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Completed Phase 3 Interventional Results available

Efficacy and Safety of Semaglutide Once-weekly Versus Placebo as add-on to SGLT-2i in Subjects With Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT03086330

Public ClinicalTrials.gov record NCT03086330. 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 2, 2026, 3:51 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 Semaglutide Once-weekly Versus Placebo as add-on to SGLT-2i in Subjects With Type 2 Diabetes Mellitus. A 30-week Randomised, Double-blind, Placebo-controlled Trial

Brief summary

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

This trial is conducted in Asia, Europe and North America. The aim of the trial is to compare the effect of semaglutide s.c. 1.0 mg once-weekly versus placebo as add-on to sodium glucose co-transporter-2 inhibitor (SGLT-2i) monotherapy or in combination with either metformin or sulfonylurea on glycaemic control after 30 weeks of treatment in subjects with type 2 diabetes. Subjects will remain on their pre-trial medication.

Study identification

NCT ID
NCT03086330
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
302 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
Mar 14, 2017
Primary completion
Jul 3, 2018
Completion
Aug 5, 2018
Last update posted
Jul 1, 2021

2017 – 2018

United States locations

U.S. sites
43
U.S. states
19
U.S. cities
41
Facility City State ZIP Site status
Novo Nordisk Investigational Site Andalusia Alabama 36420
Novo Nordisk Investigational Site Anniston Alabama 36207
Novo Nordisk Investigational Site Glendale Arizona 85308
Novo Nordisk Investigational Site Phoenix Arizona 85037
Novo Nordisk Investigational Site Tempe Arizona 85283
Novo Nordisk Investigational Site Little Rock Arkansas 72211
Novo Nordisk Investigational Site La Jolla California 92037
Novo Nordisk Investigational Site Lincoln California 95648
Novo Nordisk Investigational Site Northridge California 91325
Novo Nordisk Investigational Site Edgewater Florida 32132
Novo Nordisk Investigational Site Maitland Florida 32751-4422
Novo Nordisk Investigational Site Lawrenceville Georgia 30046
Novo Nordisk Investigational Site Woodstock Georgia 30189-4255
Novo Nordisk Investigational Site Hutchinson Kansas 67502-1131
Novo Nordisk Investigational Site Lexington Kentucky 40503
Novo Nordisk Investigational Site Baltimore Maryland 21204
Novo Nordisk Investigational Site Troy Michigan 48098
Novo Nordisk Investigational Site Jefferson City Missouri 65109
Novo Nordisk Investigational Site Albany New York 12206
Novo Nordisk Investigational Site Smithtown New York 11787
Novo Nordisk Investigational Site West Seneca New York 14224
Novo Nordisk Investigational Site Charlotte North Carolina 28207
Novo Nordisk Investigational Site Charlotte North Carolina 28226
Novo Nordisk Investigational Site Gastonia North Carolina 28054
Novo Nordisk Investigational Site Greenville North Carolina 27834
Novo Nordisk Investigational Site Kinston North Carolina 28501
Novo Nordisk Investigational Site Morehead City North Carolina 28557-4346
Novo Nordisk Investigational Site Norman Oklahoma 73069
Novo Nordisk Investigational Site Beaver Pennsylvania 15009
Novo Nordisk Investigational Site McMurray Pennsylvania 15317
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15243
Novo Nordisk Investigational Site Arlington Texas 76012-4637
Novo Nordisk Investigational Site Austin Texas 78745
Novo Nordisk Investigational Site Dallas Texas 75208
Novo Nordisk Investigational Site Dallas Texas 75231
Novo Nordisk Investigational Site Houston Texas 77081
Novo Nordisk Investigational Site Irving Texas 75061-2210
Novo Nordisk Investigational Site Shavano Park Texas 78231
Novo Nordisk Investigational Site Sugar Land Texas 77479
Novo Nordisk Investigational Site Victoria Texas 77901
Novo Nordisk Investigational Site Murray Utah 84123
Novo Nordisk Investigational Site Chesapeake Virginia 23321
Novo Nordisk Investigational Site Olympia Washington 98502

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 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03086330, 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 1, 2021 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03086330 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →