Nour Heart is a Connecticut-based biomedical company aimed at developing diagnostic and therapeutic products for the early detection, prevention, and treatment of myocardial ischemia in patients with ischemic heart disease.
Nour Heart is currently developing and commercializing for human use its innovative and patented technologies related to Nourin molecular biomarkers for myocardial ischemia and the cardioprotective, Nourexal (Cyclocreatine Phosphate).
Nourin®miRNAs: Novel Molecular Biomarkers to Rule-in or Rule-out Early Myocardial Ischemia in Chest Pain Patients Suspected of Having Unstable Angina (UA) or Stable Coronary Artery Disease (SCAD) before Progressing to Infarction (Necrosis), with Particular Benefits for Women.
Read More ...Nourexal® (Cyclocreatine Phosphate): A Novel Preventive Bioenergetic / Anti-inflammatory Therapy to Protect Hearts Against Ischemic Injury and Restore Cardiac Function with Clinical Applications in Heart Transplantation, Cardiac Surgery, and Interventional Cardiology.
Read More ...Dr. Elgebaly is a Cardio Pharmacologist who founded Nour Heart, Inc. in Hartford, Connecticut, U.S. and she is the Company’s Chief Executive Officer (CEO). The Company’s mission is to develop and commercialize diagnostic and therapeutic products for the early detection, prevention, and treatment of myocardial ischemia in patients with ischemic heart disease. She is a former Associate Professor and Director of Surgical Research at the Department of Surgery, University of Connecticut School of Medicine, Farmington, Connecticut, U.S. Currently Dr. Elgebaly holds an adjunct faculty position at the Department of Surgery, University of Connecticut School of Medicine.
Read MoreOur team has extensive experience in drug development and commercialization according to USFDA regulations. Nour Heart’s team includes cardiac pharmacologists, cardiac surgeon, transplant surgeon, intervention cardiologist, non-invasive cardiologist, experts in cardiac biomarkers (protein and molecular), drug process chemistry, formulation, and manufacturing according to FDA Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP), as well as extensive expertise in Active Pharmaceutical Ingredient (API) and finished product manufacturing, validation, Quality Assurance (QA), Investigational New Drug (IND) application and New Drug Application (NDA) filings to the USFDA.
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