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Gene therapy platform for lysosomal storage diseases

01 / 03

A new gene therapy platform for lysosomal storage diseases enables parallel development, reducing time, costs and improving sustainability for rare disease treatments.

Announced FDA approval of Waskyra™

02 / 03

Fondazione Telethon announces that the U.S. Food and Drug Administration (FDA) has approved the Biologics License Application (BLA) for Waskyra, an ex vivo gene therapy for patients with Wiskott-Aldrich syndrome (WAS).

Our commitment on therapies for rare genetic diseases

03 / 03

Our research has pinpointed promising therapeutic strategies for combating a number of diseases. Read more about therapies already authorized and those currently in development.

Our numbers

Since 1990 we fund research on rare genetic conditions
  • 741 Millions of euros invested
  • 1.916 Researchers
  • 3.118 Projects funded

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