AZD8075 Study to Assess the Safety, Tolerability and Pharmacokinetics of Multiple Ascending Oral Doses of AZD8075 in Healthy Male Volunteers

PHASE1WithdrawnINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

January 31, 2009

Primary Completion Date

January 31, 2009

Study Completion Date

January 31, 2009

Conditions
Healthy
Interventions
DRUG

AZD8075

single dose, oral suspension, on Day 1. Repeated dosing will commence on Day 3 once daily for 14 days. The planned starting dose will be 35 mg with up to 2 dose escalations not exceeding AstraZeneca pre-defined upper exposure limits or the exposure obtained so far in the SAD study.

DRUG

Placebo

Oral suspension

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY