SNPMiner Trials by Shray Alag
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SNPMiner Trials (Home Page)
Report for Mutation R447H
Developed by Shray Alag, 2020.
SNP Clinical Trial Gene
There is one clinical trial.
Clinical Trials
1 Direct CNS Administration of a Replication Deficient Adeno-associated Virus Gene Transfer Vector Serotype rh.10 Expressing the Human CLN2 cDNA to Children With Late Infantile Neuronal Ceroid Lipofuscinosis (LINCL)
This is a proposed follow up study on the investigators previous gene transfer human clinical trial entitled "Administration of a Replication Deficient Adeno-associated Virus Gene Transfer Vector Expressing the Human CLN2 cDNA to the Brain of Children with Late Infantile Neuronal Ceroid Lipofuscinosis" (Weill Cornell IRB# 0401007010). As in the previous study, the investigators propose to administer a biologic by direct gene transfer into the brain and assess its safety on children with a fatal genetic disease of the central nervous system (CNS). The disease is Late Infantile Neuronal Ceroid Lipofuscinosis (LINCL, a form of Batten disease). This will be accomplished by using delivery of a gene (method called gene transfer) to administer to the brain an experimental drug called AAVRh.10CUhCLN2, a gene transfer vector.
NCT01161576 Conditions
- Batten Disease
- Late-Infantile Neuronal Ceroid Lipofuscinosis
Interventions
- Biological: AAVrh.10CUhCLN2 vector 9.0x10^11 genome copies
- Biological: AAVrh.10CUhCLN2 vector 2.85x10^11 genome copies
MeSH:Neuronal Ceroid-Lipofuscinoses
If either parental allele is R447H, the patient will not be included in the study. --- R447H ---
Primary Outcomes
Description: A clinical rating, 12 point scale which combines assessment of feeding, gait, motor and language to give an overall assessment of various CNS functions.
Measure: Change in Weill-Cornell LINCL scale from Baseline to 18 months Time: 18 MonthsDescription: Based on previous analyses, we have determined that 3 imaging parameters (% grey matter volume, MRI Assessment, % ventricular volume and cortical apparent diffusion coefficient) correlate best with age and with the Weill Cornell LINCL scale and will be used to assess disease progression and the effect of the gene transfer.
Measure: Disease progression based on change in MRI imaging parameter (% grey matter volume) from Baseline to 18 Months Time: 18 MonthsDescription: Based on previous analyses, we have determined that 3 imaging parameters (% grey matter volume, MRI Assessment, % ventricular volume and cortical apparent diffusion coefficient) correlate best with age and with the Weill Cornell LINCL scale and will be used to assess disease progression and the effect of the gene transfer.
Measure: Disease progression based on change in MRI imaging parameter (% ventricular volume) from Baseline to 18 Months Time: 18 MonthsDescription: Based on previous analyses, we have determined that 3 imaging parameters (% grey matter volume, MRI Assessment, % ventricular volume and cortical apparent diffusion coefficient) correlate best with age and with the Weill Cornell LINCL scale and will be used to assess disease progression and the effect of the gene transfer.
Measure: Disease progression based on change in MRI imaging parameter cortical apparent diffusion coefficient) from Baseline to 18 Months Time: 18 MonthsSecondary Outcomes
Description: The quality of life survey that will be completed by at least one parent/legal guardian at the screening visit and the month 18 visit will be either the Infant Toddler Quality of Life (ITQoL) questionnaire or the Child Health Questionnaire (CHQ), depending on the age of the subject. The ITQoL is administered to subjects up to the age of five and the CHQ is administered to subjects from age 5-18.
Measure: Change in Quality of Life Survey from Baseline to 18 Months Time: 18 monthsDescription: Averaging the scores from the Mullen Scale
Measure: Mullen Scale (developmental assessment) from Baseline to 18 Months Time: 18 months