Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
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 Oct 30, 2026, 4:44 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 6, 2014 (Actual)
Primary completion
Aug 29, 2016 (Actual)
Completion
Aug 29, 2016 (Actual)
Last update posted
Jan 8, 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 8, 2019 · Synced Oct 30, 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 NCT02229383 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →