Lexeo Therapeutics, Inc. (NASDAQ:LXEO – Get Free Report) has been given a consensus rating of “Buy” by the six ratings firms that are covering the stock, MarketBeat.com reports. Five investment analysts have rated the stock with a buy recommendation and one has assigned a strong buy recommendation to the company. The average twelve-month price objective among brokerages that have issued a report on the stock in the last year is $23.80.
Several brokerages recently weighed in on LXEO. HC Wainwright raised their target price on shares of Lexeo Therapeutics from $21.00 to $23.00 and gave the company a “buy” rating in a report on Thursday, November 14th. Royal Bank of Canada reissued an “outperform” rating and set a $24.00 price objective on shares of Lexeo Therapeutics in a report on Tuesday, January 21st. Chardan Capital raised their price objective on shares of Lexeo Therapeutics from $23.00 to $25.00 and gave the stock a “buy” rating in a report on Wednesday, November 13th. Finally, Leerink Partners cut their price objective on shares of Lexeo Therapeutics from $20.00 to $19.00 and set an “outperform” rating on the stock in a report on Wednesday, November 13th.
Check Out Our Latest Stock Analysis on LXEO
Hedge Funds Weigh In On Lexeo Therapeutics
Lexeo Therapeutics Trading Up 6.6 %
Shares of LXEO opened at $4.50 on Tuesday. The firm has a 50-day moving average price of $6.04 and a 200 day moving average price of $8.30. The firm has a market capitalization of $148.82 million, a P/E ratio of -1.42 and a beta of 2.99. Lexeo Therapeutics has a 12-month low of $3.84 and a 12-month high of $19.50. The company has a current ratio of 5.95, a quick ratio of 5.95 and a debt-to-equity ratio of 0.01.
About Lexeo Therapeutics
Lexeo Therapeutics, Inc operates as a clinical stage genetic medicine company that focuses on hereditary and acquired diseases. The company develops LX2006, which is an AAVrh10-based gene therapy candidate for the treatment of Friedreich's ataxia (FA) cardiomyopathy; LX2020, an AAVrh10-based gene therapy candidate for the treatment of plakophilin-2 arrhythmogenic cardiomyopathy; LX2021, a gene therapy candidate for the treatment of DSP cardiomyopathy associated with it; and LX2022, a gene therapy candidate for the treatment of hypertrophic cardiomyopathy, or HCM caused by TNNI3 gene.
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