Safety, Tolerability and Efficacy on Low Density Lipoprotein Cholesterol (LDL-C) of Evolocumab in Participants With Human Immunodeficiency Virus (HIV) and Hyperlipidemia/Mixed Dyslipidemia

Completed · Phase 3 · Has a placebo group

Conditions studied: Subjects With Hyperlipidemia, Dyslipidemia and HIV Infection

In brief

The study is divided into 2 parts. The first part of the study will be double-blinded and will last for 24 weeks. During this time, participants will be randomized in a ratio of 2:1 to receive either evolocumab once monthly (QM) or placebo QM. The second part of the study is a 24-week open label extension period. During this time all participants will receive evolocumab QM. The clinical hypothesis is that subcutaneous evolocumab QM will be well tolerated and will result in greater reduction of low density lipoprotein cholesterol (LDL-C), defined as percent change from baseline at Week 24, compared with placebo QM in human immunodeficiency virus (HIV)-positive participants with hyperlipidemia or mixed dyslipidemia.

Key facts

Study ID

NCT02833844

Run by

Amgen

People needed

467

Starts

2017-05-22

Expected to finish

2020-01-27

Last updated by the study team

2022-07-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female ≥ 18 years of age
• Known HIV infection with stable HIV therapy for ≥ 6 months
• Cluster of differentiation 4 (CD4) ≥ 250 cells/mm\^3 for ≥ 6 months
• HIV viral load ≤ 50 copies/mL at screening and ≤ 200 copies/mL for ≥ 6 months
• Subject on stable lipid-lowering therapy for ≥ 4 weeks prior to randomization and not expected to change during the duration of study
• For subjects with known clinical atherosclerotic cardiovascular disease (ASCVD), fasting LDL-C of ≥ 70 mg/dL or non-high density lipoprotein cholesterol (non-HDL-C) ≥ 100 mg/dL. For subjects without known clinical ASCVD: fasting LDL-C of ≥ 100 mg/dL or non-HDL-C of ≥ 130 mg/dL
• Fasting triglycerides ≤ 600 mg/dL (6.8 mmol/L)

You may not qualify if…

• Taking a combination of background lipid-lowering therapy and HIV therapy known to have significant drug-drug interaction
• New York Heart Association (NYHA) III or IV heart failure, or last known left ventricular ejection fraction (LVEF) < 30%
• Known opportunistic infection/acquired immunodeficiency syndrome (AIDS) defining illness within 1 year prior to randomization
• Myocardial infarction, unstable angina, percutaneous coronary intervention, coronary artery bypass graft or stroke within 3 months
• Type 1 diabetes, new-onset or poorly controlled type 2 diabetes
• Uncontrolled hypertension
• Taken a cholesteryl ester transfer protein inhibitor in the last 12 months
• Moderate to severe renal dysfunction
• Persistent active liver disease or hepatic dysfunction (Stable chronic hepatitis C of at least 1 year duration prior to randomization is allowed)
• Malignancy (except non-melanoma skin cancers, cervical in-situ carcinoma, breast ductal carcinoma in-situ, or stage 1 prostate carcinoma) within the last 5 years prior to randomization
• Other exclusion criteria may apply.

Where it is running

• Research Site — Hartford, Connecticut, United States
• Research Site — Washington D.C., District of Columbia, United States
• Research Site — Washington D.C., District of Columbia, United States
• Research Site — Washington D.C., District of Columbia, United States
• Research Site — Miami, Florida, United States
• Research Site — Tampa, Florida, United States
• Research Site — Vero Beach, Florida, United States
• Research Site — Augusta, Georgia, United States
• Research Site — Berkley, Michigan, United States
• Research Site — Detroit, Michigan, United States
• Research Site — Southfield, Michigan, United States
• Research Site — Minneapolis, Minnesota, United States
• Research Site — St Louis, Missouri, United States
• Research Site — Camden, New Jersey, United States
• Research Site — Albany, New York, United States
• Research Site — New York, New York, United States
• Research Site — The Bronx, New York, United States
• Research Site — Cincinnati, Ohio, United States
• Research Site — Falls Church, Virginia, United States
• Research Site — Darlinghurst, New South Wales, Australia
• Research Site — East Sydney, New South Wales, Australia
• Research Site — Sydney, New South Wales, Australia
• Research Site — Fortitude Valley, Queensland, Australia
• Research Site — Melbourne, Victoria, Australia
• Research Site — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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