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Financial Snapshot

Revenue
TTM
$0.00
Gross Margin
Last 4 Quarters
N/A
Net Income
TTM
-$87.50M
Current Assets
2026 Q1
Current Liabilities
2026 Q1
Current Ratio
2026 Q1
1415.62%
Total Assets
2026 Q1
Total Liabilities
2026 Q1
Book Value
2026 Q1
231.5M
Cash
2026 Q1
P/E
Last 4 Quarters
N/A
Free Cash Flow
TTM
-$98.42M

Stock Price

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Market Cap: $354.13 Million

About Lexeo Therapeutics Inc

Lexeo Therapeutics (NASDAQ: LXEO) is a clinical-stage gene therapy company focused on developing adeno-associated virus (AAV)-based treatments for genetic diseases, with a lead program targeting PKP2-arrhythmogenic cardiomyopathy (PKP2-ACM). The company generates no product revenue. Operations are funded entirely through equity issuances, including convertible preferred stock, common stock, pre-funded warrants, and warrants, as disclosed in the 10-K filed March 30, 2026. As of December 31, 2025, Lexeo held approximately $182.0 million in U.S. federal net operating loss carryforwards and $362.9 million in state and local NOLs, reflecting cumulative operating losses since inception. The lead candidate, LX2020, showed dose-dependent increases in PKP2 protein expression averaging 93% in low-dose and 162% in high-dose cohorts at three months across biopsied participants, based on data through January 2026. Net cash used in operating activities was $98.6 million in FY2025 versus $81.2 million in FY2024. CEO R. Nolan Townsend leads the company.

Revenue model
No product revenue as of the 10-K filed March 30, 2026. Operations funded through equity capital raises, including common stock and warrant issuances.
Products and services
LX2020: AAV-based gene therapy for PKP2-arrhythmogenic cardiomyopathy, in clinical-stage development as of January 2026 readout.
Customers and end markets
No commercial customers as of the 10-K filed March 30, 2026. End market is patients with genetic cardiac diseases, specifically PKP2-ACM. Counterparties include contract research organizations (CROs) and contract manufacturing organizations (CMOs) for preclinical and clinical development activities.
Value-chain role
Drug developer outsourcing preclinical studies to CROs and manufacturing to CMOs. No internal commercial manufacturing or sales infrastructure disclosed.
Geographic exposure
Operations based in the United States. Clinical and regulatory activities reference FDA jurisdiction primarily, with GDPR compliance noted for EEA and UK data handling.

Source: SEC 10-K, filed 2026-03-30

Industry: Biological Products, (No Diagnostic Substances) Peers: Annexon Inc Aura Biosciences Inc Avid Bioservices, Inc. Perspective Therapeutics Inc Janux Therapeutics Inc MeiraGTx Holdings PLC Nurix Therapeutics Inc Biohaven Ltd

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