Spruce Biosciences, Inc. (NASDAQ:SPRB - Free Report) - Analysts at Leerink Partnrs cut their FY2025 earnings per share estimates for shares of Spruce Biosciences in a research note issued on Tuesday, October 21st. Leerink Partnrs analyst J. Schwartz now anticipates that the company will post earnings of ($2.96) per share for the year, down from their prior estimate of ($2.83). The consensus estimate for Spruce Biosciences' current full-year earnings is ($1.00) per share. Leerink Partnrs also issued estimates for Spruce Biosciences' Q4 2025 earnings at ($6.85) EPS, Q1 2026 earnings at ($7.13) EPS, Q2 2026 earnings at ($7.43) EPS, Q3 2026 earnings at ($7.75) EPS, Q4 2026 earnings at ($8.07) EPS, FY2026 earnings at ($30.38) EPS and FY2027 earnings at ($38.56) EPS.
A number of other brokerages have also recently issued reports on SPRB. Weiss Ratings reaffirmed a "sell (d-)" rating on shares of Spruce Biosciences in a report on Tuesday, October 14th. Leerink Partners set a $160.00 target price on Spruce Biosciences and gave the stock a "market perform" rating in a report on Tuesday. Finally, Zacks Research raised Spruce Biosciences from a "hold" rating to a "strong-buy" rating in a report on Thursday, October 16th. One research analyst has rated the stock with a Strong Buy rating, seven have given a Hold rating and one has issued a Sell rating to the company. According to data from MarketBeat, Spruce Biosciences presently has a consensus rating of "Hold" and a consensus price target of $140.83.
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Spruce Biosciences Stock Performance
Spruce Biosciences stock opened at $129.92 on Friday. Spruce Biosciences has a 52 week low of $4.28 and a 52 week high of $240.00. The stock has a fifty day moving average of $49.79 and a 200-day moving average of $22.59. The stock has a market capitalization of $72.76 million, a P/E ratio of -1.51 and a beta of 2.47.
Spruce Biosciences Company Profile
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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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