Larimar Therapeutics, Inc. (NASDAQ:LRMR – Get Free Report) has received an average recommendation of “Buy” from the twelve research firms that are covering the stock, Marketbeat reports. Eleven analysts have rated the stock with a buy recommendation and one has issued a strong buy recommendation on the company. The average 12 month price target among brokers that have covered the stock in the last year is $20.22.
LRMR has been the subject of a number of analyst reports. Truist Financial initiated coverage on shares of Larimar Therapeutics in a research note on Wednesday, January 29th. They issued a “buy” rating and a $18.00 target price for the company. HC Wainwright increased their target price on shares of Larimar Therapeutics from $15.00 to $16.00 and gave the stock a “buy” rating in a research report on Tuesday. Guggenheim reaffirmed a “buy” rating and issued a $26.00 price target on shares of Larimar Therapeutics in a research report on Tuesday. Finally, Robert W. Baird lowered their price objective on Larimar Therapeutics from $13.00 to $10.00 and set an “outperform” rating on the stock in a report on Tuesday.
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Institutional Investors Weigh In On Larimar Therapeutics
Larimar Therapeutics Trading Up 5.6 %
NASDAQ LRMR opened at $2.38 on Friday. Larimar Therapeutics has a 1-year low of $2.19 and a 1-year high of $11.20. The firm’s fifty day simple moving average is $3.10 and its 200-day simple moving average is $5.16. The company has a market capitalization of $151.54 million, a PE ratio of -2.07 and a beta of 0.99.
Larimar Therapeutics (NASDAQ:LRMR – Get Free Report) last issued its earnings results on Monday, March 24th. The company reported ($0.45) earnings per share for the quarter, missing the consensus estimate of ($0.29) by ($0.16). As a group, analysts predict that Larimar Therapeutics will post -1.15 EPS for the current year.
Larimar Therapeutics Company Profile
Larimar Therapeutics, Inc, a clinical-stage biotechnology company, focuses on developing treatments for rare diseases using its novel cell penetrating peptide technology platform. Its lead product candidate is CTI-1601, which is in Phase 2 OLE clinical trial for the treatment of Friedreich's ataxia, a rare, progressive and fatal genetic disease.
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