Lexeo Raises $100m To Advance CNS Candidates, Validate Cardiac Gene Therapies

Start-Up Has Brought In $185m In Less Than A Year

The company, which has treatments in the clinic for CLN2 Batten disease and APOE4-associated Alzheimer’s disease, is developing AAV-mediated gene therapies designed for safer outcomes.

Gene therapy concept vector illustration
Lexeo will take its first gene therapy for a rare cardiomyopathy into the clinic within the next few months • Source: Alamy

Lexeo Therapeutics has accomplished a lot in the nine months since it launched with $85m in series A venture capital for development of AAV-mediated gene therapies that treat rare and prevalent monogenic central nervous system and cardiac diseases. And now, after acquiring four cardiomyopathy programs, the company has closed a $100m series B round to fund its two clinical-stage treatments for CNS diseases, pursue clinical validation for gene therapies in rare cardiac indications and advance its preclinical programs.

CEO R. Nolan Townsend told Scrip that he is encouraged by recent discussions about the safety of AAV-based gene therapies,...

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