Positive results announced by the company Reata providing more support for the rationale to test their drug in neurodegenerative conditions such as Friedreich's ataxia.

Read press release here. This drug is the same as the one currently in trials around the world including at the London Ataxia Centre. See here for more information about taking part.

New method for diagnosing ARSACS discovered at Specialist Ataxia Centre in London

An Ataxia UK-funded research study on Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) has been published in the medical journal Brain. The study shows how a simple optical imaging technique can help provide an early diagnosis for ARSACS. Study lead Professor Paola Giunti (UCL Institute of Neurology, Head of the Ataxia Centre at UCL/UCLH and a BRC-funded Consultant) and colleague Dr Fion Bremner (also part of the Ataxia Centre), have used OCT to test a group of patients affected by ataxia to see if they could predict the genetic diagnosis causing ataxia in some patients. Read more about this study here.

Posted on 26/03/2018

New Options for Targeting Gene Mutation in Friedreich's Ataxia Described in Nucleic Acid Therapeutics

Researchers have shown that a wide variety of synthetic antisense oligonucleotides with different chemical modifications can activate the frataxin gene, which contains a mutation that decreases its expression in the inherited neurologic disorder Friedreich’s ataxia (FA). This new finding, which demonstrates a broad range of flexible options for identifying novel compounds capable of increasing frataxin protein expression and alleviating the effects of FA, is published in Nucleic Acid Therapeutics. You can find the article here.

Posted 22/03/2018

Working with Industry - message from patients

Last Autumn, Findacure organised a day workshop to focus on the partnerships between patients' groups and industry in the context of clinical research. Dr Julie Vallortigara, our research officer, attended this workshop and gave a talk about Ataxia UK's view and experience of working with pharmaceutical companies for ataxia research. David Bennett-Orphan diseases/UK specialist wrote an article about this very informative day. You can find this article on rarebase website here

Posted 23/02/2018