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Safety and Efficacy of TSHA-102 in Pediatric Females With Rett Syndrome (REVEAL Pediatric Study)
Sponsor: Taysha Gene Therapies, Inc.
Summary
The REVEAL Pediatric Study is a multi-center, Phase 1/2 open-label, dose-escalation and dose-expansion study of TSHA-102, an investigational gene therapy, in pediatric females with Rett Syndrome. The safety, tolerability, and preliminary efficacy of two dose levels will be evaluated. The study duration is up to 6 years.
Official title: A Multicenter, Open Label, Randomized, Dose-Escalation and Dose-Expansion Study of the Safety, Tolerability, and Efficacy of a Single Intrathecal Administration of TSHA-102, an AAV9-Delivered Gene Therapy, for the Treatment of Pediatric Females With Rett Syndrome
Key Details
Gender
FEMALE
Age Range
5 Years - 8 Years
Study Type
INTERVENTIONAL
Enrollment
6
Start Date
2023-12-12
Completion Date
2031-11-02
Last Updated
2025-10-15
Healthy Volunteers
No
Conditions
Interventions
TSHA-102
TSHA-102 is a recombinant, non-replicating, self-complementary AAV9 (scAAV9) vector encoding for the miniMECP2 gene. TSHA-102 is a one-time intrathecal (IT) administration.
Locations (5)
Rush University Medical Center & Children's Hospital
Chicago, Illinois, United States
Gillette Children's Specialty Healthcare
Saint Paul, Minnesota, United States
Washington University, St. Louis
St Louis, Missouri, United States
CHU Ste-Justine
Montreal, Quebec, Canada
Children's Neurosciences, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust
London, United Kingdom