Efficacy and Safety Study of JTT-705 in Combination With Pravastatin 40 mg in Patients With Type II Hyperlipidemia

PHASE2CompletedINTERVENTIONAL
Enrollment

155

Participants

Timeline

Start Date

June 30, 2002

Primary Completion Date

April 30, 2003

Study Completion Date

March 31, 2004

Conditions
Type II Hyperlipidemia
Interventions
DRUG

JTT-705 600 mg and pravastatin 40 mg

"* JTT-705 300 mg tablets, 600 mg dose, 2 tablets, oral, once daily, immediately following breakfast and/or assessment~* Pravastatin 40 mg tablets, 40 mg dose, one tablet, oral, once daily, at bedtime"

DRUG

JTT-705 300 mg and pravastatin 40 mg

"* JTT-705 300 mg tablets, 300 mg dose, 1 tablet, oral, once daily, immediately following breakfast and/or assessment~* Placebo tablets, one tablet, oral, once daily, immediately following breakfast and/or assessments~* Pravastatin 40 mg tablets, 40 mg dose, one tablet, oral, once daily, at bedtime"

DRUG

Placebo and pravastatin 40 mg

"* Placebo tablets, 2 tablets, oral, once daily, immediately following breakfast and/or assessments~* Pravastatin 40 mg tablets, 40 mg dose, one tablet, oral, once daily, at bedtime"

Trial Locations (1)

Unknown

Amsterdam

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Akros Pharma Inc.

INDUSTRY

NCT00688896 - Efficacy and Safety Study of JTT-705 in Combination With Pravastatin 40 mg in Patients With Type II Hyperlipidemia | Biotech Hunter | Biotech Hunter