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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
Dose 1 1.0E14 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 May 2026 on 4 patients, including 12 months of follow-up on first 2 patients treated

Resources/Links