Shares of Larimar Therapeutics, Inc. (NASDAQ:LRMR – Get Free Report) have received an average recommendation of “Buy” from the twelve analysts that are presently covering the firm, MarketBeat Ratings reports. Eleven research analysts have rated the stock with a buy rating and one has issued a strong buy rating on the company. The average 1-year target price among brokerages that have covered the stock in the last year is $20.22.
LRMR has been the topic of several analyst reports. HC Wainwright upped their price objective on Larimar Therapeutics from $15.00 to $16.00 and gave the company a “buy” rating in a research note on Tuesday. Guggenheim reiterated a “buy” rating and set a $26.00 price objective on shares of Larimar Therapeutics in a research note on Tuesday. Robert W. Baird cut their price objective on Larimar Therapeutics from $13.00 to $10.00 and set an “outperform” rating for the company in a report on Tuesday. Finally, Truist Financial started coverage on shares of Larimar Therapeutics in a report on Wednesday, January 29th. They issued a “buy” rating and a $18.00 target price on the stock.
View Our Latest Stock Analysis on Larimar Therapeutics
Hedge Funds Weigh In On Larimar Therapeutics
Larimar Therapeutics Price Performance
Shares of Larimar Therapeutics stock opened at $2.38 on Friday. Larimar Therapeutics has a 52-week low of $2.19 and a 52-week high of $11.20. The firm has a market capitalization of $151.54 million, a PE ratio of -2.07 and a beta of 0.99. The company’s fifty day moving average price is $3.10 and its two-hundred day moving average price is $5.16.
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). Analysts predict that Larimar Therapeutics will post -1.15 earnings per share for the current fiscal year.
About Larimar Therapeutics
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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