Shares of Larimar Therapeutics, Inc. (NASDAQ:LRMR – Get Free Report) have received a consensus recommendation of “Buy” from the nine brokerages that are currently covering the stock, Marketbeat Ratings reports. Eight equities research analysts have rated the stock with a buy rating and one has issued a strong buy rating on the company. The average 12 month price objective among brokers that have updated their coverage on the stock in the last year is $19.50.
LRMR has been the subject of several recent analyst reports. Baird R W raised shares of Larimar Therapeutics to a “strong-buy” rating in a report on Wednesday, September 4th. Robert W. Baird started coverage on shares of Larimar Therapeutics in a report on Wednesday, September 4th. They set an “outperform” rating and a $16.00 price target for the company. Wedbush assumed coverage on Larimar Therapeutics in a research report on Thursday. They set an “outperform” rating and a $22.00 price objective for the company. Finally, HC Wainwright began coverage on Larimar Therapeutics in a research note on Wednesday. They set a “buy” rating and a $15.00 target price for the company.
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Larimar Therapeutics Price Performance
Larimar Therapeutics stock opened at $6.52 on Friday. Larimar Therapeutics has a one year low of $2.18 and a one year high of $13.68. The company’s fifty day moving average price is $7.52 and its two-hundred day moving average price is $7.82. The company has a market capitalization of $415.99 million, a price-to-earnings ratio of -6.72 and a beta of 0.98.
Larimar Therapeutics (NASDAQ:LRMR – Get Free Report) last issued its quarterly earnings data on Wednesday, August 7th. The company reported ($0.34) earnings per share for the quarter, missing analysts’ consensus estimates of ($0.32) by ($0.02). As a group, sell-side analysts anticipate that Larimar Therapeutics will post -1.4 earnings per share 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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