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Gene Therapy Trial Report

Summary

ATA-200 Gene Therapy Trial in Patients With LGMDR5


NCTID NCT05973630 (View at clinicaltrials.gov)
Description
Development Status Active
Indication Limb-Girdle Muscular Dystrophy, Type 2C/R5
Disease Ontology Term DOID:0110277
Compound Name ATA-200
Sponsor Atamyo Therapeutics
Funder Type Industry
Recruitment Status
Active not recruiting
Enrollment Count 4 (ACTUAL)
Results Posted Not Available

Therapy Information


Target Gene/Variant SGCG
Therapy Type Gene transfer
Therapy Route In-vivo
Mechanism of Action Functional gene replacement
Route of Administration Intravenous
Drug Product Type Viral vector
Delivery System Viral transduction
Vector Type AAV2/8
Editor Type none
Dose 1 1.0E14 vg/kg
Dose 2 3.0E14 vg/kg

Study Record Dates


Current Stage Phase1
Submit Date 2023-07-24
Completion Date 2031-01-31
Last Update 2026-01-29

Participation Criteria


Eligible Age 6 Years - 13 Years
Standard Ages Child
Sexes Eligible for Study ALL
Eligibility Criteria
Inclusion Criteria: * Confirmed diagnosis of LGMDR5 before age of 10, based on clinical presentation and genotyping * Ambulant male or female patients aged 6 to less than 12 years of age at screening * Able to perform the 10-meter walk test (10MWT) in less than 15 sec and to rise from chair with or without arm support Exclusion Criteria: * Detectable neutralizing antibodies against AAV8 * Cardiomyopathy with left ventricular ejection fraction (LVEF) \< 50% * Respiratory assistance * Concomitant medical condition that might interfere with LGMDR5 evolution * Acute illness within 4 weeks of anticipated IMP administration * Current participation in another clinical trial with investigational medicinal product * Previous participation in gene and cell therapy trials * Any condition that would contraindicate immunosuppressant treatment * Presence of any permanent items (e.g., metal braces) precluding undergoing MRI * Any vaccination 1 month prior to planned IMP administration * Serology consistent with HIV exposure or active hepatitis B or C infection * Grade 2 or higher lab abnormalities for liver function tests, creatinine, hemogram and coagulation
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 1
Locations United States

Regulatory Information


Has US IND True
FDA Designations Orphan Drug Designation, Rare Pediatric Disease Designation
Recent Updates New results posted March 2026

Resources/Links