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Gene Therapy Trial Report

Summary

Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)


NCTID NCT00494195 (View at clinicaltrials.gov)
Description
Development Status Inactive
Indication Limb-Girdle Muscular Dystrophy, Type 2D/R3
Disease Ontology Term DOID:0110278
Compound Name RAAV1.tMCK.human-alpha-sarcoglycan
Sponsor Nationwide Children's Hospital
Funder Type Other
Recruitment Status
Completed
Enrollment Count 6 (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 Intramuscular (extensor digitorum brevis)
Drug Product Type Viral vector
Target Tissue/Cell Muscle
Delivery System Viral transduction
Vector Type AAV1
Dose 1 3.25E11 vg

Study Record Dates


Current Stage Phase1
Submit Date 2007-06-27
Completion Date 2011-08
Last Update 2013-02-05

Participation Criteria


Eligible Age >=5 Years
Standard Ages Child, Adult, Older adult
Sexes Eligible for Study ALL
Eligibility Criteria
Inclusion Criteria: * Six LGMD2D subjects ages 5 and older based on the clinical degree of involvement (impaired muscle function/weakness, sufficient muscle preservation) * Preservation of EDB muscle or another muscle if judged more favorable because of adequate muscle mass for gene transfer * Males and females of any ethnic group * Established mutations of an -SG gene on both alleles * Ability to cooperate for testing * Sexually active patients must be willing to practice a reliable method of contraception during the study Exclusion Criteria: * Active viral infection (symptoms listed in section 9.0 of the protocol) * LGMD2D subjects without weakness or functional loss * Cardiomyopathy based on clinical exam and ECHO with ejection fraction less than 40% * HIV infected * Hepatitis A, B, or C infected * Autoimmune diseases and immunosuppressive drugs (other than pulse methylprednisolone at time of gene transfer) * Persistent leucopenia or leucocytosis (WBC less than or equal to 3.5 K/cu mm or at least 20.0 K/ cu mm) or neutrophils less than 1.5 K/ cu mm * Concomitant illness or requirement for chronic drug treatment that in the opinion of the Principal Investigator creates unnecessary risks for gene transfer * Pregnancy * Abnormal laboratory values considered clinically significant * Alcoholism (CAGE questionnaire), and laboratory tests such as GGT and MCV
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
Recent Updates Study drug was well tolerated by 3/3 subjects, protein was detectable in all subjects at 6 months post-injection. Clinical development of this program moved to Sarepta Therapeutics with optimized AAV capsid and modified intramuscular delivery

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