Shares of Spruce Biosciences, Inc. (NASDAQ:SPRB – Get Free Report) have earned an average rating of “Hold” from the six brokerages that are covering the company, Marketbeat reports. Six equities research analysts have rated the stock with a hold rating. The average twelve-month target price among analysts that have issued a report on the stock in the last year is $2.17.
Separately, Royal Bank of Canada cut their target price on shares of Spruce Biosciences from $1.50 to $0.50 and set a “sector perform” rating for the company in a research note on Wednesday, April 16th.
Check Out Our Latest Analysis on SPRB
Spruce Biosciences Price Performance
Spruce Biosciences (NASDAQ:SPRB – Get Free Report) last released its quarterly earnings data on Tuesday, April 15th. The company reported ($0.57) EPS for the quarter, missing analysts’ consensus estimates of ($0.20) by ($0.37). The business had revenue of $0.55 million for the quarter, compared to the consensus estimate of $0.50 million. Spruce Biosciences had a negative return on equity of 62.10% and a negative net margin of 555.23%. Analysts expect that Spruce Biosciences will post -1 EPS for the current year.
Institutional Investors Weigh In On Spruce Biosciences
An institutional investor recently bought a new position in Spruce Biosciences stock. Boothbay Fund Management LLC purchased a new stake in Spruce Biosciences, Inc. (NASDAQ:SPRB – Free Report) during the 4th quarter, according to its most recent Form 13F filing with the SEC. The institutional investor purchased 288,800 shares of the company’s stock, valued at approximately $121,000. Boothbay Fund Management LLC owned 0.70% of Spruce Biosciences as of its most recent SEC filing. Institutional investors own 91.71% of the company’s stock.
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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