Fortress Biotech forms new subsidiary, Aevitas Therapeutics
Subsidiary to develop novel AAV gene therapy treatments for complement-mediated.
Fortress Biotech has formed a new subsidiary company, Aevitas Therapeutics, to develop novel gene therapy approaches for complement-mediated diseases. The proprietary technology, licensed from a leading university, uses adeno-associated virus (AAV)-based gene therapy to restore lasting production of functional complement regulatory proteins, providing a potentially curative treatment.
Irregularities in these proteins can play a vital role in an array of complement-mediated diseases, including atypical hemolytic uremic syndrome (aHUS) and paroxysmal nocturnal hemoglobinuria (PNH). Recent research has suggested that complement regulatory proteins could also play a key role in the pathogenesis of age-related macular degeneration.
Dr Lindsay A. Rosenwald, Fortress Biotech’s Chairman, President and Chief Executive Officer, said: “We are thrilled to work on this potentially groundbreaking technology in numerous areas of unmet need as we continue to establish our capabilities in the gene therapy space.”
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