At HaliGene, we operate with a lean, collaborative structure designed for capital efficiency and translational impact. Our team works closely with academic researchers, clinicians, and patient groups to accelerate discovery and development while maintaining a science-first approach. Together, we are building a sustainable gene therapy engine capable of delivering innovative treatments, including our lead program, HG-001, a gene replacement therapy for congenital megaconial muscular dystrophy (MDCMC).
Through partnership, scientific leadership, and community engagement, we aim to fundamentally change what is possible for families living with ultra-rare neuromuscular and metabolic conditions.
With a small, dedicated team and a platform built for efficiency, HaliGene pledges to bring forward gene therapy candidates that reflect the highest standards of scientific excellence while honouring the urgent needs of the patients and families we serve.





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