Evaluation of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TA-8995 With Single, Escalating Doses in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

96

Participants

Timeline

Start Date

March 31, 2008

Primary Completion Date

June 30, 2009

Study Completion Date

June 30, 2009

Conditions
Dyslipidemia
Interventions
DRUG

TA-8995

TA-8905 5, 10, 25, 50 (fasted and fed), 100 and 150 mg

DRUG

TA-8995

Drug: TA-8995 25 mg

DRUG

TA-8995

Drug: TA-8995 25 mg

DRUG

TA-8995

Drug: TA-8995 25, 50, 100 and 150 mg

DRUG

Placebo

Single ascending dose in Caucasian men

DRUG

Placebo

Age-effect in Caucasian men

DRUG

Placebo

Gender-effect in Caucasian women

DRUG

Placebo

Single ascending dose in Japanese men

Trial Locations (1)

NW10 7EW

Hammersmith Medicines Research (HMR), London

All Listed Sponsors
lead

Mitsubishi Tanabe Pharma Corporation

INDUSTRY