A 4-week, Randomized, Placebo-Controlled, Double-Blind, Efficacy and Safety Study of HS-25 in Adults With Primary Hypercholesterolemia

PHASE2CompletedINTERVENTIONAL
Enrollment

376

Participants

Timeline

Start Date

March 31, 2014

Primary Completion Date

September 30, 2014

Study Completion Date

December 31, 2014

Conditions
Primary Hypercholesterolemia
Interventions
DRUG

HS-25

Assigned study drug (HS-25 or placebo) is to be administered orally once daily in the morning with or without food. Treatment duration 4 weeks.

DRUG

Placebo

Assigned study drug (HS-25 or placebo) is to be administered orally once daily in the morning with or without food. Treatment duration 4 weeks.

Trial Locations (27)

85224

Chandler

Unknown

Phoenix

West Hills

Doral

Jacksonville

Miami

South Miami

Chicago

Evansville

Indianapolis

Overland Park

Louisville

Auburn

Bethesda

Methuen

Trenton

Rochester

Raleigh

Cincinnati

Tulsa

Penndel

Greensboro

Dallas

Houston

Salt Lake City

Norfolk

Richmond

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Covance

INDUSTRY

lead

Zhejiang Hisun Pharmaceutical Co. Ltd.

INDUSTRY