Raav2/5-hnaglu    (DrugBank: -)

1 disease
IDDisease name (Link within this page)Number of trials
19Lysosomal storage disease2

19. Lysosomal storage disease    [ 784 clinical trials,   673 drugs,   (DrugBank: 101 drugs),   68 drug target genes,   184 drug target pathways]
Searched query = "Lysosomal storage disease", "Lysosomal disease", "Gaucher disease", "Niemann-Pick disease", "Niemann-Pick type C", "GM1-gangliosidosis", "GM1-ganglio ... show all
The queries were searched in Public_title, Scientific_title, and Condition. Export date: 03/15/2021. Trials are sorted by Date_enrollment from most recent to oldest in the table.
2 / 784 trials found
No.TrialIDDate_
enrollment
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registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
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Inclusion_
agemin
Inclusion_
agemax
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PhaseCountries
1NCT03300453
(ClinicalTrials.gov)
September 17, 201315/6/2016Intracerebral Gene Therapy in Children With Sanfilippo Type B SyndromeProtocol AMT110-CD-001: A Phase I/II, Open-label, Study of Intracerebral Administration of Adeno-associated Viral Vector Containing the Human Alpha-N-acetylglucosaminidase cDNA in Children With Sanfilippo Type B SyndromeSanfilippo Syndrome BDrug: rAAV2/5-hNAGLUUniQure Biopharma B.V.Venn Life Sciences;Institut PasteurCompleted18 Months60 MonthsAll4Phase 1;Phase 2France
2EUCTR2012-000856-33-FR
(EUCTR)
15/05/2014Intracerebral Gene therapy in children with Sanfilippo type B syndromeA phase I/II, open-label, study of intracerebral administration of adeno-associated viral vector containing the human alpha-N-acetylglucosaminidase cDNA in children with Sanfilippo type B syndrome Mucopolysaccharidosis III B
MedDRA version: 17.0;Level: PT;Classification code 10056890;Term: Mucopolysaccharidosis III;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Body processes [G] - Genetic Phenomena [G05]
Product Name: rAAV2/5-hNaGluInstitut PasteurNULLNAFemale: yes
Male: yes
Phase 1;Phase 2France