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

PHASE4CompletedINTERVENTIONAL
Enrollment

112

Participants

Timeline

Start Date

May 31, 2007

Primary Completion Date

April 30, 2008

Study Completion Date

April 30, 2008

Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG

pramlintide acetate (Symlin)

subcutaneous injection (60 mcg or 120 mcg), immediately prior to major meals

DRUG

rapid acting insulin (Humalog® [insulin lispro], Novolog® [insulin aspart], or Apidra® [insulin glulisine])

subcutaneous injection, dosing based on titration guidelines

DRUG

basal insulin (Lantus® [insulin glargine], or Levemir® [insulin detemir])

subcutaneous injection, dosing based on titration guidelines

Trial Locations (37)

Unknown

Research Site, Northport

Research Site, Phoenix

Research Site, Loma Linda

Research Site, Aurora

Research Site, Hollywood

Research Site, Maitland

Research Site, Miami

Research Site, North Miami Beach

Research Site, Plantation

Research Site, Roswell

Research Site, Peoria

Research Site, Indianapolis

Research Site, Wichita

Research Site, Lexington

Research Site, Baton Rouge

Research Site, Baltimore

Research Site, Detroit

Research Site, Grand Rapids

Research Site, Jackson

Research Site, St Louis

Research Site, Butte

Research Site, Las Vegas

Research Site, Hamilton

Research Site, Albuquerque

Research Site, Albany

Research Site, Staten Island

Research Site, Mentor

Research Site, Portland

Research Site, Bridgeville

Research Site, Philadelphia

Research Site, Aiken

Research Site, Bartlett

Research Site, Nashville

Research Site, Austin

Research Site, Dallas

Research Site, Olympia

Research Site, Spokane

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY