A first group of patients has been treated with LX2006, an investigational gene therapy for heart disease in people with Friedreich’s ataxia (FA), in a Phase 1/2 clinical trial and dosing has begun in a second group. According to Lexeo Therapeutics, the treatment’s developer, LX2006 has been well tolerated and not associated with unexpected safety concerns or toxicity. “New treatment approaches, like LEXEO’s LX2006 gene therapy candidate, are critical for individuals and caregivers confronted with the debilitating realities of FA,” says Jennifer Farmer, CEO of the Friedreich’s Ataxia Research Alliance. Click here to learn more. |