The Future of Advanced Therapeutics in Neurology

Connect with scientists rewriting the future for patients with the most complex diseases
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The Clinical Research Unit at The Neuro — one of the largest neurological trial centres in Canada — has been at the forefront of cutting-edge therapies for 40 years. Today, the Unit’s efforts to advance treatments are focussed on novel therapeutics which are poised to revolutionize neurological care.

This day-long event will bring together international leaders developing the latest generation of treatments. The symposium is designed for scientists, health professionals and stakeholders from academia and industry involved in the development of novel therapeutics for rare diseases and offers a unique opportunity to connect with international researchers.

The symposium is a satellite of the ASHG2026 annual meeting, and takes place the day before the start of their proceedings.

EVENT INFORMATION

Date: Monday, October 19, 2026
Sessions: 9am to 4:30pm
Networking cocktail: 4:30pm to 6pm

Location: Le Centre Sheraton
1201 boul. René-Lévesque Ouest
Montréal, Québec, H3B 2L7

Métro: Bonaventure

KEYNOTE SPEAKERS

Fyodor Urnov

Fyodor Urnov

We are excited to announce that two giants in the world of advanced therapeutics will be joining us as our keynote speakers. Fyodor Urnov is a professor of molecular therapeutics at the University of California, Berkeley and director for therapeutic R&D of its Innovative Genomics Institute (IGI).  

Prof. Urnov co-developed the toolbox of human genome and epigenome editing, co-named genome editing, and was on the team that advanced all of its first-in-human applications to the clinic. A key focus of his work has been expanding access to CRISPR therapies for genetic disease.  

A leader in his field, Phillip Zamore has been the Chair of the RNA Therapeutics Institute at UMass Chan Medical School for the past decade where his lab sought to understand the biology and mechanism of paradigmatic examples of Argonaute proteins and pathways, and, ultimately, to use these insights to design and improve small RNA-guided therapies for human diseases.

His research led to the development and FDA approval of small RNA drugs, including Onpattro, a first-of-its-kind RNAi therapeutic, for the treatment of the polyneuropathy of hereditary transthyretin-mediated (hATTR) amyloidosis in adults. 

 

Phillip Zamore

Phillip Zamore

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