Lexeo Therapeutics, Inc./$LXEO

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About Lexeo Therapeutics, Inc.

Lexeo Therapeutics Inc is a clinical-stage genetic medicine company engaged in the development of gene therapy candidates targeting the underlying genetic causes of cardiovascular diseases. The company is advancing a portfolio of programs focused on conditions such as Friedreich ataxia, cardiomyopathy, plakophilin-2, or PKP2, and arrhythmogenic cardiomyopathy, with its lead candidates including LX2006 and LX2020. Its therapies utilize AAV-based vectors designed to deliver functional genes to cardiac cells to restore normal function and address high unmet medical needs.
Ticker
$LXEO
Sector
Health
Primary listing
NASDAQ
Employees
63

LXEO Metrics

BasicAdvanced
$349M
-
-$1.15
1.47
-

Bulls say / Bears say

Lexeo finalized its SUNRISE-FA 2 pivotal trial protocol and statistical analysis plan for LX2006, aligning with FDA feedback to initiate enrollment by end-June 2026 and targeting topline data in H2 2027, thereby de-risking its regulatory pathway. (Reuters)
A corporate deck released in March 2026 highlighted interim Phase I/II efficacy and safety results for LX2006, reporting mean LVMI reductions of 18% at six months and 23% at 12 months with no Grade 3 treatment-related serious adverse events, exceeding FDA-aligned targets. (Reuters)
Lexeo is showcasing its pipeline breadth and manufacturing readiness with presentations at the ASGCT Annual Meeting in May 2026, covering updated LX2006 data, preclinical TNNI3 cardiomyopathy work, and AAV manufacturing comparability, underscoring advancing technical progress. (Reuters)
Lexeo's FY25 net loss widened to USD 100 million despite a year-end cash position of USD 250 million, indicating a high cash burn rate that may require additional capital before commercialization. (Reuters)
Even after finalizing its pivotal trial design, Lexeo’s shares remain down approximately 50% year-to-date, reflecting persistent investor skepticism about its near-term value drivers. (Reuters)
The SUNRISE-FA 2 trial’s open-label design without a placebo or sham procedure, as advised by the FDA, could introduce bias and limit the interpretability of efficacy results, potentially complicating regulatory review. (Reuters)
Data summarised monthly by Lightyear AI. Last updated on 24 Aug 2026.

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