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Gene Therapy Trial Report

Summary

Study to Evaluate the Safety, Tolerability, and Efficacy of SRP-9004 Administered by Systemic Infusion in Limb Girdle Muscular Dystrophy Type 2D/R3 Participants in the United States


NCTID NCT06747273 (View at clinicaltrials.gov)
Description
Development Status Inactive
Indication Limb-Girdle Muscular Dystrophy, Type 2D/R3
Disease Ontology Term DOID:0110278
Compound Name SRP-9004
Compound Alias Patidistrogene bexoparvovec
Compound Description rAAVrh74-tMCK-SGCA
Sponsor Sarepta Therapeutics, Inc.
Funder Type Industry
Recruitment Status
Terminated
Enrollment Count 4 (ACTUAL)
Results Posted Not Available

Therapy Information


Target Gene/Variant SGCA
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 AAVrh74
Editor Type none
Dose 1 Phase 1/2 study: 1E12 vg/kg/single limb (n=1)
Dose 2 Phase 1/2 study: 1E12 vg/kg/limb (n=3), total dose: 2E12 vg/kg
Dose 3 Phase 1/2 study: 3E12 vg/kg/limb (n=2), total dose: 6E12 vg/kg

Study Record Dates


Current Stage Phase1
Submit Date 2024-12-18
Completion Date 2025-06-18
Last Update 2025-09-04

Participation Criteria


Eligible Age >=4 Years
Standard Ages Child, Adult, Older adult
Sexes Eligible for Study ALL
Eligibility Criteria
Key Inclusion Criteria: * Ambulatory participants, defined as able to walk without assistive aid, 10MWR \<30 seconds, and NSAD total score ≥25; non-ambulatory participant, defined as 10MWR ≥30 seconds or unable to perform, and PUL 2.0 entry scale score ≥3. * Ambulatory participants must be 4 to 20 years of age and the non-ambulatory participant must be ≥4 years of age. * All participants must be ≤70 kilograms * Possess 1 homozygous or 2 heterozygous pathogenic and/or likely pathogenic α-SG deoxyribonucleic acid (DNA) gene mutations as documented prior to screening. * Able to cooperate with muscle testing. * Participants must have adeno-associated virus (AAV) serotype Rh74 (rh74) antibody titers \<1:400 (that is, not elevated) as determined by an enzyme-linked immunosorbent assay (ELISA). Key Exclusion Criteria: * Left ventricular ejection fraction \<40% or clinical signs and/or symptoms of cardiomyopathy * FVC ≤40% of predicted value and/or requirement for nocturnal ventilation * Any other clinically significant illness, including neuromuscular (other than limb girdle muscular dystrophy type 2D/R3 \[LGMD2D/R3\]), that in the opinion of the Investigator might compromise the participant's ability to comply with the protocol required testing or procedures or compromise the participant's wellbeing, safety, or clinical interpretability. Other inclusion/exclusion criteria apply.
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 2
Locations United States

Regulatory Information


Has US IND True
FDA Designations Orphan Drug Designation
Recent Updates Placed on clinical hold due to patient death, Sarepta announced they were pausing this program as part of a strategic restructuring

Resources/Links