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Completed Phase 2 Interventional Results available

A Research Study to Compare Insulin 287 Once a Week to Insulin Glargine (100 Units/mL) Once a Day in People With Type 2 Diabetes.

ClinicalTrials.gov ID: NCT03751657

Public ClinicalTrials.gov record NCT03751657. 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 Jul 23, 2026, 2:59 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

An Investigational Trial Comparing the Efficacy and Safety of Once Weekly NNC0148-0287 C (Insulin 287) Versus Once Daily Insulin Glargine, Both in Combination With Metformin, With or Without DPP-4 Inhibitors, in Insulin naïve Subjects With Type 2 Diabetes Mellitus

Study identification

NCT ID
NCT03751657
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
247 participants

Conditions and interventions

Interventions

  • Insulin icodec Drug
  • Placebo (insulin 287) Drug
  • Metformin Drug
  • Dipeptidyl peptidase-4 inhibitors Drug
  • Insulin glargine Drug
  • Placebo (insulin glargine) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Nov 28, 2018
Primary completion
Dec 15, 2019
Completion
Jan 16, 2020
Last update posted
Apr 1, 2021

2018 – 2020

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
Novo Nordisk Investigational Site Lancaster California 93534
Novo Nordisk Investigational Site Ventura California 93003
Novo Nordisk Investigational Site Walnut Creek California 94598
Novo Nordisk Investigational Site Roswell Georgia 30076
Novo Nordisk Investigational Site Lexington Kentucky 40503
Novo Nordisk Investigational Site Las Vegas Nevada 89128
Novo Nordisk Investigational Site Charlotte North Carolina 28277
Novo Nordisk Investigational Site Whiteville North Carolina 28472
Novo Nordisk Investigational Site Chattanooga Tennessee 37404
Novo Nordisk Investigational Site Chattanooga Tennessee 37411
Novo Nordisk Investigational Site Austin Texas 78731
Novo Nordisk Investigational Site Dallas Texas 75230
Novo Nordisk Investigational Site Dallas Texas 75390-9302
Novo Nordisk Investigational Site Renton Washington 98057

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 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03751657, 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 1, 2021 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03751657 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →