Lexeo Therapeutics (NASDAQ: LXEO) recently received a number of ratings updates from brokerages and research firms:
- 4/8/2025 – Lexeo Therapeutics had its price target lowered by analysts at Chardan Capital from $25.00 to $22.00. They now have a “buy” rating on the stock.
- 4/8/2025 – Lexeo Therapeutics had its “buy” rating reaffirmed by analysts at HC Wainwright. They now have a $23.00 price target on the stock.
- 3/26/2025 – Lexeo Therapeutics had its “buy” rating reaffirmed by analysts at HC Wainwright. They now have a $23.00 price target on the stock.
- 3/25/2025 – Lexeo Therapeutics had its price target lowered by analysts at Royal Bank of Canada from $24.00 to $20.00. They now have an “outperform” rating on the stock.
- 3/25/2025 – Lexeo Therapeutics had its “buy” rating reaffirmed by analysts at Chardan Capital. They now have a $25.00 price target on the stock.
- 3/24/2025 – Lexeo Therapeutics had its price target lowered by analysts at Leerink Partners from $19.00 to $18.00. They now have an “outperform” rating on the stock.
Lexeo Therapeutics Trading Down 8.1 %
LXEO opened at $2.17 on Friday. The company has a debt-to-equity ratio of 0.01, a quick ratio of 5.95 and a current ratio of 5.95. Lexeo Therapeutics, Inc. has a one year low of $1.45 and a one year high of $19.50. The company has a market cap of $72.04 million, a P/E ratio of -0.69 and a beta of 1.52. The business’s 50-day simple moving average is $3.40 and its 200-day simple moving average is $6.02.
Lexeo Therapeutics (NASDAQ:LXEO – Get Free Report) last announced its quarterly earnings results on Monday, March 24th. The company reported ($0.78) earnings per share (EPS) for the quarter, beating analysts’ consensus estimates of ($0.87) by $0.09. As a group, equities research analysts expect that Lexeo Therapeutics, Inc. will post -3.14 EPS for the current fiscal year.
Institutional Investors Weigh In On 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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