Fulcrum Therapeutics (NASDAQ:FULC – Get Free Report) will post its quarterly earnings results before the market opens on Monday, May 13th. Analysts expect Fulcrum Therapeutics to post earnings of ($0.44) per share for the quarter.
Fulcrum Therapeutics (NASDAQ:FULC – Get Free Report) last posted its quarterly earnings results on Tuesday, February 27th. The company reported ($0.40) earnings per share for the quarter, beating analysts’ consensus estimates of ($0.44) by $0.04. Fulcrum Therapeutics had a negative return on equity of 36.65% and a negative net margin of 3,470.05%. The company had revenue of $0.87 million for the quarter, compared to the consensus estimate of $0.65 million. On average, analysts expect Fulcrum Therapeutics to post $-2 EPS for the current fiscal year and $-2 EPS for the next fiscal year.
Fulcrum Therapeutics Stock Down 1.0 %
Shares of Fulcrum Therapeutics stock traded down $0.08 during trading on Tuesday, reaching $7.67. 100,712 shares of the company were exchanged, compared to its average volume of 610,850. Fulcrum Therapeutics has a twelve month low of $2.65 and a twelve month high of $13.70. The business has a 50-day moving average price of $9.05 and a 200-day moving average price of $7.15. The firm has a market capitalization of $476.69 million, a price-to-earnings ratio of -4.91 and a beta of 2.35.
Wall Street Analyst Weigh In
Read Our Latest Research Report on FULC
Insider Activity
In related news, VP Greg Tourangeau sold 4,884 shares of the stock in a transaction on Friday, March 8th. The shares were sold at an average price of $11.72, for a total transaction of $57,240.48. Following the completion of the transaction, the vice president now owns 11,807 shares in the company, valued at $138,378.04. The sale was disclosed in a filing with the Securities & Exchange Commission, which is accessible through the SEC website. 4.10% of the stock is owned by corporate insiders.
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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