Clinical Trials · NCT00042458

Evaluation of Dose-titration of Pramlintide During Initiation of Therapy in Patients Trying to Improve Glucose Control

CompletedPhase 3Pramlintide (Approved)
Phase
Phase 3
Recruitment status
Completed
Sponsor
AstraZeneca
Enrollment
296
Start date
Apr 2002
Locations
33 sites, United States
Primary endpoint
- To investigate the safety of pramlintide treatment employing dose titration upon initiation of pramlintide followed by insulin dose optimization in subjects with type 1 diabetes.
View Pramlintide compound reference