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LXEO US Equity

Lexeo Therapeutics, Inc.Health Care · Biological Products, (No Diagnostic Substances) · CIK 1907108 · FY ends Dec 31
$4.93
-0.05 (-1.00%)
USD · as of 2026-08-18 · marketstack
8 registered studies · 7 active

Studies where LXEO is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

5 interventional · 3 observational

Held by 8 tracked-famous managers (CITADEL ADVISORS LLC, MILLENNIUM MANAGEMENT LLC, Balyasny Asset Management L.P., Qube Research & Technologies Ltd, Squarepoint Ops LLC, +3 more) · FINRA short interest 16.9 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Study of LX2006 Gene Therapy in Friedreich Ataxia CardiomyopathyNCT07721025Percent change from baseline in left ventricular mass index by cardiac MRIRandomized · Single-masked · TreatmentPhase 2RecruitingGenetic: LX2006 · Other: Usual CareFriedreich Ataxia, Cardiomyopathy, Secondary26Jun 2032≤ 2,142 d2026-07-22
Long-term Follow-up Study of Gene Therapy for Arrhythmogenic Cardiomyopathy Due to a Plakophilin-2 Pathogenic VariantNCT07050160observationalPercentage of subjects who experienced at least 1 treatment emergent adverse event (TEAE) and/or 1 treatment emergent serious adverse event (TESAE).Enrolling by invitationArrhythmogenic Cardiomyopathy, PKP2-ACM, PKP2-ARVC10Aug 2030≤ 1,473 d2025-11-12
Gene Therapy for Cardiomyopathy Associated With Friedreich's AtaxiaNCT05445323Treatment-emergent adverse events (TEAEs) and Treatment-emergent serious events (TESAEs)Open-label · TreatmentPhase 1/2Active, not recruitingGenetic: Low dose LX2006, Mid Dose LX2006, High Dose LX2006Friedreich Ataxia, Cardiomyopathy, Secondary8Sep 2029≤ 1,138 d2025-12-23
Long-Term Follow-up of Gene Therapy for APOE4 Homozygote Alzheimer's DiseaseNCT05400330Incidence of treatment emergent adverse eventsOpen-label · TreatmentPhase 1Active, not recruitingBiological: LX1001Alzheimer Disease10Nov 2028≤ 834 d2025-07-01
Clinical Course Of Disease In Participants With FA-CMNCT06865482observationalCharacterize cardiac disease presentation and progression among participantsRecruitingFriedreich Ataxia, Cardiomyopathy65Sep 2027≤ 407 d2026-06-08
A Study to Assess Real-world Patient Characteristics and Clinical Course for Symptomatic Patients With PKP2-ACMNCT06976606observationalPremature ventricular contractions (PVC)RecruitingArrhythmogenic Cardiomyopathy, PKP2-ACM, PKP2-ARVC40Jul 2027≤ 346 d2025-05-16
Gene Therapy for ACM Due to a PKP2 Pathogenic VariantNCT06109181Percentage of subjects who experienced at least 1 treatment emergent adverse event (TEAE) and/or 1 treatment emergent serious adverse event (TESAE).Open-label · TreatmentPhase 1/2Active, not recruitingGenetic: LX2020Arrhythmogenic Cardiomyopathy, PKP2-ACM, PKP2-ARVC10Dec 2026≤ 134 d2025-11-12
Gene Therapy for APOE4 Homozygote of Alzheimer's DiseaseNCT03634007Proportion of participants with treatment-emergent adverse events and serious adverse eventsNon-randomized · Open-label · TreatmentPhase 1/2CompletedBiological: LX1001Alzheimer Disease, Early Onset Alzheimer Disease152024-11-07actual2025-10-20

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19