NeuroVive Pharmaceutical AB (publ), the mitochondrial medicine company, reports that the phase III CIRCUS study of CicloMulsion in patients with a specific type of heart attack known as ST-segment elevation acute myocardial infarction (STEMI) did not meet its primary clinical endpoint in a topline analysis.
The topline analysis of the study data provides information on whether the primary endpoint has been met or not. This result does not contain specific data concerning the level of significance for either the composite endpoint or each individual element of the composite endpoint. These will be revealed in the subsequent detailed analysis. It is anticipated that the full results of the 12-month data from the CIRCUS study will be made available in the third quarter. Today’s topline result is expected to delay the commercialization of CicloMulsion.
“While the primary endpoint of the CIRCUS study has not been met, analysis of the full 12-month data set will provide us with more information in regard to which patients may have benefited from treatment with CicloMulsion. These results will help define next steps in the development and commercialization of CicloMulsion. The CIRCUS study is an independent, investigator-led study and we will continue to collaborate with the lead investigator to further evaluate the full 12-month study results as they become available,” commented NeuroVive’s CEO Mikael Brönnegård.
"We are confident in the NeuroVive R&D pipeline and the potential of cyclophilin inhibitors including CicloMulsion. CicloMulsion is one of several products and projects in clinical and preclinical stages including the ongoing phase II CiPRICS and CHIC studies. Our continuing clinical programme coupled with a strong research and development pipeline will support NeuroVive’s future growth,” he added.
The primary endpoint is a composite of three separate outcomes: mortality, hospitalization for heart failure and left-ventricular (LV) remodelling at 12 months post acute myocardial infarction. The primary objective of the study was to determine whether CicloMulsion can improve STEMI patient clinical outcomes 12 months after administration. CicloMulsion or placebo was administered directly prior to percutaneous coronary intervention (PCI), a common procedure to reopen the coronary artery allowing the return of blood flow to the heart. The study will continue for a further two years to investigate longer term outcomes. CicloMulsion is an investigational product and has not been approved by regulatory agencies for the treatment of any medical condition.
The impact of the CIRCUS results on the future development of CicloMulsion will be communicated in the second half of 2015.
Acute myocardial infarction (AMI), commonly known as heart attack, is caused by blockage of a coronary artery obstructing blood flow to the tissue of the heart, which results in cell damage or death (infarct) leading to reduced heart function, heart failure and possible death. STEMI is a diagnostic classification of more severe myocardial infarction in which the damage to the cardiac muscle, caused by complete coronary artery blockage, is first detected by electrocardiography (ECG).
The CIRCUS study (does Cyclosporine ImpRove Clinical oUtcome in ST elevation myocardial infarction patients) is an ongoing phase III study assessing CicloMulsion® in 975 patients undergoing PCI following STEMI to assess its ability to protect cardiac tissue and improve clinical outcomes.
The study is a multicentre, randomized, placebo-controlled, double-blind, investigator-initiated study. Patients received one intravenous dose of CicloMulsion (or placebo) prior to reperfusion therapy by PCI. The incidence of the combined endpoint (mortality, hospitalization for heart failure, LV remodeling) will be assessed at 12 months after treatment to determine whether CicloMulsion can improve the clinical outcome in STEMI patients. The study also includes a number of secondary outcome measures designed to provide a more detailed insight into CicloMulsion's ability to reduce a patient's level of cardiac injury following PCI. There will also be further analyses at 36 months after treatment to discover longer term effects of CicloMulsion.
The trial is being led by Professor Michel Ovize, MD, PhD, of Hospices Civils de Lyon (HCL), a leading expert in the field of cardiovascular medicine and it is conducted by a clinical research organization (CRO) unit according to good clinical practice (GCP) guidelines. The study has enrolled patients at centres in France, Belgium and Spain. The CIRCUS trial is an investigator-initiated trial that is supported by a national PHRC program funded by the French Ministry of Health (PHRC National 2010). Furthermore, it is supported by grants from NeuroVive Pharmaceutical AB, Lund, Sweden, that also provides the study treatment CicloMulsion and matching placebo.
NeuroVive’s drug candidate CicloMulsion, a cremophor-free lipid emulsion formulation of cyclosporine, is the first cyclophilin inhibitor in development for the treatment of reperfusion injury. It is designed to prevent mitochondria dysfunction in damaged cells and limit the numerous biochemical processes that lead to secondary tissue damage. By protecting the mitochondria, CicloMulsion may safeguard continued energy production and ensure that the normal healing process is able to carry out repairs and maintain cell functionality. CicloMulsion’s potential for treatment in connection with STEMI is currently being evaluated in a clinical phase III study. CicloMulsion is also being evaluated in a phase II study for the prevention of renal injury during major heart surgery with Skåne University Hospital in Lund, Sweden. CicloMulsion is an investigational product and has not been approved by regulatory agencies for the treatment of any medical condition.