Effect of IL--1β Inhibition on Inflammation and Cardiovascular Risk
Part of paid clinical trials in San Francisco, California.
- Sponsor
- Priscilla Hsue, MD
- Study ID
- NCT02272946
- Phase
- PHASE2
- Status
- Completed
Conditions
- Cardiovascular Disease
- HIV
Eligibility Criteria
- Sex
- ALL
- Age
- 40 Years - 59 Years
- Healthy Volunteers
- Not accepted
Interventions
- Canakinumab — DRUG150mg Canakinumab received subcutaneously
- Placebo — DRUG150mg Placebo received subcutaneously
Study Details
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. 10 individuals will receive a single dose of 150mg canakinumab with follow-up for 12 weeks. In the second part of the study, 100 participants will be randomized (2:1 - canakinumab to placebo) and will be followed by for 36 weeks.
Key Dates
- Start date
- Sep 30, 2015
- Status verified
- Mar 2023
- Primary completion
- Feb 28, 2021
- Completion
- Dec 31, 2021
Study Design
- Enrollment
- 43 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Other: Safety ArmIn Stage 1: all 10 subjects will receive 150 mg Canakinumab subcutaneous injection. This will be a preliminary safety study (before Stage II).
- Experimental: CanakinumabIn Stage II: About 67 subjects will receive 150mg Canakinumab subcutaneous injection.
- Placebo Comparator: PlaceboIn Stage II: About 33 subjects will receive 150mg placebo subcutaneous injection
Primary Outcome Measure
Change in CD4 Count From Baseline to Follow-up [ Time Frame: weeks 4, 8, 12, 18, 24, and 36. ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| San Francisco General Hospital | San Francisco | California | 94110 | - |
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