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16.12.25

From Wiskott–Aldrich Syndrome to a new model for gene therapies

Rare and ultra-rare genetic diseases pose profound scientific, human and economic challenges. The development of gene therapy for Wiskott–Aldrich syndrome (WAS) is a clear example of this complexity.

From Research

15.12.25

Fondazione Telethon and Orphan Therapeutics Accelerator Sign Memorandum of Understanding to Pioneer Non-Profit Commercial Access Model for Ultra-Rare Disease Gene Therapy in the US

Orphan Therapeutics Accelerator and Fondazione Telethon today announced the signing of a Memorandum of Understanding to facilitate US commercial access to an ex vivo gene therapy for the treatment of Wiskott-Aldrich syndrome.

From Telethon Foundation

10.12.25

Fondazione Telethon Announces FDA approval of Waskyra™ (etuvetidigene autotemcel), a Gene Therapy for the Treatment of Wiskott-Aldrich Syndrome

The therapy represents a major scientific and clinical achievement, offering new hope for patients affected by this condition.

From Telethon Foundation

05.12.25

Engineering peripheral immune tolerance: Tregs and beyond

Tregs and beyond: discover how SR-TIGET scientists are engineering peripheral immune tolerance for tomorrow’s precision therapies.

From Research

14.11.25

CHMP positive opinion for Waskyra™, a gene therapy for the treatment of Wiskott-Aldrich syndrome (WAS)

Announced the positive opinion issued by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA), recommending marketing authorisation in the European Union for Waskyra™, an ex vivo gene therapy for Wiskott-Aldrich Syndrome.

From Telethon Foundation

13.11.25

Cracking the Code: IPEX, FOXP3 and the Path to Gene Therapy

Discover how SR-TIGET scientists advanced the genetics of peripheral immune tolerance, from FOXP3 and IPEX to gene therapy using lentiviral vectors.

From Research

04.11.25

The origins of peripheral immune tolerance: SR-TIGET's contribution to a Nobel-winning field

Discover how SR-TIGET scientists helped shape the science of peripheral immune tolerance, from the discovery of Treg and Tr1 cells to early gene therapy.

From Research

16.10.25

Attya Omer Named Runner-Up in the Nature Inspiring Women in Science Awards

The scientist of SR-TIGET and Università Vita-Salute San Raffaele recognized internationally for her vision in advancing gene therapy and inspiring women in science.

From Research

23.09.25

The Armenise-Harvard Foundation invests one million dollars in brain research

Thanks to the Career Development Award, neuroscientist Gabriele Ciceri will establish a new laboratory at the San Raffaele-Telethon Institute for Gene Therapy.

From Research

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