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Study Complete
Sponsor ID
20130286

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

Sponsor ID
20130286
Clinicaltrials.gov ID
NCT02833844
EUCTIS ID
N/A
EudraCT ID
2015-004735-12
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Study Details

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.

Additional Study Details

Phase
Phase 3
Product
Evolocumab
Type
Interventional
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Enrollment
467
Additional Study Details

Protocol Summary

Primary Outcome Measures

Percent Change From Baseline in LDL-C at Week 24

Timeframe: Baseline, Week 24

Secondary Outcome Measures

Change From Baseline in LDL-C

Timeframe: Baseline, Week 24

Percentage of Participants Acheiving LDL-C < 70 mg/dL (1.8 mmol/L) at Week 24

Timeframe: Week 24

Percentage of Participants With an LDL-C Response (50% Reduction of LDL-C From Baseline) at Week 24

Timeframe: Baseline, Week 24

Percent Change From Baseline in Non-High-Density Lipoprotein Cholesterol (HDL-C) at Week 24

Timeframe: Baseline, Week 24

Percent Change From Baseline in Apolipoprotein B (ApoB) at Week 24

Timeframe: Baseline, Week 24

Percent Change From Baseline in Total Cholesterol (TC) at Week 24

Timeframe: Baseline, Week 24

Percent Change From Baseline in Lipoprotein(a) (Lp[a])

Timeframe: Baseline, Week 24

Percent Change From Baseline in Triglycerides at Week 24

Timeframe: Baseline, Week 24

Percent Change From Baseline in HDL-C at Week 24

Timeframe: Bseline, Week 24

Percent Change From Baseline in Very Low-Density Lipoprotein Cholesterol (VLDL-C) at Week 24

Timeframe: Baseline, Week 24

Locations

Location
Status
Contact Us
Location
Research Site
Sydney, NSW, Australia, 2010
Status
Recruiting
Location
Research Site
New York, NY, United States, 10029
Status
Recruiting
Location
Research Site
East Sydney, NSW, Australia, 2010
Status
Recruiting
Location
Research Site
Berkley, MI, United States, 48072
Status
Recruiting
Location
Research Site
Fortitude Valley, QLD, Australia, 4006
Status
Recruiting
Location
Research Site
Vero Beach, FL, United States, 32960
Status
Recruiting
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Study Info
Age
18+ years
Condition
  • Heart, Blood & Circulatory - Other
    • Sex
    All
    Trial Dates
    May 2017 - Jul 2019
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    - 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)
    Exclusion Criteria:
    - 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.