To Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD8233 After Multiple Dose Administration in Subjects With Dyslipidemia

PHASE1CompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

November 21, 2019

Primary Completion Date

June 7, 2021

Study Completion Date

June 7, 2021

Conditions
Dyslipidemia
Interventions
DRUG

AZD8233 subcutaneous injection

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

DRUG

Placebo

Randomized subjects will receive SC dose of placebo injection.

Trial Locations (7)

21225

Research Site, Brooklyn

32127

Research Site, Port Orange

32216

Research Site, Jacksonville

32806

Research Site, Orlando

91206

Research Site, Glendale

91911

Research Site, Chula Vista

91942

Research Site, La Mesa

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY