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Completed Phase 2 Interventional Results available

A Research Study Looking at How Well a Combination of the Medicines Semaglutide and NNC0480-0389 Works in People With Type 2 Diabetes

ClinicalTrials.gov ID: NCT05144984

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT05144984. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 14, 2026, 1:27 PM EST

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Official title

Investigation of the Safety and Efficacy of Semaglutide s.c. in Combination With NNC0480-0389 in Participants With Type 2 Diabetes - a Dose Finding Study

Brief summary

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

This study is looking at semaglutide in combination with a potential new medicine (NNC0480-0389) in people with type 2 diabetes. The study is being conducted to see how well semaglutide, in combination with different doses of NNC0480-0389, work to lower blood sugar levels. Results from this study will be used to select the doses of the two medicines for other studies. Participants will either get: Semaglutide (a medicine doctors can already prescribe for treatment of type 2 diabetes) in combination with NNC0480-0389 (a potential new medicine) or placebo (a 'dummy' medicine that looks like the medicines but without any medicine). NNC0480-0389 alone, or semaglutide alone which treatment participant get is decided by chance. Participant will need to take 2-3 injections once every week during the study. One injection will be with semaglutide or placebo and 1-2 injections will be with NNC0480-0389 or placebo. Participant must inject the study medicines themself into the stomach, thigh, or upper arm. The study will last for about 41weeks. Participant will have 20 clinic visits. Participant will have blood samples taken at all clinic visits. At 3 clinic visits, participant will also have an electrocardiogram (ECG). This is a test to check participants heart. Participant will have their eyes checked before or at the start of the study and at the end of the study. Women can only take part in the study if they are not able to become pregnant

Study identification

NCT ID
NCT05144984
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
500 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Nov 29, 2021 (Actual)
Primary completion
Feb 13, 2023 (Actual)
Completion
Mar 23, 2023 (Actual)
Last update posted
Apr 9, 2026

2021 – 2023

United States locations

U.S. sites
71
U.S. states
29
U.S. cities
66
Facility City State ZIP Site status
Pinnacle Research Group LLC Anniston Alabama 36207 —
Synexus Clinical Research Glendale Arizona 85308 —
University of Arizona/Banner Health Phoenix Arizona 85006 —
American Clinical Trials Buena Park California 90620 —
San Fernando Valley Hlth Inst, LLC Canoga Park California 91304 —
Velocity Clin Res-Chula Vista Chula Vista California 91911 —
Headlands Research California, LLC Escondido California 92025 —
Valley Research Fresno California 93720 —
Providence Medical Foundation Fullerton California 92835 —
Velocity Clinical Research San Diego La Mesa California 91942 —
First Valley Med Grp Lancaster Lancaster California 93534 —
Torrance Clin Res Inst, Inc. Lomita California 90717 —
Velocity Clin Res Los Angeles Los Angeles California 90017 —
Valley Clinical Trials, Inc. Northridge California 91325 —
Artemis Insitute for Clin Res Riverside California 92503 —
Artemis Institute for Clin Res San Diego California 92103 —
Shahram Jacobs MD Inc. Sherman Oaks California 91403 —
Diablo Clinical Research, Inc. Walnut Creek California 94598 —
Northeast Research Institute Jacksonville Florida 32204 —
Reyes Clinical Research, Inc Miami Florida 33175 —
South Broward Research LLC Miramar Florida 33027 —
Clinical Trial Res Assoc,Inc Plantation Florida 33324 —
Progressive Medical Research Port Orange Florida 32127 —
Headlands Research - Sarasota Sarasota Florida 34243 —
Appalachian Clinical Res LLC Adairsville Georgia 30103 —
Solaris Clinical Research Meridian Idaho 83646 —
Cedar-Crosse Research Center Chicago Illinois 60607 —
Macoupin Research Group Gillespie Illinois 62033 —
UnityPoint Health-Diabetes Care Center Peoria Illinois 61603 —
Clin Invest Spec, Inc Wauconda Illinois 60084 —
Iowa Diabetes & Endo Res Ctr West Des Moines Iowa 50265 —
Cotton O'Neil Diab & Endo Ctr Topeka Kansas 66606 —
The Research Group of Lexington LLC Lexington Kentucky 40503 —
L-MARC Research Center Louisville Kentucky 40213 —
Centex Studies, Inc._Lake Charles Lake Charles Louisiana 70601 —
Endo And Metab Cons Rockville Maryland 20852 —
Brigham & Women's Hospital Boston Massachusetts 02115-5804 —
Arcturus HC PLC Troy Med Res Troy Michigan 48098 —
StudyMetrix Research LLC City of Saint Peters Missouri 63303 —
Mercury Str Med Grp, PLLC Butte Montana 59701 —
Princeton Endo Assoc Princeton New Jersey 08540 —
Premier Research Inc. Trenton New Jersey 08611 —
AMC Community Endocrinology Albany New York 12203 —
Mid Hudson Med Res-New Windsor New Windsor New York 12553 —
University of North Carolina Chapel Hill North Carolina 27514 —
PharmQuest Life Sciences LLC Greensboro North Carolina 27408 —
Physicians East Endocrinology Greenville North Carolina 27834 —
Piedmont Healthcare/Research Statesville North Carolina 28625 —
Lillestol Research LLC Fargo North Dakota 58104 —
Albert J Weisbrot Mason Ohio 45040-6815 —
Advanced Med Res Maumee Maumee Ohio 43537 —
Intend Research Norman Oklahoma 73069 —
Essential Medical Research LLC Tulsa Oklahoma 74137 —
CCT Research Hatboro Pennsylvania 19040 —
Preferred Primary Care Physicians_Pittsburgh Pittsburgh Pennsylvania 15236 —
Spartanburg Medical Research Spartanburg South Carolina 29303 —
Chattanooga Medical Research, LLC Chattanooga Tennessee 37404 —
Clinical Neuroscience Solutions Memphis Tennessee 38119 —
Velocity Clinical Res-Dallas Dallas Texas 75230 —
UT Southwestern Med Cntr Dallas Texas 75390-9302 —
Centex Studies, Inc. Houston Texas 77058 —
Juno Research, LLC Houston Texas 77074 —
Southwest Clinical Trials Houston Texas 77074 —
Centex Studies Houston Texas 77090 —
Quality Research Inc San Antonio Texas 78209 —
VIP Trials_San Antonio San Antonio Texas 78230 —
Consano Clinical Research, LLC Shavano Park Texas 78231 —
Simcare Medical Research, LLC Sugar Land Texas 77478 —
Advanced Research Institute Ogden Utah 84405 —
York Clinical Research LLC Norfolk Virginia 23504 —
Capital Clin Res Ctr,LLC 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 58 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05144984, 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 9, 2026 · Synced Nov 14, 2026

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