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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 Oct 22, 2026, 3:45 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

Brief summary

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

This will be a randomized, open label, parallel group, multicenter study. There will be two phases in the study. Phase 1 (Baseline to Week 24) will compare the efficacy and safety of regimens of basal insulin intensified with either Symlin or rapid acting insulin in patients with type 2 diabetes who have either been on a prior regimen of insulin for less than 6 months and were taking less than 50 U total of insulin per day OR are candidates for the initiation of insulin therapy. The purpose of Phase 2 (Week 24 to Week 36) is to explore further intensification of diabetes regimens in patients failing to achieve HbA1c \<=6.5% at Week 24.

Study identification

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

Conditions and interventions

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
May 2007 (Type not available)
Primary completion
Apr 2008 (Actual)
Completion
Apr 2008 (Actual)
Last update posted
Apr 14, 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 14, 2015 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00467649 live on ClinicalTrials.gov.

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