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This study examines a gene therapy that uses the patient's own stem cells (autologous hematopoietic stem cells) modified to carry the IDS gene, in patients with mucopolysaccharidosis type II (Hunter syndrome). It enrolls male infants aged 3-22 months with the severe (progressive neuronopathic) form of the disease. The study is in Phase 1/Phase 2 and is currently active but not recruiting participants.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: 1. Written informed consent from a legally authorized guardian. 2. Male, age at consent ≥3 months and ≤22 months. 3. Normal cognitive function or mild cognitive dysfunction (patient has a Development Quotient (DQ) score ≥70 at screening as determined by the Bayley Scale of Infant Development-third edition (BSID-III), cognitive domain), or assessed as normal or only mildly impaired by experienced neuropsychologist. 4. Close male relative with known severe (progressive neuronopathic) phenotype of MPSII, or genotype associated with progressive neuronopathic phenotype. This is to be confirmed by the independent expert reviewers. 5. IDS activity ≤10% of the Lower Limit of Normal as measured in leucocytes or plasma, plus either (1) a normal enzyme activity level of at least one other sulfatase (to rule out multiple sulfatase deficiency) as measured in leucocytes, or (2) a documented mutation in the IDS gene. 6. Medically stable and able to accommodate the protocol requirements, including travel without placing an undue burden on the patient/patient's family, as determined by the CI. 7. Patients and their parents/legal guardians must be willing and able to comply with study restrictions and to commit to attend clinic for the required duration during the study and follow-up period as specified in the protocol. Exclusion Criteria: 1. The patient has previously received stem cell or gene therapy 2. The patient has received modified intravenous ERT or intra-thecal ERT in a trial setting. 3. Patient currently enrolled in another interventional clinical trial 4. The patient has a history of poorly controlled seizures 5. Hemizygous for mutation known to be associated with non-neuropathic phenotype 6. The patient is currently receiving psychotropic or other medications which, in the CI's opinion, would be likely to substantially confound test results 7. The patient has received any investigational medicinal product (including Genistein) within 30 days prior to the Baseline visit or is scheduled to receive any investigational medicinal product during the course of the study 8. Documented Human Immunodeficiency Virus (HIV) infection (positive HIV RNA and/or anti-p24 antibodies) 9. Malignant neoplasia (except local skin cancer) or a documented history of hereditary cancer syndrome. Patients with a prior successfully treated malignancy and a sufficient follow-up to exclude recurrence (based on oncologist opinion) can be included after discussion and approval by the Medical Monitor 10. Myelodysplasia, cytogenetic alterations characteristic of myelodysplastic syndrome and acute myeloid leukaemia, or other serious haematological disorders 11. The patient has a medical condition or extenuating circumstance that, in the opinion of the CI, might compromise the patient's ability to comply with protocol requirements, the patient's well-being or safety, or the interpretability of the patient's clinical data 12. Visual or hearing impairment sufficient to preclude adequate neurodevelopmental testing 13. Severe behavioural disturbances due to reasons other than MPS II and likely to interfere with protocol compliance, as determined by the CI 14. Known sensitivity to Busulfan 15. The receipt of live vaccinations within 30 days prior to treatment start 16. Known sensitivity to DMSO