05.04.22

Gene therapy targeted to the brain: a complex but not impossible challenge

Angela Gritti from the San Raffaele Telethon Institute of Milan talks about the efforts of applying gene therapy to one of the most difficult body organs to access.

From Research

09.03.22

Aicardi-Goutières syndrome: when the immune system detects viruses where there are none

An interview with Anna Kajaste-Rudnitski from the San Raffaele Telethon Institute for Gene Therapy in Milan, author of a study that gives new insights into this rare syndrome and provides also useful information to investigate the interaction between the immune system and viruses, including Sars-CoV-2.

From Research

21.12.20

Orchard Therapeutics Receives EC Approval for the Treatment of Early-Onset MLD

First gene therapy to receive full EU marketing authorization for eligible MLD patients.

From Telethon Foundation

03.11.20

Potential adverse reaction to gene therapy in a patient treated with Strimvelis for the treatment of ADA-SCID

Fondazione Telethon has recently learned that a patient suffering from a rare immunodeficiency of genetic origin, ADA-SCID, and treated in 2016 with gene therapy has developed leukemia.

From Telethon Foundation

16.10.20

Orchard Therapeutics Receives Positive CHMP Opinion for the Treatment of Early-Onset MLD

First therapy recommended for EU approval for eligible patients with confirmed diagnosis of late infantile or early juvenile MLD variants.

From Research

07.09.20

Osteopetrosis: new opportunity of treatment thanks to a licensing agreement

SiSaf announces a research collaboration and licensing agreement with the University of L’Aquila for the treatment of the debilitating bone disease, Autosomal Dominant Osteopetrosis Type 2.

From Research

10.07.20

Discovery of a novel drug candidate to develop effective treatments for brain disorders

Researchers at IIT-Istituto Italiano di Tecnologia discovered a novel chemical compound, which has the potential to became a new drug for the treatment of core symptoms of brain disorders like Down syndrome and autism.

From Research

01.07.20

Study of genetic condition leads to discovery of mechanism that promotes cance development

At TIGEM scientist have described how the study of a rare genetic condition has provided the key to understanding a mechanism that leads to the formation of cysts and tumours in certain organs, in particular the kidneys.

From Research

04.06.20

Groundbreaking Gene Therapies for Hereditary Diseases

Alessandro Aiuti, a physician and research scientist from Milan, receives the Else Kröner Fresenius Prize for Medical Research 2020 endowed with 2.5 million euros.

From Telethon Foundation

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