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Completed Phase 3 Interventional Results available

Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation Versus Sitagliptin in Subjects With Type 2 Diabetes Mellitus.

ClinicalTrials.gov ID: NCT02849080

Public ClinicalTrials.gov record NCT02849080. 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 29, 2026, 2:09 AM EDT

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

Official title

Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation Versus Sitagliptin in Subjects With Type 2 Diabetes Mellitus

Brief summary

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

This trial is globally conducted. The aim of this trial is to investigate Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation versus Sitagliptin in Subjects with Type 2 Diabetes Mellitus.

Study identification

NCT ID
NCT02849080
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
504 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
Sep 19, 2016
Primary completion
Feb 27, 2018
Completion
Mar 26, 2019
Last update posted
Jul 19, 2022

2016 – 2019

United States locations

U.S. sites
37
U.S. states
22
U.S. cities
36
Facility City State ZIP Site status
Novo Nordisk Investigational Site Glendale Arizona 85306-4652 —
Novo Nordisk Investigational Site Phoenix Arizona 85050 —
Novo Nordisk Investigational Site Lancaster California 93534 —
Novo Nordisk Investigational Site West Hills California 91304 —
Novo Nordisk Investigational Site Boynton Beach Florida 33472 —
Novo Nordisk Investigational Site Lake Worth Florida 33461 —
Novo Nordisk Investigational Site Miami Lakes Florida 33014 —
Novo Nordisk Investigational Site Port Orange Florida 32127 —
Novo Nordisk Investigational Site Tampa Florida 33607 —
Novo Nordisk Investigational Site Tampa Florida 33614 —
Novo Nordisk Investigational Site Atlanta Georgia 30318 —
Novo Nordisk Investigational Site Blackfoot Idaho 83221 —
Novo Nordisk Investigational Site Evanston Illinois 60201-2477 —
Novo Nordisk Investigational Site Greenfield Indiana 46140 —
Novo Nordisk Investigational Site Muncie Indiana 47304 —
Novo Nordisk Investigational Site Louisville Kentucky 40213 —
Novo Nordisk Investigational Site Metairie Louisiana 70002 —
Novo Nordisk Investigational Site Oxon Hill Maryland 20745 —
Novo Nordisk Investigational Site Flint Michigan 48504 —
Novo Nordisk Investigational Site Billings Montana 59101 —
Novo Nordisk Investigational Site Henderson Nevada 89052-2649 —
Novo Nordisk Investigational Site Albuquerque New Mexico 87109-2134 —
Novo Nordisk Investigational Site Chapel Hill North Carolina 27514 —
Novo Nordisk Investigational Site Greensboro North Carolina 27408 —
Novo Nordisk Investigational Site Greenville North Carolina 27834 —
Novo Nordisk Investigational Site Whiteville North Carolina 28472 —
Novo Nordisk Investigational Site Cleveland Ohio 44122 —
Novo Nordisk Investigational Site Mentor Ohio 44060 —
Novo Nordisk Investigational Site Wadsworth Ohio 44281 —
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15236 —
Novo Nordisk Investigational Site Murrells Inlet South Carolina 29576 —
Novo Nordisk Investigational Site Myrtle Beach South Carolina 29572 —
Novo Nordisk Investigational Site Kingsport Tennessee 37660 —
Novo Nordisk Investigational Site Corpus Christi Texas 78413 —
Novo Nordisk Investigational Site Dallas Texas 75231 —
Novo Nordisk Investigational Site Chesapeake Virginia 23321 —
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 46 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02849080, 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 Jul 19, 2022 · Synced Sep 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02849080 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →