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ACTIVE NOT RECRUITING
NCT06152237
PHASE1/PHASE2

Safety and Efficacy of TSHA-102 in Pediatric Females With Rett Syndrome (REVEAL Pediatric Study)

Sponsor: Taysha Gene Therapies, Inc.

View on ClinicalTrials.gov

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

GENETIC

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