Effect of IL--1β Inhibition on Inflammation and Cardiovascular Risk
Status: | Active, not recruiting |
---|---|
Conditions: | Peripheral Vascular Disease, HIV / AIDS |
Therapuetic Areas: | Cardiology / Vascular Diseases, Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 40 - Any |
Updated: | 6/6/2018 |
Start Date: | September 2015 |
End Date: | June 2020 |
The purpose of this study is to evaluate the effects of IL-1β inhibition on safety, measures
of systemic and vascular inflammation and endothelial function (all indicators of
cardiovascular risk) in treated and suppressed HIV infected individuals This study will
assess the safety and effects of canakinumab on endothelial function (assessed by
flow-mediated vasodilation [FMD] of the brachial artery), vascular inflammation (assessed by
FDG-PET/CT scanning), key inflammatory markers of cardiovascular disease (CVD) risk
(high-sensitivity C-reactive protein [hsCRP]), interleukin-6 (IL-6), soluble CD163 (sCD163),
D-dimer, T-cell and monocyte activation in the blood, and size of the HIV reservoir. 20
individuals will receive a single dose of 150mg canakinumab with follow-up for 18 weeks.
of systemic and vascular inflammation and endothelial function (all indicators of
cardiovascular risk) in treated and suppressed HIV infected individuals This study will
assess the safety and effects of canakinumab on endothelial function (assessed by
flow-mediated vasodilation [FMD] of the brachial artery), vascular inflammation (assessed by
FDG-PET/CT scanning), key inflammatory markers of cardiovascular disease (CVD) risk
(high-sensitivity C-reactive protein [hsCRP]), interleukin-6 (IL-6), soluble CD163 (sCD163),
D-dimer, T-cell and monocyte activation in the blood, and size of the HIV reservoir. 20
individuals will receive a single dose of 150mg canakinumab with follow-up for 18 weeks.
Inclusion Criteria:
1. HIV infection,
2. Age ≥ 40 years
3. On continuous ART for at least 12 months with no change in regimen in 12 weeks prior
to study entry
4. CD4+ T cell count ≥ 400 cells/mm3
5. HIV RNA level below the standard limit of quantification for 52 weeks prior to entry
6. High risk for CAD as defined by either documented CVD (including prior MI) or diabetes
mellitus or 1 CVD risk factor (current smoking, hypertension, dyslipidemia, or
hsCRP≥2mg/L.)
7. Individuals on stable doses of lipid lowering therapy, diabetes medication (not
including insulin) and/or anti-hypertensive medication will be allowed in the study.
8. Appropriate documentation from medical records of prior receipt of pneumococcal
vaccinations
Exclusion Criteria:
1. Women of childbearing potential or pregnant/nursing women
2. CABG surgery in the past 3 years
3. Class IV heart failure
4. Uncontrolled HTN or diabetes
5. History of tuberculosis or latent TB that is not treated
6. Nephrotic syndrome or eGFR< 30 ml/min/1.73m2
7. Active hepatic disease or active/chronic hepatitis B or C
8. Any prior malignancy including KS
9. Serious illness requiring hospitalization or active infection requiring antibiotics
within 90 days
10. Requirement for live active vaccination 3 months prior to, during, and 3 months after
study
11. Concurrent immune modulating therapy
12. Requirement for insulin
13. History of multiple imaging studies associated with radiation exposure
14. Neutropenia defined as ANC<1500/mm
15. Triglycerides>400 mg/dL
16. History of hypersensitivity to study drug
17. History of EBV-related lymphoproliferative disorders
18. Active or untreated latent TB infection
We found this trial at
2
sites
San Francisco, California 94115
Principal Investigator: Jay Lalezari, MD
Phone: 415-353-0212
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1001 Potrero Ave
San Francisco, California 94110
San Francisco, California 94110
(415) 206-8000
Principal Investigator: Priscilla Hsue, MD
Phone: 415-206-5801
San Francisco General Hospital San Francisco General Hospital and Trauma Center (SFGH) is an essential...
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