Adrestia Therapeutics Partners with Leading Patient Advocacy Groups to Form Ataxia Telangiectasia Research Consortium
Adrestia Therapeutics, a leader in synthetic rescue therapies for genetic diseases, today announced it has co-founded a research consortium to find new treatments for ataxia telangiectasia (AT), a fatal, inherited, progressive neurodegenerative disorder that is typically diagnosed in young children. The consortium’s other founding members include the A-T Children’s Project, the AT Society and Action for AT. Adrestia is applying its synthetic rescue technology to systematically mine the human genome for novel targets which could be used as the basis for therapies for AT and related diseases. Currently, there are no corrective therapies for AT.
“The entire Adrestia team is moved by the dedication of the AT community and we are honored to be working closely with our consortium partners to combine patient networks, scientific and other resources to accelerate the development of new treatment options, for which there is a desperate need,” said Robert Johnson, Chief Executive Officer of Adrestia. “Many genetic diseases are untreatable with current technologies. The power of our synthetic rescue approach lies in its ability to reveal alternative therapeutic targets which lie outside the core biological pathway. Our ultimate goal is to develop effective medicines which rebalance the underlying biology, unlocking new ways of treating intractable genetic diseases. AT and several related conditions are caused by an inability to repair DNA damage normally. We believe the same synthetic rescue targets may be useful for a range of common diseases which also involve DNA damage repair defects.”
“AT has a devastating impact on families around the world and despite its severity and the clear understanding of its primary cause, we still cannot change the course of the disease. We welcome innovative approaches that can move us towards treatments or cures,” said Professor Penny Jeggo, noted DNA damage researcher and Trustee of the AT Society. Brad Margus, founder and Board chair of the A-T Children’s Project, added, “We are proud to begin this new initiative with Adrestia as we drive towards a brighter future for our community.”
“As a group deeply involved with advancing therapeutic research, we know collaboration and medical innovation are the path to a future where the effects of AT are minimised,” said Sean Kelly, Chief Executive of Action for AT. “We are proud to join this consortium and support a new line of promising research alongside other tireless advocacy groups.”
A wealth of human genetic data has revealed that a range of common chronic diseases are driven by defects in DNA damage repair, which are also the root cause of ataxia telangiectasia and other related inherited conditions. These common diseases span neurodegeneration, immune dysfunctions, cardiovascular disease, diabetes and metabolic diseases. Adrestia’s co-founding scientist, Professor Steve Jackson, is a noted expert in DNA damage repair biology whose work led to olaparib. Olaparib was the first approved cancer drug to exploit DNA damage repair mechanisms via a mechanism termed synthetic lethality, paving the way to applying complementary principles to discover new drugs for genetic diseases.
About ataxia telangiectasia
Ataxia telangiectasia (AT) is an inherited, fatal disorder primarily driven by mutations in the ATM gene, which is involved in DNA damage repair. Symptoms vary between individuals but typically involve degeneration across a range of neurological and neuromuscular functions, impaired metabolic and immune system function, among others. People with AT often require significant support and face a significantly reduced life expectancy. Historical estimates of how many people are affected by the disease vary, but recent data suggests the prevalence may be significantly underestimated, with at least 3,000 diagnosed patients in the USA.
About the AT Society
The AT Society exists to enable people with AT to make the most of the lives they have. They provide specialist emotional and practical support for children and their families affected by AT, and fund medical research to improve treatments and ultimately find a cure. The AT Society is based in the United Kingdom and more information can be found at www.atsociety.org.uk. The AT Society is currently the subject of a BBC Lifeline appeal running in February 2023, with more information and opportunities to donate available at https://www.bbc.co.uk/programmes/m001hr2b.
About the A-T Children’s Project
The nonprofit A-T Children's Project partners with academic and industry investigators worldwide - organizing and supporting innovative research, conferences, clinical teams, data platforms, and biomarkers - to optimize disease management strategies, develop new treatments and find a cure for ataxia-telangiectasia. For more information see http://www.atcp.org.
About Action for A-T
Action for A-T funds medical research to speed up the process of identifying a cure for Ataxia Telangiectasia or treatments that delay or prevent the disabling effects of this devastating childhood condition. Action for A-T provides a dedicated funding stream for medical research. Its sole focus is to raise funds for this purpose; as well as working to drive research and awareness of A-T. Over the last few years, Action for A-T has become the leading charitable funders of A-T medical research in the UK. For more information see http://www.actionforat.org.
About Adrestia
Adrestia is a leader in synthetic rescue therapies for genetically defined diseases. As many directly causative gene mutations are not druggable, synthetic rescue identifies drug targets in a much wider network of functionally connected genes. The aim is to correct the effects of the causative mutations and ‘rescue’ health. Adrestia is creating a synthetic rescue ‘Atlas’ of the human genome and advancing a portfolio of first-in-class oligonucleotide or oral small molecule therapies, initially for neurologic, neuromuscular and cardiomyopathic diseases. Adrestia’s platform and in-house programs are complemented by a target discovery alliance with GSK and a Huntington’s disease collaboration with noted researchers including Dr Sarah Tabrizi at University College London.
Adrestia was co-founded by Professor Steve Jackson and the deep technology investment fund Ahren Innovation Capital, which co-led Adrestia’s Series A financing along with GSK. Jackson co-originated the first synthetic lethality drug, olaparib, which was the first drug approved to treat cancers caused by inherited mutations. For further information, visit: www.adrestia.com.
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