Clinical Utility and Safety of Pramlintide in Subjects With Type 1 and Type 2 Diabetes Mellitus

PHASE3CompletedINTERVENTIONAL
Enrollment

400

Participants

Timeline

Start Date

April 30, 2003

Primary Completion Date

June 30, 2005

Study Completion Date

June 30, 2005

Conditions
Type 1 Diabetes MellitusType 2 Diabetes Mellitus
Interventions
DRUG

pramlintide acetate

Pramlintide (0.6 mg/mL) in 5.0-mL multiple-draw glass vials for SC injection for 12weekes and after Pramlintide (1.0 mg/mL) 1.5 mL pen-cartridge. Subjects who do not switch to the pen-cartridge device at Week 12 will continue to administer pramlintide using a syringe and vial.

Trial Locations (48)

Unknown

Research Site, Anaheim

Research Site, Escondido

Research Site, La Jolla

Research Site, Los Gatos

Research Site, San Francisco

Research Site, Torrance

Research Site, New Britain

Research Site, Norwalk

Research Site, Norwich

Research Site, Washington D.C.

Research Site, Clearwater

Research Site, Orlando

Research Site, Columbus

Research Site, Honolulu

Research Site, Idaho Falls

Research Site, Indianapolis

Research Site, Vincennes

Research Site, Topeka

Research Site, Wichita

Research Site, Lexington

Research Site, Baltimore

Research Site, Bloomfield Hills

Research Site, Tupelo

Research Site, Las Vegas

Research Site, Reno

Research Site, Moorestown

Research Site, Neptune City

Research Site, Roseland

Research Site, New York

Research Site, Williston Park

Research Site, Yonkers

Research Site, Greenville

Research Site, Lakewood

Research Site, Westlake

Research Site, Portland

Research Site, Philadelphia

Research Site, Wilkes-Barre

Research Site, Charleston

Research Site, Sumter

Research Site, Chattanooga

Research Site, Knoxville

Research Site, Memphis

Research Site, Nashville

Research Site, Arlington

Research Site, Dallas

Research Site, Olympia

Research Site, Madison

Research Site, Milwaukee

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY