Overview

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

Status:
Completed
Trial end date:
2008-04-01
Target enrollment:
Participant gender:
Summary
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.
Phase:
Phase 4
Details
Lead Sponsor:
AstraZeneca
Treatments:
Insulin
Insulin Aspart
Insulin Detemir
Insulin Glargine
Insulin glulisine
Insulin Lispro
Insulin, Globin Zinc
Insulin, Short-Acting
Pramlintide