Taysha gene therapies to participate in panel discussions at the lifesci partners 11th annual corporate access event

Dallas--(business wire)--taysha gene therapies, inc. (nasdaq: tsha), a patient-centric, pivotal-stage gene therapy company focused on developing and commercializing aav-based gene therapies for the treatment of monogenic diseases of the central nervous system (cns) in both rare and large patient populations, today announced that ra session ii, president, founder and ceo of taysha, will participate in two panel discussions during the lifesci partners 11th annual corporate access event. details for the panel discussions are below: title: gene therapy: reaching its full potential date: thursday, january 6, 2022 time: 11:00 am et webcast: https://wsw.com/webcast/lifesci3/panel8/2389200 title: patient advocacy: honing the skill for crossover communications between patients and stakeholders date: thursday, january 6, 2022 time: 2:00 pm et webcast: https://wsw.com/webcast/lifesci3/panel10/2456850 a webcast of the panels will be available in the “events & media” section of the taysha corporate website at https://ir.tayshagtx.com/news-events/events-presentations. archived versions of the webcasts will be available on the website for 60 days. about taysha gene therapies taysha gene therapies (nasdaq: tsha) is on a mission to eradicate monogenic cns disease. with a singular focus on developing curative medicines, we aim to rapidly translate our treatments from bench to bedside. we have combined our team’s proven experience in gene therapy drug development and commercialization with the world-class ut southwestern gene therapy program to build an extensive, aav gene therapy pipeline focused on both rare and large-market indications. together, we leverage our fully integrated platform—an engine for potential new cures—with a goal of dramatically improving patients’ lives. more information is available at www.tayshagtx.com.
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