A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneous (SC) Administered Alirocumab in Healthy Chinese Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

November 29, 2016

Primary Completion Date

November 27, 2017

Study Completion Date

November 27, 2017

Conditions
Hypercholesterolemia
Interventions
DRUG

alirocumab SAR236553 (REGN727)

"Pharmaceutical form: Solution for injection~Route of administration: Subcutaneous"

DRUG

placebo

"Pharmaceutical form: Solution for injection~Route of administration: Subcutaneous"

Trial Locations (1)

100191

Investigational Site Number 156001, Beijing

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Regeneron Pharmaceuticals

INDUSTRY

lead

Sanofi

INDUSTRY