drugset / Trial / NCT01201837

Effect of CER-001 on Atherosclerosis in Acute Coronary Syndrome (ACS) Patients - Efficacy and Safety: The CHI SQUARE Trial

NCT01201837 ↗

Phase 2 Completed 507 enrolled Cerenis Therapeutics, SA
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Cardiovascular disease remains the most pressing healthcare issue for developed countries and is becoming so for developing countries. There are a number of chronic therapies available for long-term management of risk. Short term therapies for subjects with an acute event, such as an episode of acute coronary syndrome (ACS), are focused on reperfusion and removing thrombus but most subsequent events are caused by atherosclerotic plaque rupture at a different site. There are no approved therapies that can rapidly reduce the burden of unstable, inflamed plaque in the overall coronary vascular bed. HDL has multiple actions that could lead to atherosclerotic plaque stabilization, such as rapid removal of large quantities of cholesterol from the vasculature, improvement in endothelial function, protection against oxidative damage and reduction in inflammation. This study will assess the effects of CER-001, an ApoA-I-based HDL mimetic, on indices of atherosclerotic plaque progression and regression as assessed by intravascular ultrasound (IVUS) measurements in patients with (ACS).

Timeline

Start
2011-03
Primary completion
2012-10
Completion
2013-03

Outcome

Missed primary endpoint

paper primary analysis of 12 mg/kg vs. placebo: P = 0.81 PMID 24780501 ↗

paper CER-001 infusions did not reduce coronary atherosclerosis on IVUS and QCA when compared with placebo. PMID 24780501 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CER-001 Protein / enzyme biologic 3 mg/kg —
Subject CER-001 Protein / enzyme biologic 6 mg/kg —
Subject CER-001 Protein / enzyme biologic 12 mg/kg —