Ascending Dose Study of the Safety and Tolerability of Alirocumab (SAR236553/REGN727) in Japanese Healthy Volunteers

Sanofi

Status and phase: Completed; Phase 1

Conditions: Hypercholesterolemia

Treatments: Drug: Placebo (Lyophilized formulation); Drug: Alirocumab (Lyophilized formulation); Drug: Placebo (Solution); Drug: Alirocumab (Solution)

Study type: Interventional

Funder types: Industry

Identifiers

NCT01448317

U1111-1118-1213 (Other Identifier)

TDU12190

Details and patient eligibility

About

Primary Objective:

To assess the safety and tolerability of ascending single doses of subcutaneously (SC) administered alirocumab (SAR236553/REGN727) in Japanese healthy male subjects.

Secondary Objectives:

• To assess the pharmacodynamics effect of a single SC dose of alirocumab on serum low-density lipoprotein cholesterol (LDL-C) and other lipids and apolipoproteins such as total cholesterol, high-density lipoprotein cholesterol (HDL-C), non-high-density lipoprotein cholesterol, very low-density lipoprotein cholesterol, Triglycerides, Apolipoprotein B, Apolipoprotein A1 and Lipoprotein(a).
• To assess the Pharmacokinetic profile of a single SC dose of alirocumab.
• To assess the immunogenicity of a single SC dose of alirocumab.

Full description

4 sequential dose cohorts. Single dose followed by a total observation period of 15 weeks (106 days) for each participant.

Enrollment: 32 patients

Sex: Male

Ages: 20 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy male subject, between 20 and 65 years inclusive.
• Body weight between 50.0 and 95.0 kg inclusive, body mass index between 18.0 and 30.0 kg/m² inclusive.
• Serum LDL-C levels >100 mg/dL

Exclusion criteria

• Subject indicated for the use of statins according to criteria in Adult Treatment Panel (ATP) III Guidelines as updated in 2004
• Significant concomitant illness or history of significant illness such as cardiac, renal, neurological, endocrinological, dermatological, metabolic or lymphatic disease, or any other illness or condition that would adversely affect the subject's participation in this study.
• History or presence of drug or alcohol abuse
• Smoking more than 5 cigarettes or equivalent in any 24 hour period.
• Any medication (including St John's Wort) within 14 days before the inclusion or within 5 times the elimination half-life or pharmacodynamic (PD) half-life of that drug, whichever the longest; any vaccination within the last 28 days.
• Positive reaction to any of the following tests: hepatitis B surface (HBs Ag) antigen, anti-hepatitis B core antibodies (anti-HBc Ab), anti-hepatitis C virus (anti-HCV) antibodies, human immunodeficiency virus (HIV) antigen and antibodies, syphilis.
• Elevated cholesterol due to a secondary cause such as hypothyroidism or alcohol.
• Presence or history of drug hypersensitivity
• Initiation of a new exercise routine or major change to a previous exercise routine within 4 weeks prior to Screening.
• Initiation of a new diet or major change to a previous diet within 4 weeks prior to Screening.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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32 participants in 4 patient groups

Cohort 1

Experimental group

Description:

Alirocumab dose 1 versus placebo

Treatment:

Drug: Placebo (Lyophilized formulation)

Drug: Alirocumab (Lyophilized formulation)

Cohort 2

Experimental group

Description:

Alirocumab dose 2 versus placebo

Treatment:

Drug: Placebo (Lyophilized formulation)

Drug: Alirocumab (Lyophilized formulation)

Cohort 3

Experimental group

Description:

Alirocumab dose 3 versus placebo

Treatment:

Drug: Placebo (Lyophilized formulation)

Drug: Alirocumab (Lyophilized formulation)

Cohort 4

Experimental group

Description:

Alirocumab dose 4 versus placebo

Treatment:

Drug: Placebo (Solution)

Drug: Alirocumab (Solution)