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Completed Phase 3 Interventional Results available

Phase III Study to Evaluate Safety and Efficacy of Added Exenatide Versus Placebo to Titrated Basal Insulin Glargine in Inadequately Controlled Patients With Type II Diabetes Mellitus

ClinicalTrials.gov ID: NCT02229383

Public ClinicalTrials.gov record NCT02229383. 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 11, 2026, 2:24 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 Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase 3 Trial to Evaluate the Safety and Efficacy of Once Weekly Exenatide Therapy Added to Titrated Basal Insulin Glargine Compared to Placebo Added to Titrated Basal Insulin Glargine in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Basal Insulin Glargine With or Without Metformin

Brief summary

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

Study D5553C00002 is a multicenter, randomized, double-blind, placebo-controlled, parallel group, Phase 3 study to compare the safety and efficacy of exenatide once weekly (EQW) added to titrated basal insulin glargine with or without metformin to placebo added to titrated basal insulin glargine with or without metformin in patients with type 2 diabetes mellitus (T2DM). Eligible patients will be randomized at Visit 5 (Day 1) to receive either EQW added to titrated basal insulin glargine, with or without metformin ≥1500 mg/day, or placebo added to titrated basal insulin glargine, with or without metformin ≥1500 mg/day, during the 28-week treatment period.

Study identification

NCT ID
NCT02229383
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
464 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 130 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
Sep 5, 2014
Primary completion
Aug 28, 2016
Completion
Aug 28, 2016
Last update posted
Jan 7, 2019

2014 – 2016

United States locations

U.S. sites
68
U.S. states
23
U.S. cities
59
Facility City State ZIP Site status
Research Site Birmingham Alabama 35235
Research Site Huntsville Alabama 35801
Research Site Muscle Shoals Alabama 35662
Research Site Tempe Arizona 85283
Research Site Chino California 91710
Research Site Chula Vista California 91910
Research Site El Cajon California 92020
Research Site Fresno California 93720
Research Site Long Beach California 90807
Research Site Los Angeles California 90057
Research Site Mission Hills California 91345
Research Site Tustin California 92780
Research Site West Hills California 91307
Research Site Boynton Beach Florida 33437
Research Site Brooksville Florida 34601
Research Site Chiefland Florida 32626
Research Site Clearwater Florida 33765
Research Site Coral Gables Florida 33134
Research Site Fort Lauderdale Florida 33316
Research Site Hialeah Florida 33012
Research Site Jacksonville Florida 32256
Research Site Jacksonville Florida 32277
Research Site Miami Florida 33125
Research Site Miami Florida 33126
Research Site Miami Florida 33133
Research Site Miami Florida 33142
Research Site Miami Florida 33175
Research Site North Miami Beach Florida 33162
Research Site Orlando Florida 32806
Research Site Tampa Florida 33603
Research Site Columbus Georgia 31406
Research Site Chicago Illinois 60607
Research Site Avon Indiana 46123
Research Site Evansville Indiana 47714
Research Site Franklin Indiana 46131
Research Site Newton Kansas 67114
Research Site Monroe Louisiana 71203
Research Site New Orleans Louisiana 70112
Research Site Hazelwood Missouri 63042
Research Site Bellevue Nebraska 68005
Research Site Omaha Nebraska 68114
Research Site Haddon Heights New Jersey 08035
Research Site Mooresville North Carolina 28117
Research Site Morehead City North Carolina 28557
Research Site Morganton North Carolina 28655
Research Site Cincinnati Ohio 45242
Research Site Cleveland Ohio 44122
Research Site Dayton Ohio 45417
Research Site Medford Oregon 97504
Research Site Philadelphia Pennsylvania 91307
Research Site Greer South Carolina 29651
Research Site Spartanburg South Carolina 29303
Research Site Dakota Dunes South Dakota 57049
Research Site Johnson City Tennessee 37604
Research Site Kingsport Tennessee 37660
Research Site Austin Texas 78705
Research Site Dallas Texas 75208
Research Site Dallas Texas 75230
Research Site Houston Texas 77030
Research Site Houston Texas 77070
Research Site Houston Texas 77079
Research Site Houston Texas 77090
Research Site Clinton Utah 84015
Research Site Ogden Utah 84405
Research Site Salt Lake City Utah 84102
Research Site Manassas Virginia 20110
Research Site Richmond Virginia 23294
Research Site Port Orchard Washington 98366

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 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02229383, 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 7, 2019 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02229383 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →