Full Press Release Details
DALLAS, May 10, 2022 (GLOBE NEWSWIRE) -- 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 oral and poster presentations and a company-sponsored symposium at the upcoming 25th Annual Meeting of the American Society of Gene & Cell Therapy (ASGCT) taking place in Washington, D.C. from May 16-19, 2022.
3: Vagus Nerve Delivery of AAV9 to Treat Autonomic Nervous System Dysfunction in Giant Axonal Neuropathy
Presenter – Rachel Bailey, UT Southwestern
Date/Time – Monday, May 16th at 10:45 AM Eastern Time
470: Vectorized Delivery of Tau Reduction Therapy as a Treatment Approach for Tauopathies
Presenter – Rachel Bailey, UT Southwestern
Date/Time – Tuesday, May 17th at 4:15 PM Eastern Time
Poster Presentations
157: Preclinical Gene Therapy with AAV9/SLC6A1 in a Mouse Model of SLC6A1 Related Disorder
Presenter – Weirui Guo, UT Southwestern
Date/Time – Monday, May 16th at 5:30 PM Eastern Time
Location – Poster Board M-38, Hall D
179: shRNA-Mediated Gene Therapy for the Treatment of Prader-Willi Syndrome
Presenter – Violeta Zaric, UT Southwestern
Date/Time – Monday, May 16th at 5:30 PM Eastern Time
Location – Poster Board M-60, Hall D
640: Gene Therapy Treatment in Young SLC13A5 Deficient Mice
Presenter – Rachel Bailey, UT Southwestern
Date/Time – Tuesday, May 17th at 5:30 PM Eastern Time
Location – Poster Board Tu-145, Hall D
557: shRNA-Mediated Gene Therapy for the Treatment of Angelman Syndrome
Presenter – Hye Ri Kang, UT Southwestern
Date/Time – Tuesday, May 17th at 5:30 PM Eastern Time
Location – Poster Board Tu-62, Hall D
642: Safety and Biodistribution Assessment in Non-Human Primates (NHPs) of a miniMECP2 AAV9 Vector for Gene-Replacement Therapy of Rett Syndrome
Presenter – Dr. Suyash Prasad, Taysha Gene Therapies
Date/Time – Tuesday, May 17th at 5:30 PM Eastern Time
Location – Poster board Tu-147, Hall D
1037: Safety Assessment of High-Dose miniMECP2 AAV9 Gene-Replacement Therapy (TSHA-102) for Rett Syndrome in Rats
Presenter – Mary Newman, Taysha Gene Therapies
Date/Time – Wednesday, May 18th at 5:30 PM Eastern Time
Location –Poster board W-163, Hall D
Taysha-Sponsored Symposium
Accepting the Challenge: Innovative Approaches and Translational Strategies in Gene Therapy Development
Presenters – Dr. Suyash Prasad, Taysha Gene Therapies, Dr. Steven Gray, UT Southwestern, and Dr. Kimberly Goodspeed, UT Southwestern
Date/Time – Tuesday, May 17th at 12:00 PM Eastern Time
Additional details can be found at the ASGCT 25th Annual Meeting website.
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.
Chief Corporate Affairs Officer
Taysha Gene Therapies
Canale Communications