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Taysha Gene Therapies Announces Oral Presentations at the Upcoming 2022 IRSF Rett Syndrome Scientific Symposium and the ASCEND National Summit

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DALLAS, April 25, 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 presentations at the upcoming International Rett Syndrome Foundation (IRSF) Rett Syndrome Scientific Symposium taking place in Nashville, Tennessee April 26 – 27, 2022, and the ASCEND Rett Syndrome National Summit taking place in Nashville, Tennessee April 27 – 30, 2022.  

IRSF Scientific Symposium Oral Presentation Details

  • 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, April 26th at 3:45 PM Central Time
  • Rett Syndrome in Adulthood: The Caregiver Perspective
    Presenter – Kristin Phillips, Taysha Gene Therapies
    Date/Time – Wednesday, April 27th at 2:00 PM Central Time

ASCEND National Summit Oral Presentation Details

  • Putting Patients at the Center
    Presenters – Dr. Suyash Prasad, Taysha Gene Therapies and Emily McGinnis, Taysha Gene Therapies
    Date/Time – Thursday, April 28th at 12:45 PM Central Time

Additional details can be found at the IRSF Rett Syndrome Scientific Meeting website and the ASCEND Rett Syndrome National Summit 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.

Company Contact:
Kimberly Lee, D.O.
Chief Corporate Affairs Officer
Taysha Gene Therapies
klee@tayshagtx.com

Media Contact:
Carolyn Hawley
Canale Communications
carolyn.hawley@canalecomm.com


Taysha Gene Therapies, Inc.

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Biological Product (except Diagnostic) Manufacturing
Manufacturing
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United States of America
DALLAS

About TSHA

taysha gene therapies, inc., a gene therapy company, develops adeno-associated virus based gene therapies for the treatment of monogenic diseases of the central nervous system. it primarily develops tsha-101 for the treatment of gm2 gangliosidosis; tsha-118 for the treatment of cln1 disease; tsha-102 for the treatment of rett syndrome; tsha-103 for the treatment of slc6a1 haploinsufficiency disorder; and tsha-104 for the treatment for surfeit locus 1 deficiency. the company also has strategic partnership with the university of texas southwestern medical center to develop and commercialize transformative gene therapy treatments. taysha gene therapies, inc. was founded in 2019 and is based in dallas, texas.