The NuroPro AD test was developed to help clinicians diagnose patients with Alzheimer's, as well as to distinguish those with Alzheimer's from normal individuals and patients with other neurological disorders. The NuroPro test, developed by Power3, utilizes a panel of blood serum protein biomarkers to determine the probability that a patient has Alzheimer's. The tests are intended to solve a critical challenge facing physicians, clinicians, and patients toward an objective, early stage and accurate diagnosis of actual disease.
"In the US, there are an estimated 5.1 million individuals with Alzheimer's disease," said Power3's President and Chief Scientific Officer, Dr. Ira L. Goldknopf. "The annual treatment per patient is currently in excess of $30 thousand for Alzheimer's."
Power3 is conducting the independent validation of both their Alzheimer's (NuroPro AD) and Parkinson's (NuroPro PD) tests with key clinical centers. The second phase of these prospective trials, as well as the launch of the CLIA-certified testing services, are both slated to commence sometime in late 2009.
According to Helen R. Park, CEO of Power3, "Progress thus far of the Company's clinical validation trials confirms our belief that Power3's NuroPro AD will significantly help physicians make diagnoses and recommend appropriate follow-up and treatment options for their patients, based on the presence of disease. This is a huge advance over only being capable of informing a patient that his or her risk is high."
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About Power3 Medical Products, Inc
Power3 Medical Products (OTC BB:PWRM.OB) (www.power3medical.com)
Power3 expects to complete phase II clinical validation trials of its blood serum diagnostics for Alzheimer's and Parkinson's disease (NuroPro AD and PD), in the fourth quarter of 2009, followed by completion of filing with the FDA. Power3 operates a state-of-the-
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Source: Power3 Medical Products, Inc.
