AlterRNA Therapeutics is a patient-driven biotech company founded by a father after his child was diagnosed with MPAN. We are building collaborative, affordable research and treatment development pathways for rare genetic disorders.
AlterRNA is dedicated to developing next-generation RNA therapeutics that address the underlying genetic causes of disease. AlterRNA was founded to help close the gap between genetic diagnosis and therapeutic development for rare diseases by connecting patient need, RNA science, clinical insight, and collaborative development.
Precisely targeting specific genetic mutations
Pioneering novel RNA modification technologies
Driven by the needs of patients and their families
Committed to rigorous research and development

Our pipeline targets rare genetic diseases across multiple therapeutic areas, bringing hope to patients with limited treatment options.
AlterRNA is dedicated to developing next-generation RNA therapeutics
This research is for Human BBB platform for organ specific…
Novel approach to treating lysosomal storage diseases through targeted mRNA…
Join our secure network of researchers, clinicians, and partners to share insights, discuss methodologies, and advance the field of RNA therapeutics together.
AlterRNA offers unique opportunities for investors to fund high-potential therapeutic projects with full transparency and data-backed milestones.
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