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SIRION Biotech and Denali Therapeutics Join Forces to Develop Gene Therapies for Diseases of the Central Nervous SystemMunich, Germany, )
AAV vectors are considered the most promising gene delivery system for therapeutic applications. Denali Therapeutics, together with SIRION Biotech and Dirk Grimm, a world-renowned and pioneering scientist in the field of AAV biology and application, will combine their proprietary technology platforms to create a next generation of AAV vectors. The goal is to develop new and modified AAV capsids exhibiting a safe product profile with improved specificity and high efficiency for therapeutic drug delivery to the brain at therapeutic levels to effectively treat patients. “This ground-breaking collaboration will help Denali Therapeutics to increase the availability of protein therapeutics in the brain, and to quickly enter clinical trials with efficient, safe and scalable therapeutic candidates”, said Dr. Christian Thirion, founder and CEO of the company. “We believe that through our partnership with Denali, CNS-directed AAV-based gene therapies can reach the market i n the fastest possible way, providing novel treatment options to many millions of patients worldwide suffering from devastating neurodegenerative diseases such as Parkinson’s, Alzheimer’s, and ALS,” added Dr. Sabine Ott, VP BD & Licensing. Prof. Dirk Grimm notes that "By contributing and harnessing our unique and proprietary expertise in the engineering and high-throughput in vivo screening of AAV capsid libraries, we will significantly accelerate this joint endeavour and increase our chances to realize its pivotal aims."
Additionally, Alexander Schuth, COO of Denali Therapeutics stated, “We are excited to partner with SIRION Biotech and combine our expertise around the blood-brain barrier and neurodegenerative diseases with SIRION’s leading expertise on viral vectors for gene therapy to enable new treatments for diseases of the brain. This partnership will add a new therapeutic modality to our portfolio and is complementary to our existing biotherapeutic and small molecule programs.”
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