Fulcrum Therapeutics, Inc. (NASDAQ:FULC – Get Free Report) has been assigned a consensus recommendation of “Hold” from the nine ratings firms that are covering the firm, MarketBeat.com reports. One investment analyst has rated the stock with a sell recommendation, six have given a hold recommendation and two have issued a buy recommendation on the company. The average 1-year price objective among brokerages that have covered the stock in the last year is $8.63.
A number of equities analysts have weighed in on the company. HC Wainwright reaffirmed a “neutral” rating and set a $4.00 price target on shares of Fulcrum Therapeutics in a research report on Wednesday, February 26th. Royal Bank of Canada restated a “sector perform” rating and set a $4.00 target price on shares of Fulcrum Therapeutics in a report on Thursday, November 14th.
Read Our Latest Analysis on Fulcrum Therapeutics
Institutional Inflows and Outflows
Fulcrum Therapeutics Stock Down 0.9 %
Shares of NASDAQ:FULC opened at $3.22 on Friday. The firm has a market cap of $173.81 million, a price-to-earnings ratio of -10.39 and a beta of 2.20. Fulcrum Therapeutics has a 12 month low of $2.86 and a 12 month high of $12.40. The company’s fifty day simple moving average is $3.99 and its 200 day simple moving average is $4.40.
Fulcrum Therapeutics (NASDAQ:FULC – Get Free Report) last issued its quarterly earnings results on Tuesday, February 25th. The company reported ($0.31) EPS for the quarter, missing analysts’ consensus estimates of ($0.28) by ($0.03). Research analysts expect that Fulcrum Therapeutics will post -0.16 earnings per share for the current fiscal year.
Fulcrum Therapeutics Company Profile
Fulcrum Therapeutics, Inc, a clinical-stage biopharmaceutical company, focuses on developing products for improving the lives of patients with genetically defined diseases in the areas of high unmet medical need in the United States. Its product candidates are losmapimod, a small molecule for the treatment of facioscapulohumeral muscular dystrophy is under phase III clinical trial; and pociredir, a fetal hemoglobin inducer for the treatment of sickle cell disease and beta-thalassemia is under phase I clinical trial.
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