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Gene Therapy Trial Report

Summary

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


NCTID NCT06152237 (View at clinicaltrials.gov)
Description
Development Status Active
Indication Rett Syndrome
Disease Ontology Term DOID:1206
Compound Name TSHA-102
Sponsor Taysha Gene Therapies, Inc.
Funder Type Industry
Recruitment Status
Active not recruiting
Enrollment Count 6 (ACTUAL)
Results Posted Not Available

Therapy Information


Target Gene/Variant MiniMECP2
Therapy Type Gene transfer
Therapy Route In-vivo
Mechanism of Action Functional gene replacement
Route of Administration Intrathecal
Drug Product Type Viral vector
Delivery System Viral transduction
Vector Type scAAV9
Editor Type none
Dose 1 5.7E14 vg
Dose 2 1E15 vg

Study Record Dates


Current Stage Phase1, Phase2
Submit Date 2023-11-21
Completion Date 2031-11-02
Last Update 2025-10-15

Participation Criteria


Eligible Age 5 Years - 8 Years
Standard Ages Child
Sexes Eligible for Study FEMALE
Eligibility Criteria
Inclusion Criteria: * Participant has a confirmed diagnosis of classical/typical Rett Syndrome with a documented mutation of the MECP2 gene that results in loss of function. * Participant is between ≥5 to ≤8 years of age at the time of consent. * Participant must be up to date with all relevant local vaccination requirements, with last vaccination dose received at least 42 days prior to the start of the immunosuppression regimen. * Participant's parent/caregiver must be willing to allow participant to receive blood or blood products for the treatment of an AE if medically needed. Exclusion Criteria: * Participant has another neurodevelopmental disorder independent of the MECP2 gene loss of function mutation, or any other genetic syndrome with a progressive course. * Participant has a history of brain injury that causes neurological problems. * Participant had grossly abnormal psychomotor development in the first 6 months of life. * Participant has a diagnosis of atypical Rett syndrome. * Participant has an MECP2 mutation that does not cause Rett syndrome. * Participant requires non-invasive and invasive ventilatory support. * Participant has contraindications for IT administration of TSHA-102 or lumbar puncture procedure, other medical conditions, or contraindications to any medications required for IT administration. * Participant has acute or chronic hepatitis B or C infections.
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 5
Locations Canada,United States,United Kingdom

Regulatory Information


Has US IND True
FDA Designations Breakthrough Therapy, Fast Track, Orphan Drug Designation, Rare Pediatric Disease Designation, Regenerative Medicine Advanced Therapy
Recent Updates Dosing of the first patient in the pivotal trial is expected 4Q25

Resources/Links