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Echo Therapeutics Announces Positive Results with the Prelude(TM) SkinPrep System, the Next-Generation Skin Permeation Medium for its Symphony(TM) Transdermal Continuous Glucose Monitoring System
Date:4/9/2008

data points fall within the A/B region, along with negligible or no D/E points. MARD is an error calculation tool that was used to measure the average relative difference between Symphony and the reference measurements, on a percentage basis. A low MARD error, below 20%, is generally accepted to be consistent with an accurate device.

Study Results

Using nearly 144 hours of continuous data from Symphony and 183 reference BG measurements from the 6 study subjects in a home use setting with self-administration, Clarke Error Grid analysis of the study data showed that Symphony had 100% of the data in the combined A and B regions with approximately 90% in the "A" region. No data points showed in the C, D and E regions. The MARD for the study was 9.0%. There were no Prelude or Symphony failures and no adverse events, indicating strong reliability of Prelude as the skin permeation medium for Symphony.

About Echo Therapeutics

Echo Therapeutics is focused on medical devices and specialty pharmaceuticals. Echo is developing a non-invasive, wireless, transdermal continuous glucose monitoring (tCGM) system for people with diabetes and for use in hospital critical care units, together with a wide range of novel transdermal reformulations of FDA-approved products.

Cautionary Statement Regarding Forward Looking Statements

Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any forward-looking statements contained herein are based on current expectations, but are subject to a number of risks and uncertainties. The factors that could cause actual future results to differ materially from current expectations include, but are not limited to, risks related to regulatory approvals and the success of Echo's ongoing studies regarding the efficacy of Echo's tCGM systems (including the Symphony
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SOURCE Echo Therapeutics
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