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VYVANSE CII Provided Significant Efficacy At 14 Hours After Administration In Adults With ADHD In An Adult Simulated Workplace Environment
Shire plc (LSE: SHP, NASDAQ: SHPGY), the global specialty biopharmaceutical company, announced results from a Phase 3b study that found VYVANSE® (lisdexamfetamine dimesylate) CII demonstrated significant efficacy at 14 hours after administration during a simulated workplace environment study in adults with Attention Deficit Hyperactivity Disorder (ADHD). VYVANSE is the first approved stimulant for adults with ADHD to be evaluated in this setting, and these data were presented today at the 49th annual New Clinical Drug Evaluation Unit meeting in Hollywood, FL. VYVANSE is currently approved by the US Food and Drug Administration (FDA) for the treatment of ADHD in children age 6 to 12 years and in adults with ADHD.
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Probiotics Can Increase Effectiveness Of Some Antibiotic Therapies For Bacterial Vaginosis
Antimicrobial treatments for bacterial vaginosis (BV) are effective, but taking lactobacillus tablets alongside metronidazole antibiotic therapy increases effectiveness over taking this antibiotic alone, according to a Cochrane Systematic Review. The researchers also concluded that intravaginal lactobacillus was as effective as oral metronidazole, although they did note unexplained drop-outs from the trials.
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First Mosquitoes Test Positive For West Nile Virus In Southern Illinois
Dr. Damon T. Arnold, state public health director, announced a mosquito batch collected in St. Clair County has been confirmed as the first positive West Nile virus test results in southern Illinois this year.
Diagnostics

Seegene's Seeplex(R) RV Multiplex PCR Tests Prove Effective For The Identification Of The New Influenza A H1N1

Building on its widely distributed multiplex PCR technology platform, Seegene is now providing healthcare systems worldwide with a powerful diagnostic test for effective identification of the new influenza A virus (swine H1N1). The Seeplex® RV Detection* assays provide a wide range of screening capabilities for Influenza A, while simultaneously testing for up to 18 other respiratory viruses in a single multiplex PCR test. During this current influenza A outbreak, Seegene"s RV products using the company"s sequencing primer patch for final confirmation of swine H1N1 are in use by approximately 200 hospitals worldwide including Mexico, Spain and Korea. In a recent direct comparison of commercially available diagnostic tests, Seegene"s multiplex PCR technology returned the best results for screening for new influenza A virus in a trial conducted by the Ontario Agency for Health Protection and Promotion. The Seeplex RV12 ACE Detection with H1N1 primer patch showed 100% specificity and 95% sensitivity in testing for Swine-origin influenza virus (SOIV) in nasopharyngeal specimens. Seegene offers its supplemental H1N1 specific primer in all respiratory virus detection products while the current H1N1 outbreak lasts. By using this additional primer, any suspicious sample can be checked by two-way detecting process -- first detection by Influenza A conserved matrix (M) gene primer, then subsequent or simultaneous detection by new H1N1 specific hemagglutinin (H) gene primer. While the H1N1 virus has been identified as a pandemic strain, healthcare systems around the world do not yet know what impact this pathogen and its variants will have as the regular flu season approaches, and are therefore seeking reliable screening tools to rapidly expand testing capacity. To help prepare health systems for a robust response in the upcoming flu season, Seegene will release a dedicated multiplex PCR test for Flu A sub-typing in September, which is capable of simultaneously detecting the most common subtypes (H1, H3 and H5) seen in the current and past outbreaks. This test will also provide useful information for the proper antiviral drug prescription as there are many reports about antiviral drug resistance in each serotype. * Seeplex RV Detection tests are for research use in US. Seegene


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