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Completed Phase 3 Interventional Results available

Efficacy and Safety of Insulin Degludec/Insulin Aspart in Insulin-naïve Subjects With Type 2 Diabetes Using Two Dosing Regimens

ClinicalTrials.gov ID: NCT01365507

Public ClinicalTrials.gov record NCT01365507. 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, 9:11 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 the Efficacy and Safety of Insulin Degludec/Insulin Aspart Once Daily in Insulin-naïve Subjects With Type 2 Diabetes Mellitus When Using Two Different Titration Algorithms (BOOST™: SIMPLE USE)

Study identification

NCT ID
NCT01365507
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
276 participants

Conditions and interventions

Interventions

  • insulin degludec/insulin aspart 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
May 31, 2011
Primary completion
Mar 31, 2012
Completion
Mar 31, 2012
Last update posted
Mar 16, 2017

2011 – 2012

United States locations

U.S. sites
25
U.S. states
11
U.S. cities
23
Facility City State ZIP Site status
Novo Nordisk Investigational Site Concord California 94520-1926
Novo Nordisk Investigational Site Los Angeles California 90057
Novo Nordisk Investigational Site Montclair California 91763
Novo Nordisk Investigational Site Palm Springs California 92262
Novo Nordisk Investigational Site Spring Valley California 91978
Novo Nordisk Investigational Site Jacksonville Florida 32209-6511
Novo Nordisk Investigational Site Jacksonville Florida 32258
Novo Nordisk Investigational Site Pembroke Pines Florida 33027
Novo Nordisk Investigational Site Crestview Hills Kentucky 41017-3464
Novo Nordisk Investigational Site Madisonville Kentucky 42431
Novo Nordisk Investigational Site Paducah Kentucky 42003
Novo Nordisk Investigational Site Hyattsville Maryland 20782
Novo Nordisk Investigational Site North East Maryland 21901
Novo Nordisk Investigational Site Detroit Michigan 48235
Novo Nordisk Investigational Site Troy Michigan 48085-5524
Novo Nordisk Investigational Site Eagan Minnesota 55123
Novo Nordisk Investigational Site Smithtown New York 11787
Novo Nordisk Investigational Site Asheboro North Carolina 27203
Novo Nordisk Investigational Site Dallas Texas 75230
Novo Nordisk Investigational Site Dallas Texas 75246
Novo Nordisk Investigational Site Houston Texas 77070
Novo Nordisk Investigational Site Lubbock Texas 79423
Novo Nordisk Investigational Site Sugar Land Texas 77478
Novo Nordisk Investigational Site Newport News Virginia 23606
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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01365507, 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 Mar 16, 2017 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01365507 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →