A Study to Evaluate the Safety, Tolerability, and Activity of Intravenous MLDL1278A in Patients on Standard-of-Care Therapy for Stable Atherosclerotic Cardiovascular Disease (GLACIER)
Status: | Completed |
---|---|
Conditions: | Peripheral Vascular Disease, Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 35 - 80 |
Updated: | 4/21/2016 |
Start Date: | March 2010 |
A Multicenter, Randomized, Double Blind, Placebo-Controlled Phase II Study to Evaluate the Safety, Tolerability, and Activity of Intravenous MLDL1278A in Patients on Standard-of-Care Therapy for Stable Atherosclerotic Cardiovascular Disease (GLACIER - Goal of Oxidized Ldl and Activated Macrophage Inhibition by Exposure to a Recombinant Antibody)
This is a Phase II (proof-of-activity), double-blind, placebo-controlled, randomized,
multicenter study of MLDL1278A (also known as BI-204) involving patients on standard-of-care
therapy for atherosclerotic cardiovascular disease with evidence of vascular inflammation,
as quantified by FDG-PET/CT.
multicenter study of MLDL1278A (also known as BI-204) involving patients on standard-of-care
therapy for atherosclerotic cardiovascular disease with evidence of vascular inflammation,
as quantified by FDG-PET/CT.
Inclusion Criteria:
- Evidence of qualifying vessel (carotid or aortic) plaque inflammation
- Documented atherosclerotic vascular disease clinically stable for at least 3 months
prior to screening or type 2 diabetes mellitus with elevated cardiovascular risk
- Use of a stable dose of statin therapy for at least 6 weeks prior to screening.
Patients must be capable of maintaining statin therapy at a current dose level from
screening until the last follow-up visit.
- For patients taking angiotensin-converting enzyme (ACE) inhibitors (ACE-I) or
angiotensin-receptor blockers (ARBs), non-statin lipid-modifying therapy,
thiazolidinediones, inhaled steroids, or leukotriene modifying agents, use of a
stable dose for at least 6 weeks prior to screening and capable of continuing with
that dose for the duration of the study
Exclusion Criteria:
- Occurrence of a cardiovascular event < 6 months prior to screening
- Pregnant, planning to become pregnant during the study, or breastfeeding
- Clinically significant abnormal laboratory values or abnormal ECG or vital signs
- History of anaphylactic reactions
- Newly discovered Type 2 diabetes mellitus (T2DM) (prior to study entry) or medical
treatment for T2DM started < 3 months prior to study entry
- Use of insulin, corticosteroids (oral, rectal, or injectable), or other
immunosuppressive medications
- Current or recent (within 4 weeks prior to screening) infection, including signs,
symptoms or serology of any infection, including HIV, hepatitis B or C
- Impaired renal function
- History of malignancy within 2 years prior to screening
- Current life-threatening condition other than vascular disease that may prevent a
patient from completing the study
- Use of an investigational drug or biologic within 30 days or 5 half-lives (whichever
is longer) prior to the first dose of study medication
- Exposure to substantial radiation within 12 months prior to screening
We found this trial at
19
sites
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