Larimar Therapeutics, Inc. (NASDAQ:LRMR – Get Free Report) has earned a consensus rating of “Buy” from the twelve research firms that are currently covering the stock, MarketBeat reports. Eleven equities research analysts have rated the stock with a buy recommendation and one has given a strong buy recommendation to the company. The average 1-year price objective among brokers that have issued a report on the stock in the last year is $20.13.
Several research analysts have weighed in on LRMR shares. William Blair reiterated an “outperform” rating on shares of Larimar Therapeutics in a research note on Tuesday, November 19th. Oppenheimer began coverage on shares of Larimar Therapeutics in a research note on Wednesday, October 16th. They issued an “outperform” rating and a $26.00 price objective on the stock. Truist Financial initiated coverage on shares of Larimar Therapeutics in a research note on Wednesday. They issued a “buy” rating and a $18.00 target price for the company. Finally, HC Wainwright reiterated a “buy” rating and set a $15.00 price target on shares of Larimar Therapeutics in a research note on Friday, January 24th.
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Larimar Therapeutics Price Performance
Shares of NASDAQ:LRMR opened at $3.84 on Friday. Larimar Therapeutics has a 1-year low of $3.01 and a 1-year high of $13.68. The stock has a market cap of $245.02 million, a P/E ratio of -3.34 and a beta of 0.91. The firm has a fifty day moving average price of $4.60 and a 200 day moving average price of $6.65.
Larimar Therapeutics (NASDAQ:LRMR – Get Free Report) last announced its earnings results on Wednesday, October 30th. The company reported ($0.24) earnings per share for the quarter, topping the consensus estimate of ($0.37) by $0.13. During the same quarter last year, the company posted ($0.21) EPS. Sell-side analysts expect that Larimar Therapeutics will post -1.15 EPS for the current fiscal 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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