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LEXEO THERAPEUTICS

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$8.725 0.0409(4.09%) LXEO at 04 Dec 2025 04:38 PM Biotechnology
Lowest Today 8.32
Highest Today 8.72
Today’s Open 8.37
Prev. Close 8.32
52 Week High 10.38
52 Week Low 1.45
Day’s Range: Low 8.32 High 8.72
52-Week Range: Low 1.45 High 10.38
1 day return -
1 Week return -12.22
1 month return +3.65
3 month return +73.96
6 month return +178.29
1 year return +28.22
3 year return -
5 year return -
10 year return -

Institutional Holdings

Market Status

Strong Buy: 4

Buy: 3

Hold: 0

Sell: 0

Strong Sell: 0

Fundamentals

Market Cap 607.25 M

PB Ratio 5.9559

PE Ratio 0.0

Enterprise Value 605.35 M

Total Assets 146.94 M

Volume 1357693

Company Financials

Annual Revenue FY23:0 0.0M, FY22:654000 0.7M, FY21:1657000 1.7M, FY20:518476 0.5M

Annual Profit FY23:null 0.0M, FY22:654000 0.7M, FY21:1657000 1.7M, FY20:518476 0.5M

Annual Net worth FY23:-66784000 -66.8M, FY22:-59277000 -59.3M, FY21:-50622000 -50.6M, FY20:-5152788 -5.2M

Quarterly Revenue Q3/2025:0 0.0M, Q2/2025:0 0.0M, Q1/2025:0 0.0M, Q3/2024:0 0.0M, Q2/2024:0 0.0M

Quarterly Profit Q3/2025:-530000 -0.5M, Q2/2025:-510000 -0.5M, Q1/2025:-501000 -0.5M, Q3/2024:null 0.0M, Q2/2024:-496000 -0.5M

Quarterly Net worth Q3/2025:-20283000 -20.3M, Q2/2025:-26103000 -26.1M, Q1/2025:-32656000 -32.7M, Q3/2024:-29489000 -29.5M, Q2/2024:-21238000 -21.2M

Fund house & investment objective

Company Information Lexeo Therapeutics, Inc., a clinical stage genetic medicine company, focuses on hereditary and acquired diseases with high unmet need in the United States. Its product pipeline comprises LX2006, an AAVrh10-based gene therapy candidate, which is in phase 1/2 clinical trial to treat friedreich ataxia cardiomyopathy; LX2020, an AAVrh10-based gene therapy candidate, which is in phase 1/2 to deliver a functional plakophilin-2 (PKP2) gene to cardiac muscle for the treatment of PKP2-ACM; and LX2021, a gene therapy candidate, which is in preclinical trial to deliver the coding sequence for the functional connexin 43, or Cx43, protein for a group of inherited cardiac muscle disorders associated with a high risk of sudden death, including arrhythmogenic cardiomyopathy (ACM) and certain forms of dilated cardiomyopathy. The company also develops LX2022, a gene therapy candidate, which is in preclinical trial to deliver a functional TNNI3 gene to myocardial cells to treat a distinct form of hypertrophic cardiomyopathy. In addition, it is developing LX1001, an AAVrh10-based gene therapy candidate, which has completed phase 1/2 clinical trial for the treatment of APOE4-associated Alzheimer's disease. The company has license agreement with Cornell University to conduct of the Phase 1/2 clinical trial of LX1001, as well as support the development of LX1004 program; research collaboration agreement with Cornell University to conduct preclinical research to develop the licensed technology; and third license agreement which obtained certain rights for FA cardiomyopathy, including rights to current and future clinical data from an ongoing Cornell University investigator-initiated Phase 1A trial of a gene therapy candidate. The company was founded in 2017 and is headquartered in New York, New York.

Organisation Biotechnology

Employees 61

Industry Biotechnology

CEO Mr. R. Nolan Townsend

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