Astria Therapeutics, Inc. (NASDAQ:ATXS – Get Free Report) saw a large decline in short interest in the month of December. As of December 15th, there was short interest totalling 2,680,000 shares, a decline of 14.9% from the November 30th total of 3,150,000 shares. Based on an average trading volume of 329,100 shares, the days-to-cover ratio is currently 8.1 days. Approximately 5.6% of the shares of the company are short sold.
Analysts Set New Price Targets
ATXS has been the subject of several recent analyst reports. HC Wainwright reiterated a “buy” rating and issued a $16.00 price objective on shares of Astria Therapeutics in a report on Tuesday, December 10th. Oppenheimer lifted their price target on Astria Therapeutics from $26.00 to $28.00 and gave the company an “outperform” rating in a research report on Thursday, November 14th. Five investment analysts have rated the stock with a buy rating and one has assigned a strong buy rating to the company. Based on data from MarketBeat.com, Astria Therapeutics currently has an average rating of “Buy” and an average price target of $25.60.
Check Out Our Latest Research Report on ATXS
Institutional Investors Weigh In On Astria Therapeutics
Astria Therapeutics Stock Performance
Shares of NASDAQ:ATXS traded down $0.03 during midday trading on Tuesday, reaching $8.85. The company had a trading volume of 69,863 shares, compared to its average volume of 583,023. The company has a fifty day simple moving average of $10.40 and a two-hundred day simple moving average of $10.73. The firm has a market cap of $499.44 million, a price-to-earnings ratio of -4.23 and a beta of 0.67. Astria Therapeutics has a 1-year low of $6.58 and a 1-year high of $16.90.
Astria Therapeutics Company Profile
Astria Therapeutics, Inc, a biopharmaceutical company, focuses on the discovery, development, and commercialization of therapeutics for allergic and immunological diseases in the United States. Its lead product candidate is STAR-0215, a monoclonal antibody inhibitor of plasma kallikrein, which is in Phase 1b/2 clinical trials for the treatment of hereditary angioedema.
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