Vincenzo Silani

Vincenzo Silani

Professor of Neurology and Chairman

Vincenzo Silani is Professor of Neurology, Director of the Department of Neurology-Stroke Unit and Laboratory of Neuroscience of the University of Milan Medical School at the IRCCS Istituto Auxologico Italiano in Milano. He is also the Scientific Director of the “Dino Ferrari” Center for Neuromuscular and Neurodegenerative Disease. In 1979-81 he was a post-doctoral fellow in the Department of Neurology-Baylor College of Medicine in Houston and a Visiting Professor in Neurology in 1999. He was co-chairman (2002-2005) and chairman (2005-2007) of the European ALS Consortium (EALSC); co-director of the European Academy of Neurology Subspeciality Panel ALS and Frontotemporal Dementia (2003-2019).  He is author of more than 300 scientific publications in major international journals. He is internationally recognised as a leading scientist in ALS/FTD and he established an ALS/FTD/PD Centre in Milan with a large database of familiar and sporadic cases. He founded the SLAGEN Consortium in Italy (2010). He largely contributed in defining the expression of different new genes in both SALS and FALS, investigating the functional role of TDP43, FUS/TLS, and C9ORF72 using iSCPs. He has been P.I. of many clinical trials and recipient of several grants.

Connect
Connect trials
Active
Phase ii

RT001 in Amyotrophic Lateral Sclerosis

Industry trial

In this phase 2 trial, we will study the safety and efficacy of the compound RT001 in people living with ALS. This clinical trial is sponsored by Retrotope Inc.

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Active
Phase iii

ALXN1210-ALS-308 trial

Industry trial

This phase 3 trial aims to study the safety and efficacy of the drug ‘ravulizumab’ in people living with ALS. To register for this study, you should contact your local ALS centre or treating physician.

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Active
Phase iii

VALOR study

Industry trial

Biogen is conducting a clinical trial to evaluate the safety and potential efficacy of an investigational drug for people with Amyotrophic Lateral Sclerosis (ALS) with a SOD1 gene mutation.

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Recruiting
Phase iii

TUDCA-ALS

Investigator initiated trial

This trial will evaluate the efficacy of tauroursodeoxycholic acid (TUDCA) as add-on treatment for people with ALS.

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