A Safety Study of BMS-852927 in Subjects With Hypercholesterolemia

PHASE1TerminatedINTERVENTIONAL
Enrollment

97

Participants

Timeline

Start Date

November 30, 2012

Primary Completion Date

June 30, 2013

Study Completion Date

June 30, 2013

Conditions
Hypercholesterolemia
Interventions
DRUG

BMS-852927

Capsules, Oral, 0.25 mg, Once daily, 28 days

DRUG

BMS-852927

Capsules, Oral, 1.0 mg, Once daily, 28 days

DRUG

BMS-852927

Capsules, Oral, 2.5 mg, Once daily, 28 days

DRUG

Placebo

Capsules, Oral, 0 mg, Once daily, 28 days

Trial Locations (8)

10117

Local Institution, Berlin

41460

Local Institution, Neuss

L6T 0G1

Local Institution, Brampton

M4G 3E8

Local Institution, Toronto

H9R 4S3

Local Institution, Pointe-Claire

G1N 4V3

Local Institution, Québec

G3K 2P8

Local Institution, Québec

G6P 6P6

Local Institution, Victoriaville

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY