Larimar Therapeutics, Inc. (NASDAQ:LRMR – Get Free Report) has been assigned a consensus rating of “Buy” from the nine research firms that are currently covering the company, MarketBeat Ratings reports. Eight investment analysts have rated the stock with a buy rating and one has assigned a strong buy rating to the company. The average twelve-month target price among brokers that have covered the stock in the last year is $19.67.
Several analysts have issued reports on the stock. HC Wainwright raised their price target on shares of Larimar Therapeutics from $15.00 to $16.00 and gave the stock a “buy” rating in a research report on Tuesday, March 25th. Citigroup restated a “buy” rating on shares of Larimar Therapeutics in a research report on Tuesday, March 25th. Guggenheim restated a “buy” rating and issued a $26.00 price target on shares of Larimar Therapeutics in a research report on Tuesday, March 25th. Finally, Robert W. Baird decreased their price target on shares of Larimar Therapeutics from $13.00 to $10.00 and set an “outperform” rating on the stock in a research report on Tuesday, March 25th.
Read Our Latest Stock Report on LRMR
Institutional Trading of Larimar Therapeutics
Larimar Therapeutics Trading Up 9.4%
NASDAQ:LRMR opened at $2.91 on Friday. Larimar Therapeutics has a 1 year low of $1.61 and a 1 year high of $11.20. The firm’s fifty day simple moving average is $2.15 and its 200 day simple moving average is $3.20. The firm has a market capitalization of $186.32 million, a PE ratio of -2.53 and a beta of 0.79.
Larimar Therapeutics (NASDAQ:LRMR – Get Free Report) last posted its quarterly earnings results on Wednesday, April 30th. The company reported ($0.46) earnings per share (EPS) for the quarter, missing the consensus estimate of ($0.42) by ($0.04). As a group, analysts anticipate that Larimar Therapeutics will post -1.15 EPS 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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