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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02716246




Registration number
NCT02716246
Ethics application status
Date submitted
17/03/2016
Date registered
23/03/2016

Titles & IDs
Public title
Phase I/II/III Gene Transfer Clinical Trial of scAAV9.U1a.hSGSH
Scientific title
Phase I/II/III Gene Transfer Clinical Trial of scAAV9.U1a.hSGSH for Mucopolysaccharidosis (MPS) IIIA
Secondary ID [1] 0 0
UX111-CL301
Secondary ID [2] 0 0
ABT001
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
MPS IIIA 0 0
Sanfilippo Syndrome 0 0
Sanfilippo A 0 0
Mucopolysaccharidosis III 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Other - ABO-102
Treatment: Drugs - Adjuvant Immunosuppression (IS) Therapy

Experimental: Cohort 1 Low Dose - Dose of 0.5 X 10\^13 vg/kg

Experimental: Cohort 2 Mid Dose - Dose of 1 X 10\^13 vg/kg

Experimental: Cohort 3 High Dose - Dose of 3 X 10\^13 vg/kg


Treatment: Other: ABO-102
Self-complementary adeno-associated virus serotype 9 carrying the human SGSH gene under the control of a U1a promoter (scAAV9.U1a.hSGSH) will be delivered one time through a venous catheter inserted into a peripheral limb vein.

Treatment: Drugs: Adjuvant Immunosuppression (IS) Therapy
The Principal Investigator and/or caregiver, in consultation with the medical monitor, will determine whether to initiate adjuvant IS therapy. Not all participants may receive IS therapy.
Intervention code [1] 0 0
Treatment: Other
Intervention code [2] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change from Baseline in Cognitive Domain Bayley Scales of Infant and Toddler Development Raw Scores-Third edition (BSID-III)
Timepoint [1] 0 0
Baseline, Up to Month 24
Secondary outcome [1] 0 0
Change From Baseline in Vineland Adaptive Behavior Scale II-Survey Interview Form
Timepoint [1] 0 0
Baseline, Up to Month 24
Secondary outcome [2] 0 0
Change From Baseline in Mullen Scales of Early Learning
Timepoint [2] 0 0
Baseline, Up to Month 24
Secondary outcome [3] 0 0
Change From Baseline in BSID-III: Language Domain
Timepoint [3] 0 0
Baseline, Up to Month 24
Secondary outcome [4] 0 0
Change From Baseline in BSID-III: Motor Domain
Timepoint [4] 0 0
Baseline, Up to Month 24
Secondary outcome [5] 0 0
Change From Baseline in KABC-II, if Applicable
Timepoint [5] 0 0
Baseline, Up to Month 24
Secondary outcome [6] 0 0
Change From baseline of Cerebrospinal Fluid (CSF) Heparan Sulfate After Treatment
Timepoint [6] 0 0
Baseline, Up to Month 24
Secondary outcome [7] 0 0
Change From Baseline in CSF Gangliosides [GM2-GM3]
Timepoint [7] 0 0
Baseline, Up to Month 24
Secondary outcome [8] 0 0
Change From Baseline in Brain Volumes After Treatment
Timepoint [8] 0 0
Baseline, Up to Month 24

Eligibility
Key inclusion criteria
* Diagnosis of MPS IIIA confirmed by the following methods:

* No detectable or significantly reduced SGSH enzyme activity by leukocyte assay, and
* Genomic DNA analysis demonstrating homozygous or compound heterozygous mutations in the SGSH gene
* Age: From birth to 2 years or children older than 2 years with a minimum cognitive Developmental Quotient (DQ) of 60 or above (calculated by Bayley Scales of lnfant and Toddler Development - Third Edition)
Minimum age
No limit
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Inability to participate in the clinical evaluation as determined by Principal Investigator (PI)
* Identification of two nonsense or null variants on genetic testing of the SGSH gene
* At least one S298P mutation in the SGSH gene
* Has evidence of an attenuated phenotype of MPS IIIA
* Presence of a concomitant medical condition that precludes lumbar puncture or use of anesthetics
* Active viral infection based on clinical observations
* Concomitant illness or requirement for chronic drug treatment that in the opinion of the PI creates unnecessary risks for gene transfer or precludes the child from participating in the protocol assessments and follow up
* Subjects with total anti-AAV9 antibody titers = 1:100 equivalent to a positive screen as determined by ELISA in serum
* Subjects with a positive response for the enzyme-linked immunosorbent spot (ELISpot) for T-cell responses to AAV9
* Serology consistent with exposure to HIV, or serology consistent with active hepatitis B or C infection
* Bleeding disorder or any other medical condition or circumstance in which a lumbar puncture (for collection of CSF) is contraindicated according to local institutional policy
* Visual or hearing impairment sufficient to preclude cooperation with neurodevelopmental testing
* Uncontrolled seizure disorder
* Any item (braces, etc.) which would exclude the subject from being able to undergo MRI according to local institutional policy
* Any other situation that precludes the subject from undergoing procedures required in this study
* Subjects with cardiomyopathy or significant congenital heart abnormalities
* The presence of significant non-MPS IlIA related CNS impairment or behavioral disturbances that would confound the scientific rigor or interpretation of results of the study
* Abnormal laboratory values Grade 2 or higher as defined in CTCAE v4.03 for GGT, total bilirubin, creatinine, hemoglobin, WBC count, platelet count, PT and aPTT
* Female participant who is pregnant or demonstrates a positive urine or bhCG result at screening assessment (if applicable)
* Any vaccination with viral attenuated vaccines less than 30 days prior to the scheduled date of treatment (and use of prednisolone)
* Previous treatment by Hematopoietic Stem Cell transplantation
* Previous participation in a gene/cell therapy or enzyme replacement therapy (ERT) clinical trial

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 2
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/03/2016
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/01/2025
Actual
Sample size
Target
Accrual to date
Final
28
Recruitment in Australia
Recruitment state(s)
SA
Recruitment hospital [1] 0 0
Women's and Children's Hospital - North Adelaide
Recruitment postcode(s) [1] 0 0
5006 - North Adelaide
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Ohio
Country [2] 0 0
United States of America
State/province [2] 0 0
Pennsylvania
Country [3] 0 0
Spain
State/province [3] 0 0
Barcelona
Country [4] 0 0
Spain
State/province [4] 0 0
Santiago De Compostela

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Ultragenyx Pharmaceutical Inc
Address
Country
Other collaborator category [1] 0 0
Commercial sector/industry
Name [1] 0 0
Abeona Therapeutics, Inc
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Medical Director
Address 0 0
Ultragenyx Pharmaceutical Inc
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
There is no plan to share data


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT02716246