Biopharma Transcript

Lexeo Therapeutics, Inc. LXEO

Nasdaq · Phase 2 · cardio-renal-metabolic · gene therapy · EDGAR · Updated Oct 24, 2026

Lexeo Therapeutics, Inc. (Nasdaq: LXEO) is a cardio-renal-metabolic drug developer. Its lead program, LX2006 (AAVrh10 frataxin gene therapy), is in Phase 2 for Friedreich ataxia cardiomyopathy. Its next catalyst on record is Mantle / acquired FA programs: Program prioritization update for acquired FA programs expected in early 2027. (2027).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: Mantle / acquired FA programs — Program prioritization update for acquired FA programs expected in early 2027. (2027). 3 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
LX2006 (SUNRISE-FA Phase 1/2; SUNRISE-FA 2 pivotal study; Cornell investigator-initiated trial)Friedreich ataxia cardiomyopathygene therapyPhase 2
LX2020 (AAVrh10 PKP2 gene therapy), HEROIC-PKP2 Phase 1/2PKP2 arrhythmogenic cardiomyopathygene therapyPhase 1
LX2021 (connexin 43 gene therapy)Desmoplakin cardiomyopathy / dilated cardiomyopathygene therapyPre-clinical

Recent results and decisions

  1. Sep 22, 2026
    n/a Lexeo to acquire Mantle Therapeutics (one clinical-stage oral program, two preclinical, one discovery) for $8.3M upfront plus up to $13M milestones, and signed three CNS-targeted gene therapy research collaborations for FA.Mantle acquisition and three new research collaborations Filing
  2. Sep 22, 2026
    positive Acquired oral program LX3010: approximately six-point mFARS improvement at 16 weeks and mean nine-fold frataxin increase in muscle biopsies across 11 FA patients.Approximately six-point improvement in mFARS scores at 16 weeks Mean nine-fold increase in frataxin protein levels from baseline in muscle biopsies across 11 FA patients Filing
  3. Aug 12, 2026
    started SUNRISE-FA 2 pivotal study initiated in June 2026 with first site activated and first patient enrolled.The study was initiated in June with activation of the first trial site and enrollment of the first patient. Filing

8 more on record.

For subscribers

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