A Phase I Study to Evaluate Safety, Tolerability and Pharmacokinetics of ONO-4053 in Healthy Volunteers

PHASE1TerminatedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

June 30, 2011

Primary Completion Date

July 31, 2011

Conditions
Healthy Adult Subjects
Interventions
DRUG

ONO-4053

Part A: ONO-4053 doses proposed are 1 mg, 3 mg, 10 mg, 30 mg, 100 mg, 300 mg, 600 mg as a single dose administered by mouth once daily

DRUG

Placebo

Placebo to match ONO-4053 tablets dosed in a similar manner to ONO-4053

Trial Locations (1)

LS2 9LH

Leeds Clinical Site, Leeds

Sponsors
All Listed Sponsors
lead

Ono Pharmaceutical Co. Ltd

INDUSTRY