Fulcrum Therapeutics, Inc. (NASDAQ:FULC – Get Free Report) has received an average rating of “Hold” from the ten research firms that are currently covering the firm, MarketBeat Ratings reports. One investment analyst has rated the stock with a sell rating, six have issued a hold rating and three have assigned a buy rating to the company. The average 12-month price target among brokers that have issued ratings on the stock in the last year is $9.33.
A number of equities research analysts have recently issued reports on FULC shares. Royal Bank of Canada reissued a “sector perform” rating and issued a $4.00 price target on shares of Fulcrum Therapeutics in a report on Thursday, November 14th. Leerink Partnrs downgraded shares of Fulcrum Therapeutics from a “strong-buy” rating to a “hold” rating in a research note on Thursday, September 12th. Bank of America downgraded shares of Fulcrum Therapeutics from a “neutral” rating to an “underperform” rating and lowered their target price for the company from $10.00 to $2.00 in a research note on Thursday, September 12th. Stifel Nicolaus downgraded shares of Fulcrum Therapeutics from a “buy” rating to a “hold” rating and lowered their target price for the company from $22.00 to $3.00 in a research note on Thursday, September 12th. Finally, Leerink Partners reaffirmed a “market perform” rating and issued a $4.00 target price on shares of Fulcrum Therapeutics in a research note on Thursday, September 12th.
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Fulcrum Therapeutics Trading Down 0.7 %
Shares of Fulcrum Therapeutics stock opened at $3.01 on Wednesday. Fulcrum Therapeutics has a 12-month low of $2.86 and a 12-month high of $13.70. The company has a market cap of $162.36 million, a price-to-earnings ratio of -9.71 and a beta of 2.24. The company’s 50-day moving average price is $3.53 and its 200-day moving average price is $6.40.
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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