AZD9056 Relative Bioavailability Study

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

May 31, 2009

Study Completion Date

July 31, 2009

Conditions
Healthy
Interventions
DRUG

AZD9056 formulation Phase III 50 mg (T)

Given as 50 mg tablet (T)

DRUG

AZD9056 formulation Phase IIb 50 mg (R)

Given as 50 mg tablet (R)

DRUG

AZD9056 formulation Phase III 200 mg (T)

Given as 400 mg (2 x 200 mg tablet (T))

DRUG

AZD9056 formulation Phase IIb 200mg (R)

Given as 400 mg (2 x 200 mg tablet (R))

Trial Locations (1)

Unknown

Research Site, Manchester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY