To Evaluate Safety and Tolerability After Multiple Oral Doses of AZD1656 in Type 2 Diabetes Patients on Top of Insulin

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

September 30, 2008

Primary Completion Date

March 31, 2009

Study Completion Date

March 31, 2009

Conditions
Type 2 Diabetes
Interventions
DRUG

AZD1656

Dose titration of oral suspension to a tolerable dose in 2-3 dose steps. Investigational product given twice daily for eight days.

DRUG

Placebo

Dosing to match AZD1656

Trial Locations (1)

Unknown

Research Site, Chula Vista

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY