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Completed Phase 2 Interventional Results available

Investigation of Safety and Efficacy of Once-daily Semaglutide in Obese Subjects Without Diabetes Mellitus

ClinicalTrials.gov ID: NCT02453711

Public ClinicalTrials.gov record NCT02453711. 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 Jun 25, 2026, 10:44 PM 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
NCT02453711
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
957 participants

Conditions and interventions

Interventions

  • semaglutide Drug
  • liraglutide 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
Sep 30, 2015
Primary completion
Mar 29, 2017
Completion
Apr 11, 2017
Last update posted
Apr 16, 2020

2015 – 2017

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Novo Nordisk Investigational Site Anaheim California 92801
Novo Nordisk Investigational Site San Diego California 92108
Novo Nordisk Investigational Site Golden Colorado 80401
Novo Nordisk Investigational Site Waterbury Connecticut 06708
Novo Nordisk Investigational Site Washington D.C. District of Columbia 20011
Novo Nordisk Investigational Site Crystal River Florida 34429
Novo Nordisk Investigational Site Jacksonville Florida 32205
Novo Nordisk Investigational Site Jacksonville Florida 32216
Novo Nordisk Investigational Site Plantation Florida 33324
Novo Nordisk Investigational Site Elkridge Maryland 21075-6437
Novo Nordisk Investigational Site Rochester New York 14609
Novo Nordisk Investigational Site Cincinnati Ohio 45219
Novo Nordisk Investigational Site Wadsworth Ohio 44281
Novo Nordisk Investigational Site Portland Oregon 97239
Novo Nordisk Investigational Site Charleston South Carolina 29425
Novo Nordisk Investigational Site Greer South Carolina 29651
Novo Nordisk Investigational Site Bristol Tennessee 37620-7352
Novo Nordisk Investigational Site Dallas Texas 75251
Novo Nordisk Investigational Site Round Rock Texas 78681
Novo Nordisk Investigational Site Sugar Land Texas 77479
Novo Nordisk Investigational Site Arlington Virginia 22206
Novo Nordisk Investigational Site Richmond Virginia 23294

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 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02453711, 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 16, 2020 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02453711 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →