A Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD8233 in Healthy Male Subjects With Increased Elevated LDL-C Levels.

PHASE1CompletedINTERVENTIONAL
Enrollment

73

Participants

Timeline

Start Date

August 3, 2018

Primary Completion Date

December 19, 2020

Study Completion Date

December 19, 2020

Conditions
Hypercholesterolemia
Interventions
DRUG

AZD8233

Randomized subjects will receive single SC dose of AZD8233 (dose 1, dose 2, dose 3, dose 4 and dose 5) injection.

Trial Locations (1)

91206

Research Site, Glendale

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY