Contact SCGE




Gene Therapy Trial Report

Summary

Gene Therapy With hLB-001 in Pediatric Patients With Severe Methylmalonic Acidemia


NCTID NCT04581785 (View at clinicaltrials.gov)
Description
Development Status Inactive
Indication Methylmalonic Acidemia
Disease Ontology Term DOID:0060740
Compound Name LB-001
Compound Description ALB-2A-MMUT
Sponsor LogicBio Therapeutics, Inc
Funder Type Industry
Recruitment Status
Terminated
Enrollment Count 4 (ACTUAL)
Results Posted View Results

Therapy Information


Target Gene/Variant MMUT
Therapy Type Gene transfer
Therapy Route In-vivo
Mechanism of Action Functional gene replacement
Route of Administration Intravenous
Drug Product Type Viral vector
Target Tissue/Cell Hepatocyte
Delivery System Viral transduction
Vector Type AAV-LK03
Dose 1 5E13 vg/kg
Dose 2 1E14 vg/kg

Study Record Dates


Current Stage Phase1, Phase2
Submit Date 2020-10-02
Completion Date 2023-01-10
Last Update 2024-02-23

Participation Criteria


Eligible Age 6 Months - 12 Years
Standard Ages Child
Sexes Eligible for Study ALL
Eligibility Criteria
Inclusion Criteria: * At the time of dosing, participants must be 6 months to 12 years of age * Males and females with diagnosis of severe MMA meeting all the following; 1. Isolated MMA with genetically confirmed, pathogenic mutations in the MMUT gene 2. Screening serum/plasma methylmalonic acid level of \>100 µmol/L 3. One or more of the following considered by the PI to be MMA-related: (i) An unscheduled ER visit, hospitalization or requirement for sick day diet in the year prior to screening visit (ii) Developmental delay, movement disorder, optic neuropathy or feeding disorder with tube feeding requirement 4. Medically stable for the 2 months prior to the start of screening Exclusion Criteria: * Participants with organic acidemias other than isolated MMA, or with any other causes of hyperammonemia * Having received MMA-targeted gene therapy or nucleic acid therapy * Participants on insulin or high dose hydroxocobalamin (\> 1 mg/day OHB12 parenteral) * Kidney or liver transplant, including hepatocyte cell therapy * Estimated glomerular filtration rate (eGFR) of \< 60 mL/min/1.73 m2 based on age appropriate equations, or ongoing dialysis for renal disease * Participant tests positive for anti-rAAV-LK03-neutralizing antibodies
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 4
Locations United States

Regulatory Information


Has US IND True
FDA Designations Fast Track, Orphan Drug Designation, Rare Pediatric Disease Designation
Recent Updates Program was terminated 4/25/23 due to low likelihood of clinical benefit

Resources/Links