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Aposcience - Pre-Clinical
The company`s systemic formulation (APO-1 (APOSECTM)) derived from peripheral white blood cells (PBMCs) has been evaluated in animal models of wound healing, stroke, spinal cord injury, and models of chronic and acute myocardial infarction.
Peripheral White Blood Cells (PBMCs)
PBMCs driven into apoptosis through cellular stress have been shown to be highly potent in experimental wound healing, stroke, spinal cord injury, acute and chronic infarction models and prevention of ischemia reperfusion injury.
Pre-Clinical
The company`s systemic formulation (APO-1 (APOSECTM)) derived from peripheral white blood cells (PBMCs) has been evaluated in animal models of wound healing, stroke, spinal cord injury, and models of chronic and acute myocardial infarction.
Aposcience - Focus Wound Healing
Aposcience - Focus Myocardial Infarction
Aposcience AG has identified APO-1 (APOSECTM), derived from the secretome of irradiated, apoptotic peripheral blood mononuclear cells (PBMCs) as superbly efficacious in reducing infarct size and maintaining left ventricular function in animal models of myocardial infarction (MI). These models tested MI with and without reperfusion, including one of ischemia and reperfusion. These data are predictive for the prevention of adverse remodeling following revascularization of an acute MI. The target population are those over 700,000 patients worldwide who undergo reperfusion treatment for acute ST-elevation myocardial infarction. If APO-1 (APOSECTM) proves effective in clinical trials, the market potential is estimated at 1 – 2 billion Euros annually.
Clinical
APOSEC - Model APO-1 - Injectable formulation for the improvement of cardiac function in chronic myocardial ischemia
Discussions are underway for the design of a clinical program in this indication together with a manufacturer of catheter devices suitable for direct myocardial injection of APO-1 (APOSECTM)
APOSEC - Model APO-2 - Topical formulation for the treatment of diabetic foot ulcers and other chronic wounds
Aposcience AG will initiate a program to demonstrate safety and efficacy in this important indication with very large unmet medical need. The program consists of a phase I study in healthy volunteers, followed by a phase IIa study in a selected patient population. This program is designed to translate the extremely promising data from animal models into clinical practice.
