Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Research Study to Compare Two Doses of Semaglutide Taken Once Weekly in People With Type 2 Diabetes

ClinicalTrials.gov ID: NCT03989232

Public ClinicalTrials.gov record NCT03989232. 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 Oct 7, 2026, 9:03 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 2.0 mg s.c. Once-weekly Compared to Semaglutide 1.0 mg s.c. Once-weekly in Subjects With Type 2 Diabetes

Brief summary

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

This study compares the effect of two doses of semaglutide (1.0 mg and 2.0 mg) in people with type 2 diabetes (T2D). People taking part in the study will take the medicine together with their current diabetes medicine (sulphonylurea and/or metformin). Participants will get a dose of either 1.0 mg or 2.0 mg semaglutide once a week - which dose is decided by chance. Participants will inject semaglutide under the skin once a week. The study will last for about 49 weeks. Participants will have 9 clinic visits and 2 phone calls with the study doctor. At the visits participants will have blood taken and eye tests done. Women cannot take part if pregnant, breast-feeding or planning to become pregnant during the study period. Female participants who can get pregnant will be checked 11 times for pregnancy via urine tests.

Study identification

NCT ID
NCT03989232
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
961 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
Jun 19, 2019 (Actual)
Primary completion
Sep 18, 2020 (Actual)
Completion
Nov 9, 2020 (Actual)
Last update posted
Feb 13, 2023

2019 – 2020

United States locations

U.S. sites
61
U.S. states
24
U.S. cities
58
Facility City State ZIP Site status
Novo Nordisk Investigational Site Birmingham Alabama 35205 —
Novo Nordisk Investigational Site Chandler Arizona 85224 —
Novo Nordisk Investigational Site Glendale Arizona 85306 —
Novo Nordisk Investigational Site Glendale Arizona 85308 —
Novo Nordisk Investigational Site Mesa Arizona 85213 —
Novo Nordisk Investigational Site Phoenix Arizona 85050 —
Novo Nordisk Investigational Site Buena Park California 90620 —
Novo Nordisk Investigational Site Fresno California 93720 —
Novo Nordisk Investigational Site Los Angeles California 90057 —
Novo Nordisk Investigational Site San Diego California 92103 —
Novo Nordisk Investigational Site Spring Valley California 91978 —
Novo Nordisk Investigational Site Walnut Creek California 94598 —
Novo Nordisk Investigational Site West Hills California 91304 —
Novo Nordisk Investigational Site Colorado Springs Colorado 80906 —
Novo Nordisk Investigational Site Coral Gables Florida 33134 —
Novo Nordisk Investigational Site Hollywood Florida 33024 —
Novo Nordisk Investigational Site Jacksonville Florida 32216 —
Novo Nordisk Investigational Site Adairsville Georgia 30103 —
Novo Nordisk Investigational Site Alpharetta Georgia 30022 —
Novo Nordisk Investigational Site Roswell Georgia 30076 —
Novo Nordisk Investigational Site Meridian Idaho 83646 —
Novo Nordisk Investigational Site Carlinville Illinois 62626 —
Novo Nordisk Investigational Site Chicago Illinois 60607 —
Novo Nordisk Investigational Site Peoria Illinois 61603 —
Novo Nordisk Investigational Site Topeka Kansas 66606 —
Novo Nordisk Investigational Site Lexington Kentucky 40503 —
Novo Nordisk Investigational Site Louisville Kentucky 40213 —
Novo Nordisk Investigational Site Lake Charles Louisiana 70601 —
Novo Nordisk Investigational Site Sterling Heights Michigan 48310-3503 —
Novo Nordisk Investigational Site Jefferson City Missouri 65109 —
Novo Nordisk Investigational Site Butte Montana 59701 —
Novo Nordisk Investigational Site Trenton New Jersey 08611 —
Novo Nordisk Investigational Site New Windsor New York 12553 —
Novo Nordisk Investigational Site Chapel Hill North Carolina 27514 —
Novo Nordisk Investigational Site Greensboro North Carolina 27408 —
Novo Nordisk Investigational Site Salisbury North Carolina 28144 —
Novo Nordisk Investigational Site Statesville North Carolina 28625 —
Novo Nordisk Investigational Site Wilmington North Carolina 28401 —
Novo Nordisk Investigational Site Columbus Ohio 43213 —
Novo Nordisk Investigational Site Mason Ohio 45040-6815 —
Novo Nordisk Investigational Site Norman Oklahoma 73069 —
Novo Nordisk Investigational Site Corvallis Oregon 97330-3737 —
Novo Nordisk Investigational Site Gaffney South Carolina 29341 —
Novo Nordisk Investigational Site Greenville South Carolina 29615 —
Novo Nordisk Investigational Site Chattanooga Tennessee 37404 —
Novo Nordisk Investigational Site Kingsport Tennessee 37660 —
Novo Nordisk Investigational Site Memphis Tennessee 38119 —
Novo Nordisk Investigational Site Dallas Texas 75230 —
Novo Nordisk Investigational Site Dallas Texas 75390-9302 —
Novo Nordisk Investigational Site Houston Texas 77074 —
Novo Nordisk Investigational Site Humble Texas 77338 —
Novo Nordisk Investigational Site Hurst Texas 76054 —
Novo Nordisk Investigational Site Katy Texas 77450 —
Novo Nordisk Investigational Site Plano Texas 75075 —
Novo Nordisk Investigational Site San Antonio Texas 78229 —
Novo Nordisk Investigational Site San Antonio Texas 78230 —
Novo Nordisk Investigational Site Shavano Park Texas 78231 —
Novo Nordisk Investigational Site Sugar Land Texas 77479 —
Novo Nordisk Investigational Site Olympia Washington 98502 —
Novo Nordisk Investigational Site Walla Walla Washington 99362-4445 —
Novo Nordisk Investigational Site Wenatchee Washington 98801-2028 —

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 68 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03989232, 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 Feb 13, 2023 · Synced Oct 7, 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 public registry record, listed eligibility criteria, and available contact information for NCT03989232 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →