diabetic drug (OAD) treatment will be discontinued when trial participant enters the main trial (NN1250-3579) with the exception of metformin and dipeptidyl peptidase-IV (DPP-IV) inhibitor treatment (only in countries where DPP-IV inhibitor treatment is approved for combination treatment together with insulin, otherwise DPP-IV inhibitor treatment is also discontinued). Subjects who consent to participate in the extension trial will continue the treatment (NN1250 or insulin glargine + oral antidiabetic drugs (OADs)) to which they were randomly allocated in the 52 week main trial. The main period is registered internally at Novo Nordisk as NN1250-3579 while the extension period is registered as NN1250-3643.

Study identification

NCT ID
NCT00982644
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
1,030 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
Aug 31, 2009
Primary completion
Nov 30, 2010
Completion
Nov 30, 2010
Last update posted
Feb 8, 2017

2009 – 2010

United States locations

U.S. sites
86
U.S. states
28
U.S. cities
83
Facility City State ZIP Site status
Novo Nordisk Investigational Site Bay Minette Alabama 36507-4198 —
Novo Nordisk Investigational Site Birmingham Alabama 35209 —
Novo Nordisk Investigational Site Huntsville Alabama 35801 —
Novo Nordisk Investigational Site Goodyear Arizona 85395 —
Novo Nordisk Investigational Site Anaheim California 92801 —
Novo Nordisk Investigational Site Concord California 94520-1926 —
Novo Nordisk Investigational Site La Jolla California 92037 —
Novo Nordisk Investigational Site Lancaster California 93534 —
Novo Nordisk Investigational Site Long Beach California 90806 —
Novo Nordisk Investigational Site Los Angeles California 90057 —
Novo Nordisk Investigational Site Mission Hills California 91345 —
Novo Nordisk Investigational Site National City California 91950 —
Novo Nordisk Investigational Site North Hollywood California 91606 —
Novo Nordisk Investigational Site Northridge California 91325 —
Novo Nordisk Investigational Site Palm Springs California 92262 —
Novo Nordisk Investigational Site San Mateo California 94401 —
Novo Nordisk Investigational Site Santa Monica California 90404 —
Novo Nordisk Investigational Site Spring Valley California 91978 —
Novo Nordisk Investigational Site Tarzana California 91356-3551 —
Novo Nordisk Investigational Site Tustin California 92780 —
Novo Nordisk Investigational Site Norwalk Connecticut 06851 —
Novo Nordisk Investigational Site Boynton Beach Florida 33472 —
Novo Nordisk Investigational Site Jacksonville Florida 32208 —
Novo Nordisk Investigational Site Melbourne Florida 32901 —
Novo Nordisk Investigational Site Miami Florida 33156 —
Novo Nordisk Investigational Site Miami Florida 33169 —
Novo Nordisk Investigational Site New Port Richey Florida 34652 —
Novo Nordisk Investigational Site Orange Park Florida 32073 —
Novo Nordisk Investigational Site Orlando Florida 32806 —
Novo Nordisk Investigational Site Palm Harbor Florida 34684 —
Novo Nordisk Investigational Site West Palm Beach Florida 33401 —
Novo Nordisk Investigational Site Decatur Georgia 30033 —
Novo Nordisk Investigational Site Fort Valley Georgia 31030-5008 —
Novo Nordisk Investigational Site Idaho Falls Idaho 83404-7596 —
Novo Nordisk Investigational Site Chicago Illinois 60607 —
Novo Nordisk Investigational Site Evansville Indiana 47714 —
Novo Nordisk Investigational Site Indianapolis Indiana 46217 —
Novo Nordisk Investigational Site Lexington Kentucky 40503 —
Novo Nordisk Investigational Site Paducah Kentucky 42003 —
Novo Nordisk Investigational Site Metairie Louisiana 70002 —
Novo Nordisk Investigational Site Slidell Louisiana 70461-4231 —
Novo Nordisk Investigational Site Greenbelt Maryland 20770 —
Novo Nordisk Investigational Site North East Maryland 21901 —
Novo Nordisk Investigational Site Reisterstown Maryland 21136-2516 —
Novo Nordisk Investigational Site Rockville Maryland 20852 —
Novo Nordisk Investigational Site Brockton Massachusetts 02301 —
Novo Nordisk Investigational Site North Dartmouth Massachusetts 02747 —
Novo Nordisk Investigational Site St Louis Missouri 63104 —
Novo Nordisk Investigational Site St Louis Missouri 63141 —
Novo Nordisk Investigational Site Henderson Nevada 89052-2649 —
Novo Nordisk Investigational Site Las Vegas Nevada 89117 —
Novo Nordisk Investigational Site Toms River New Jersey 08755-8050 —
Novo Nordisk Investigational Site Northport New York 11768 —
Novo Nordisk Investigational Site Staten Island New York 10301 —
Novo Nordisk Investigational Site Asheboro North Carolina 27203 —
Novo Nordisk Investigational Site Charlotte North Carolina 28209 —
Novo Nordisk Investigational Site Cincinnati Ohio 45255 —
Novo Nordisk Investigational Site Dayton Ohio 45406 —
Novo Nordisk Investigational Site Toledo Ohio 43606-2920 —
Novo Nordisk Investigational Site Oklahoma City Oklahoma 73103 —
Novo Nordisk Investigational Site Kingston Pennsylvania 18704 —
Novo Nordisk Investigational Site Langhorne Pennsylvania 19047 —
Novo Nordisk Investigational Site Melrose Park Pennsylvania 19027 —
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15241 —
Novo Nordisk Investigational Site West Reading Pennsylvania 19611 —
Novo Nordisk Investigational Site East Providence Rhode Island 02914 —
Novo Nordisk Investigational Site Columbia South Carolina 29203 —
Novo Nordisk Investigational Site Greer South Carolina 29651 —
Novo Nordisk Investigational Site Newberry South Carolina 29108-2249 —
Novo Nordisk Investigational Site Chattanooga Tennessee 37411 —
Novo Nordisk Investigational Site Harriman Tennessee 37748-8653 —
Novo Nordisk Investigational Site Humboldt Tennessee 38343 —
Novo Nordisk Investigational Site Nashville Tennessee 37203 —
Novo Nordisk Investigational Site Arlington Texas 76014 —
Novo Nordisk Investigational Site Corpus Christi Texas 78404 —
Novo Nordisk Investigational Site Dallas Texas 75230 —
Novo Nordisk Investigational Site Dallas Texas 75246 —
Novo Nordisk Investigational Site El Paso Texas 79912 —
Novo Nordisk Investigational Site Hurst Texas 76054 —
Novo Nordisk Investigational Site Irving Texas 75061-2210 —
Novo Nordisk Investigational Site Lubbock Texas 79423 —
Novo Nordisk Investigational Site San Antonio Texas 78215 —
Novo Nordisk Investigational Site Sugar Land Texas 77479 —
Novo Nordisk Investigational Site Richmond Virginia 23233 —
Novo Nordisk Investigational Site Spokane Washington 99218 —
Novo Nordisk Investigational Site Milwaukee Wisconsin 53209 —

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 101 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00982644, 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 Feb 8, 2017 · Synced Sep 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00982644 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →