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Nanomix Corp NNMX

Nanomix Corporation is engaged in development of mobile point-of-care diagnostics. The Company operates through its Nanomix eLab System platform and assays that provide quantitative information for use in settings where time is critical to clinical decision-making and improved patient care. The platform is designed to provide rapid test results in a handheld device at the first point of patient contact in locations that range from emergency departments to long term and assisted care facilities, to urgent care and emergency medical response settings. Its platform is performed in a range of in vitro diagnostic assays, such as electrochemical immunoassay and enzymatic assays. Its eLab System utilizes a nano-biosensor with multiple detection electrodes to generate multiple electrochemical assay results. Its S1 Assay panel is used as an aid in diagnosing infections, such as sepsis. Its CRP test results can be used to evaluate infection, tissue injury, and inflammatory disorders.


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Post by MissionIRon Jan 21, 2014 6:39pm
255 Views
Post# 22118025

Boston Therapeutics, Inc. (BTHE) Prepares for Third Phase Tr

Boston Therapeutics, Inc. (BTHE) Prepares for Third Phase Tr

Boston Therapeutics, Inc. (BTHE) Prepares for Third Phase Trial of PAZ320

Boston Therapeutics is a pharmaceutical company focused on the development, manufacturing, and commercialization of novel compounds based on complex carbohydrate chemistry to address unmet medical needs in diabetes.

PAZ320 is an integral part of the company’s initial product pipeline, which is focused on developing and commercializing therapeutic molecules. PAZ320 is a non-systemic, non-toxic, chewable drug which inhibits the enzymes that release glucose from complex carbohydrates in foods during digestion, reducing the amount of available glucose absorbed through the intestine.

In November, Boston Therapeutics enrolled 24 patients with Type 2 diabetes in a Phase IIb clinical study on PAZ320, and positive results from the trial were published by the principal investigator in the July/August issue of the journal “Endocrine Practice”. After evaluating the safety and efficacy of PAZ320, it was shown that there was a significant 40% reduction in elevation of post-meal blood glucose in the participating patients, with no serious adverse events.

By the second or third quarter of 2014, the company hopes to begin an important Phase III trial of the chewable tablet it is promoting as a potential adjunct to metformin in patients living with Type 2 diabetes. While the Phase IIb trial was held only in France, the Phase III trial will be multi-national–in the United States, Europe, Hong Kong, and China.

The company believes that PAZ320 is a safe and effective drug compound for people with pre-diabetes and diabetes in their daily management of blood glucose levels, fulfilling an unmet medical need. The intent is for this compound to provide individuals with a means by which to slow the onset of Type 2 diabetes and/or the onset of diabetes complications such as heart disease, stroke, kidney damage, retinopathy, and Diabetic Foot.

PAZ320 is meant to be taken before meals and works in the gastrointestinal tract to block the action of carbohydrate-hydrolyzing enzymes that break down complex carbohydrates into simple sugars, reducing the availability of glucose for absorption into the bloodstream.

For more information about PAZ320 or any of the company’s other products, visit the website at www.bostonti.com

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