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Completed Phase 3 Interventional Results available

Safety and Efficacy of Exenatide as Monotherapy and Adjunctive Therapy to Oral Antidiabetic Agents in Adolescents With Type 2 Diabetes

ClinicalTrials.gov ID: NCT00658021

Public ClinicalTrials.gov record NCT00658021. 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 Jun 26, 2026, 1:48 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

Safety and Efficacy of Exenatide as Monotherapy and Adjunctive Therapy to Oral Antidiabetic Agents in Adolescents With Type 2 Diabetes.

Study identification

NCT ID
NCT00658021
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
122 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Exenatide Drug

Drug

Eligibility (public fields only)

Age range
10 Years to 17 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
May 29, 2008
Primary completion
Apr 17, 2019
Completion
Mar 31, 2020
Last update posted
Nov 30, 2020

2008 – 2020

United States locations

U.S. sites
31
U.S. states
18
U.S. cities
30
Facility City State ZIP Site status
Research Site Birmingham Alabama 35233
Research Site Tucson Arizona 85724
Research Site Los Angeles California 90048
Research Site Montclair California 91763
Research Site Sacramento California 95819
Research Site San Diego California 92123
Research Site Santa Ana California 92707
Research Site Aurora Colorado 80045
Research Site Melbourne Florida 32901
Research Site Miami Florida 33144
Research Site Miami Lakes Florida 33014
Research Site Orlando Florida 32806
Research Site Pensacola Florida 32504
Research Site Tallahassee Florida 32308
Research Site Dalton Georgia 30721
Research Site Chicago Illinois 60612
Research Site Chicago Illinois 60637
Research Site Indianapolis Indiana 46202
Research Site Wichita Kansas 67226
Research Site Dearborn Michigan 48124
Research Site Kansas City Missouri 64108
Research Site St Louis Missouri 63104
Research Site Reno Nevada 89502
Research Site Jamaica New York 11432
Research Site Greenville North Carolina 27834
Research Site Raleigh North Carolina 27610
Research Site Oklahoma City Oklahoma 73104-5008
Research Site Memphis Tennessee 38401
Research Site Dallas Texas 75235
Research Site San Antonio Texas 78207
Research Site Spokane Washington 99202

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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00658021, 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 Nov 30, 2020 · Synced Jun 26, 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 NCT00658021 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →