Study of the Long-Term Safety of Pramlintide in Subjects With Type 1 Diabetes Mellitus

Completed · Phase 3

Conditions studied: Diabetes Mellitus, Type 1

In brief

This is a multicenter, open-label extension study designed to examine the long-term safety of pramlintide treatment in subjects with type 1 diabetes who have successfully completed treatment in the parent study 137-150.

Key facts

Study ID

NCT00107107

Run by

AstraZeneca

People needed

190

Starts

2002-11-01

Expected to finish

2005-06-01

Last updated by the study team

2015-09-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The subject has completed the full dosing period in Protocol 137-150.

Where it is running

• Research Site — Tempe, Arizona, United States
• Research Site — Concord, California, United States
• Research Site — Fresno, California, United States
• Research Site — San Diego, California, United States
• Research Site — San Mateo, California, United States
• Research Site — Santa Barbara, California, United States
• Research Site — Walnut Creek, California, United States
• Research Site — Aventura, Florida, United States
• Research Site — Fort Myers, Florida, United States
• Research Site — New Port Richey, Florida, United States
• Research Site — Tallahassee, Florida, United States
• Research Site — Atlanta, Georgia, United States
• Research Site — Indianapolis, Indiana, United States
• Research Site — Detroit, Michigan, United States
• Research Site — Grand Rapids, Michigan, United States
• Research Site — City of Saint Peters, Missouri, United States
• Research Site — Butte, Montana, United States
• Research Site — Durham, North Carolina, United States
• Research Site — Columbus, Ohio, United States
• Research Site — Portland, Oregon, United States
• Research Site — Camp Hill, Pennsylvania, United States
• Research Site — Nashville, Tennessee, United States
• Research Site — Irving, Texas, United States
• Research Site — San Antonio, Texas, United States
• Research Site — Renton, Washington, United States

Full record on ClinicalTrials.gov

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