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Completed Phase 4 Interventional Results available

A Study to Characterize Regimens of Basal Insulin Intensified With Either Symlin® or Rapid Acting Insulin in Patients With Type 2 Diabetes

ClinicalTrials.gov ID: NCT00467649

Public ClinicalTrials.gov record NCT00467649. 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 11, 2026, 9:13 PM 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 Phase 4, Randomized, Open Label, Parallel Group, Multicenter Study to Characterize Regimens of Basal Insulin Intensified With Either Symlin® or Rapid Acting Insulin in Patients With Type 2 Diabetes

Study identification

NCT ID
NCT00467649
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AstraZeneca
Industry
Enrollment
112 participants

Conditions and interventions

Interventions

  • basal insulin (Lantus® [insulin glargine], or Levemir® [insulin detemir]) Drug
  • pramlintide acetate (Symlin) Drug
  • rapid acting insulin (Humalog® [insulin lispro], Novolog® [insulin aspart], or Apidra® [insulin glulisine]) 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
Apr 30, 2007
Primary completion
Mar 31, 2008
Completion
Mar 31, 2008
Last update posted
Apr 13, 2015

2007 – 2008

United States locations

U.S. sites
37
U.S. states
27
U.S. cities
37
Facility City State ZIP Site status
Research Site Northport Alabama
Research Site Phoenix Arizona
Research Site Loma Linda California
Research Site Aurora Colorado
Research Site Hollywood Florida
Research Site Maitland Florida
Research Site Miami Florida
Research Site North Miami Beach Florida
Research Site Plantation Florida
Research Site Roswell Georgia
Research Site Peoria Illinois
Research Site Indianapolis Indiana
Research Site Wichita Kansas
Research Site Lexington Kentucky
Research Site Baton Rouge Louisiana
Research Site Baltimore Maryland
Research Site Detroit Michigan
Research Site Grand Rapids Michigan
Research Site Jackson Mississippi
Research Site St Louis Missouri
Research Site Butte Montana
Research Site Las Vegas Nevada
Research Site Hamilton New Jersey
Research Site Albuquerque New Mexico
Research Site Albany New York
Research Site Staten Island New York
Research Site Mentor Ohio
Research Site Portland Oregon
Research Site Bridgeville Pennsylvania
Research Site Philadelphia Pennsylvania
Research Site Aiken South Carolina
Research Site Bartlett Tennessee
Research Site Nashville Tennessee
Research Site Austin Texas
Research Site Dallas Texas
Research Site Olympia Washington
Research Site Spokane 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 NCT00467649, 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 Apr 13, 2015 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00467649 live on ClinicalTrials.gov.

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