News coverage about Auris Medical (NASDAQ:EARS) has been trending somewhat positive this week, according to Accern Sentiment Analysis. The research group ranks the sentiment of media coverage by monitoring more than 20 million news and blog sources in real-time. Accern ranks coverage of public companies on a scale of -1 to 1, with scores closest to one being the most favorable. Auris Medical earned a media sentiment score of 0.15 on Accern’s scale. Accern also assigned news headlines about the biotechnology company an impact score of 47.5203753227658 out of 100, indicating that recent media coverage is somewhat unlikely to have an effect on the company’s share price in the near future.
Here are some of the headlines that may have effected Accern Sentiment’s rankings:
- Auris Medical Holding AG (EARS) : Investors watching Analysts Rating – Wall Street Morning (wallstreetmorning.com)
- Global Vertigo Market: Industry Analysis & Outlook 2017-2021: Major Players are Auris Medical, Sensorion, Otonomy and Sound Pharmaceuticals – Research and Markets (businesswire.com)
- Auris Medical Holding AG (NASDAQ:EARS) Announces Positive Results From Phase III Trial Of Am-111 For Treatment … – USMarketsDaily (blog) (usmarketsdaily.com)
- Global Vertigo Market Competition by Manufacturers Opportunities and Forecast to 2021 (medgadget.com)
Shares of Auris Medical (EARS) traded up $0.02 during midday trading on Monday, reaching $0.50. The company’s stock had a trading volume of 2,538,500 shares, compared to its average volume of 501,236. The company has a current ratio of 1.86, a quick ratio of 1.86 and a debt-to-equity ratio of -14.04. The company has a market cap of $24.33, a price-to-earnings ratio of -0.78 and a beta of 0.59. Auris Medical has a 52-week low of $0.38 and a 52-week high of $1.39.
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Auris Medical Company Profile
Auris Medical Holding AG is a holding and clinical-stage biopharmaceutical company focused on the development of products for the treatment of inner ear disorders. Its advanced product candidate, AM-101, is in Phase III clinical development for acute inner ear tinnitus under a special protocol assessment (SPA) from the United States Food and Drug Administration.
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