A Phase I/II, Single-Center, Randomized, Placebo-Controlled Study Evaluating the Therapeutic Efficacy of Intravenously Injected PEG-liposomal Prednisolone Sodium Phosphate (Nanocort®) in Subjects With Severe Inflamed Carotid or Aortic Atherosclerosis Plaques
Overview
- Phase
- Phase 1
- Intervention
- liposomal prednisolone
- Conditions
- Atherosclerosis
- Sponsor
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- 18Fludeoxyglucose Positron emission computed tomography scan (18FDG PET-CT scan)
- Last Updated
- 13 years ago
Overview
Brief Summary
Cardiovascular disease(CVD) is the leading cause of morbidity and mortality in developed nations. CVD is primarily caused by atherosclerosis, a systemic disease characterized by lipid deposition in the subendothelial space with a concomitant, low-grade inflammatory reaction.(Fuster, Moreno et al. 2005) To date, most therapeutic interventions aimed at lowering CVD have thus far focused on modulating lipid levels, either lowering LDLc or increasing HDLc levels. Yet, since the introduction of statins 20 years ago, there have been few breakthroughs in the treatment of this disease. A promising strategy to reduce CVD is to directly target inflammation at the level of the vessel wall.(van Leuven, van Wijk et al.; Libby 2002) A potential drawback of anti-inflammatory strategies pertains to the thin line between inhibiting 'inappropriate' inflammation versus inducing immuno-suppression. Therefore, continuous low dosed anti-inflammatory drugs have great potential as novel treatment strategies. In the present project, the investigators propose to inject liposomal glucocorticoids intravenously in patients with an increased risk of atherosclerotic disease aiming to reduce vessel wall inflammation.
Investigators
E.S.stroes
Professor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Eligibility Criteria
Inclusion Criteria
- •Population with target to background ratio of 2.2 of the aorta or carotid artery on PET-CT
Exclusion Criteria
- •Current medical history of auto-immune disease/vasculitis, active inflammatory diseases, Recent (\<1 month prior to screening) or ongoing serious infection requiring IV antibiotic therapy.
- •Recent or current treatment with medications that may have a significant effect on plaque inflammation as measured by plaque TBR, including but not limited to:
- •Steroids for at least 6 weeks prior to baseline measurement and during study (with the exception of inhaled acute use steroids).
- •Biological based medicines (anti-TNF (ex. Infliximab), anti-IL-6 therapy (ex. Tocilizumab) or anti-IL-1 (ex. anakinra)) within 8 weeks before the baseline visit and during the study
- •No other disease modifying antirheumatic drugs (DMRADS) within 6 weeks of baseline and during study (such as cyclosporine, azatioprine, etc.)
- •Known systemic disorders such as hepatic, renal, hematologic, and malignant diseases or any clinically significant medical condition that could interfere with the conduct of the study.
- •Changes in dose or frequency of doses at least 6 weeks prior to baseline measurement (unstable dosing) in angiotensin-converting enzyme (ACE) inhibitors (ACE-I) or angiotensin-receptor blockers (ARBs), non-statin lipid-modifying therapy, thiazolidinediones, inhaled steroids, or leukotriene modifying agents, nonsteroidal anti-inflammatory drugs (NSAIDS), and cyclo-oxygenase-2 inhibitors (COXIBs)
- •Standard contra-indications to MRI, 18FDG PET, and CT based on physicians experience and current practices
- •Current medical history of poorly controlled diabetes defined as hemoglobin A1c (HbA1c) \>7.5%.
- •Current medical history of drug or alcohol abuse within 12 months prior to screening.
Arms & Interventions
Liposomal prednisolone
Intervention: liposomal prednisolone
Placebo control
Intervention: liposomal prednisolone
Placebo control
Intervention: Placebo
Outcomes
Primary Outcomes
18Fludeoxyglucose Positron emission computed tomography scan (18FDG PET-CT scan)
Time Frame: Day 8-13