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Completed Phase 2 Interventional

A Study of Once-Daily NNC0090-2746 in Participants With Type 2 Diabetes Inadequately Controlled With Metformin

ClinicalTrials.gov ID: NCT02205528

Public ClinicalTrials.gov record NCT02205528. 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 May 12, 2026, 4:40 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

A Multi-Center, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Phase 2a Study With an Open-Label Active Group to Assess the Efficacy and Safety of Once-Daily NNC0090-2746 in Type 2 Diabetic Patients Inadequately Controlled With Metformin

Study identification

NCT ID
NCT02205528
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
108 participants

Conditions and interventions

Interventions

  • Liraglutide Drug
  • Metformin Drug
  • NNC0090-2746 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
Not listed
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
Aug 17, 2014
Primary completion
Sep 14, 2015
Completion
Sep 14, 2015
Last update posted
Jul 20, 2020

2014 – 2015

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Novo Nordisk Investigational Site Chino California 91710
Novo Nordisk Investigational Site Hawaiian Gardens California 90716
Novo Nordisk Investigational Site Los Angeles California 90057
Novo Nordisk Investigational Site Spring Valley California 91978
Novo Nordisk Investigational Site Hialeah Florida 33012
Novo Nordisk Investigational Site Port Orange Florida 32127
Novo Nordisk Investigational Site Sanford Florida 32771
Novo Nordisk Investigational Site Chicago Illinois 60607
Novo Nordisk Investigational Site Evanston Illinois 60201
Novo Nordisk Investigational Site Oxon Hill Maryland 20745
Novo Nordisk Investigational Site Berlin New Jersey 08009
Novo Nordisk Investigational Site Albuquerque New Mexico 87102
Novo Nordisk Investigational Site Greensboro North Carolina 27408
Novo Nordisk Investigational Site Cincinnati Ohio 45227
Novo Nordisk Investigational Site Tulsa Oklahoma 74136
Novo Nordisk Investigational Site Eugene Oregon 97404
Novo Nordisk Investigational Site Knoxville Tennessee 37920
Novo Nordisk Investigational Site Corpus Christi Texas 78404
Novo Nordisk Investigational Site Houston Texas 77074
Novo Nordisk Investigational Site Manassas Virginia 20110

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02205528, 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 20, 2020 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02205528 live on ClinicalTrials.gov.

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