Synlogic, Inc. (NASDAQ:SYBX – Get Free Report) saw a large decrease in short interest in the month of January. As of January 15th, there was short interest totaling 7,729 shares, a decrease of 25.7% from the December 31st total of 10,406 shares. Currently, 0.1% of the company’s shares are short sold. Based on an average trading volume of 14,860 shares, the days-to-cover ratio is presently 0.5 days. Based on an average trading volume of 14,860 shares, the days-to-cover ratio is presently 0.5 days. Currently, 0.1% of the company’s shares are short sold.
Wall Street Analysts Forecast Growth
Separately, Weiss Ratings reiterated a “sell (e+)” rating on shares of Synlogic in a research report on Wednesday, October 8th. One analyst has rated the stock with a Sell rating, According to MarketBeat.com, the company currently has an average rating of “Sell”.
Read Our Latest Analysis on Synlogic
Hedge Funds Weigh In On Synlogic
Synlogic Price Performance
NASDAQ:SYBX opened at $0.63 on Monday. The firm’s fifty day simple moving average is $1.10 and its 200 day simple moving average is $1.42. The stock has a market cap of $7.37 million, a P/E ratio of -2.42 and a beta of 0.39. Synlogic has a twelve month low of $0.54 and a twelve month high of $1.96.
Synlogic (NASDAQ:SYBX – Get Free Report) last announced its earnings results on Thursday, November 13th. The biotechnology company reported ($0.19) earnings per share for the quarter, missing analysts’ consensus estimates of ($0.11) by ($0.08). On average, analysts expect that Synlogic will post -2.71 EPS for the current fiscal year.
About Synlogic
Synlogic, Inc, a clinical-stage biopharmaceutical company, engages in the discovery and development of synthetic biotics to treat metabolic diseases in the United States. Its pipeline include SYNB1618, an orally administered, non-systemically absorbed drug candidate to treat phenylketonuria; SYNB1934, an orally administered, non-systemically absorbed drug candidate, which is in Phase III clinical trial to treat phenylketonuria; SYNB1353, an orally administered, non-systemically absorbed drug candidate, which is in Phase I clinical to treat homocystinuria; SYNB8802, an orally administered, non-systemically absorbed drug candidate that is in Phase II clinical trial for the treatment of enteric hyperoxaluria; and SYNB2081 to lower uric acid for the potential treatment of gout.
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