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Completed Phase 4 Interventional Results available

Study to Evaluate the Effect of BYDUREON on 24-hour Glucose Control in Metformin Treated Patients With Type 2 Diabetes.

ClinicalTrials.gov ID: NCT02288273

Public ClinicalTrials.gov record NCT02288273. 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 Jul 23, 2026, 12:41 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 Randomized Double-blind, Parallel-group Study to Evaluate the Effect of BYDUREON Compared With Placebo on 24-hour Glucose Control in Metformin-treated Patients With Type 2 Diabetes

Study identification

NCT ID
NCT02288273
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AstraZeneca
Industry
Enrollment
239 participants

Conditions and interventions

Interventions

  • Bydureon Drug
  • Placebo Drug

Drug

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 30, 2014
Primary completion
Jul 31, 2015
Completion
Jul 31, 2015
Last update posted
Jan 26, 2017

2014 – 2015

United States locations

U.S. sites
29
U.S. states
16
U.S. cities
29
Facility City State ZIP Site status
Research Site Anaheim California
Research Site Chino California
Research Site Los Angeles California
Research Site North Hollywood California
Research Site Santa Ana California
Research Site Spring Valley California
Research Site Tustin California
Research Site Walnut Creek California
Research Site Hollywood Florida
Research Site Miami Florida
Research Site Port Orange Florida
Research Site Marietta Georgia
Research Site Chicago Illinois
Research Site Edina Minnesota
Research Site St Louis Missouri
Research Site Butte Montana
Research Site Las Vegas Nevada
Research Site Franklin Ohio
Research Site Marion Ohio
Research Site Oklahoma City Oklahoma
Research Site Mt. Pleasant South Carolina
Research Site Rapid City South Dakota
Research Site Corpus Christi Texas
Research Site Houston Texas
Research Site Katy Texas
Research Site Salt Lake City Utah
Research Site Burke Virginia
Research Site Manassas Virginia
Research Site Olympia Washington

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 NCT02288273, 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 Jan 26, 2017 · Synced Jul 23, 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 protocol, eligibility criteria, and contact information for NCT02288273 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →