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Completed Phase 3 Interventional Results available

Effect and Safety of Liraglutide 3.0 mg in Subjects With Overweight or Obesity and Type 2 Diabetes Mellitus Treated With Basal Insulin

ClinicalTrials.gov ID: NCT02963922

Public ClinicalTrials.gov record NCT02963922. 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 12, 2026, 4:40 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT02963922
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
396 participants

Conditions and interventions

Interventions

  • Liraglutide 3.0 mg Drug
  • Placebo 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
Feb 5, 2017
Primary completion
Sep 9, 2018
Completion
Sep 24, 2018
Last update posted
Mar 29, 2020

2017 – 2018

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Novo Nordisk Investigational Site Birmingham Alabama 35294
Novo Nordisk Investigational Site Concord California 94520
Novo Nordisk Investigational Site Fresno California 93720
Novo Nordisk Investigational Site Jacksonville Florida 32205
Novo Nordisk Investigational Site Plantation Florida 33324
Novo Nordisk Investigational Site Roswell Georgia 30076
Novo Nordisk Investigational Site Honolulu Hawaii 96814
Novo Nordisk Investigational Site Chicago Illinois 60607
Novo Nordisk Investigational Site Louisville Kentucky 40213
Novo Nordisk Investigational Site North Dartmouth Massachusetts 02747
Novo Nordisk Investigational Site Minneapolis Minnesota 55416
Novo Nordisk Investigational Site Butte Montana 59701
Novo Nordisk Investigational Site Albany New York 12206
Novo Nordisk Investigational Site Wilmington North Carolina 28401
Novo Nordisk Investigational Site Austin Texas 78731
Novo Nordisk Investigational Site Austin Texas 78749
Novo Nordisk Investigational Site Dallas Texas 75230
Novo Nordisk Investigational Site Dallas Texas 75231
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 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02963922, 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 29, 2020 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02963922 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →