Spruce Biosciences, Inc. (NASDAQ:SPRB – Get Free Report) has earned an average recommendation of “Hold” from the eight brokerages that are presently covering the stock, MarketBeat reports. Six research analysts have rated the stock with a hold recommendation and two have given a buy recommendation to the company. The average 12 month target price among brokerages that have issued a report on the stock in the last year is $4.00.
Several equities analysts have issued reports on SPRB shares. HC Wainwright reaffirmed a “neutral” rating on shares of Spruce Biosciences in a report on Monday, August 19th. Royal Bank of Canada reaffirmed a “sector perform” rating and issued a $2.00 price target on shares of Spruce Biosciences in a research note on Tuesday, November 12th.
View Our Latest Analysis on SPRB
Hedge Funds Weigh In On Spruce Biosciences
Spruce Biosciences Price Performance
Shares of Spruce Biosciences stock opened at $0.50 on Friday. The firm has a market cap of $20.64 million, a PE ratio of -0.53 and a beta of 2.34. Spruce Biosciences has a twelve month low of $0.41 and a twelve month high of $5.95. The company has a quick ratio of 5.36, a current ratio of 5.36 and a debt-to-equity ratio of 0.01. The business has a 50-day moving average price of $0.51 and a 200 day moving average price of $0.53.
Spruce Biosciences (NASDAQ:SPRB – Get Free Report) last posted its quarterly earnings data on Monday, November 11th. The company reported ($0.21) EPS for the quarter, beating analysts’ consensus estimates of ($0.27) by $0.06. Spruce Biosciences had a negative return on equity of 62.10% and a negative net margin of 555.23%. The business had revenue of $0.60 million during the quarter, compared to analysts’ expectations of $1.80 million. Sell-side analysts predict that Spruce Biosciences will post -1.03 earnings per share for the current fiscal year.
Spruce Biosciences Company Profile
Spruce Biosciences, Inc, a biopharmaceutical company, focuses on developing and commercializing novel therapies for rare endocrine disorders. The company engages in developing tildacerfont, a non-steroidal therapy to enhance disease control and reduce steroid burden for patients suffering from congenital adrenal hyperplasia (CAH), which is in Phase 2b clinical trial; and to evaluate glucocorticoid reduction in adult patients with classic CAH that is Phase 2b clinical trial.
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