Spruce Biosciences, Inc. (NASDAQ:SPRB – Get Free Report) has earned an average rating of “Hold” from the eight research firms that are presently covering the firm, Marketbeat reports. Six research analysts have rated the stock with a hold recommendation and two have issued a buy recommendation on the company. The average 12-month price target among brokers that have issued a report on the stock in the last year is $5.00.
SPRB has been the topic of several recent research reports. HC Wainwright restated a “neutral” rating on shares of Spruce Biosciences in a research note on Monday, August 19th. Royal Bank of Canada restated a “sector perform” rating and issued a $2.00 price target on shares of Spruce Biosciences in a research note on Tuesday, August 13th.
Read Our Latest Stock Report on Spruce Biosciences
Institutional Trading of Spruce Biosciences
Spruce Biosciences Stock Up 1.0 %
Shares of NASDAQ:SPRB opened at $0.54 on Wednesday. Spruce Biosciences has a 52-week low of $0.41 and a 52-week high of $5.95. The firm has a market capitalization of $22.31 million, a P/E ratio of -0.52 and a beta of 2.36. The stock has a 50 day moving average price of $0.48 and a 200-day moving average price of $0.57. The company has a debt-to-equity ratio of 0.02, a quick ratio of 5.17 and a current ratio of 5.17.
Spruce Biosciences (NASDAQ:SPRB – Get Free Report) last posted its quarterly earnings results on Monday, August 12th. The company reported ($0.22) earnings per share for the quarter, topping the consensus estimate of ($0.32) by $0.10. The company had revenue of $1.61 million for the quarter, compared to the consensus estimate of $1.55 million. Spruce Biosciences had a negative return on equity of 59.94% and a negative net margin of 450.38%. As a group, equities research analysts anticipate that Spruce Biosciences will post -1.12 EPS for the current fiscal year.
About Spruce Biosciences
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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