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RGX-121 Gene Therapy in Children 5 Years of Age and Over With MPS II (Hunter Syndrome)
Bu çalışma, MPS II (Hunter sendromu, Hunter syndrome) hastalığı olan çocuklarda RGX-121 adlı gen terapisinin güvenliliğini incelemektedir. Çalışmaya, IDS genindeki mutasyonlara bağlı nöronopatik forma sahip olduğu belgelenmiş, 5 yaş ve üzeri çocuklar dahil edilmiştir. Çalışma Faz 1/Faz 2 aşamasında yürütülmüş ve tamamlanmıştır.
Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.
Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.
Inclusion Criteria: Meets any of the following criteria: 1. Has a documented diagnosis of MPS II AND a neurocognitive testing score ≤ 1 ½ standard deviation (SD) from the test normative mean (BSID-III: 77 and MSEL Visual Reception: 35), OR 2. Has a documented diagnosis of MPS II AND has a decline of ≥ 1 standard deviation on serial neurocognitive testing administered between 3 to 36 months apart (BSID-III Cognitive or MSEL Visual Reception), OR 3. Has a relative clinically diagnosed with neuronopathic MPS II who has the same IDS mutation as the participant AND the participant in the opinion of a geneticist has inherited a neuronopathic form of MPS II, OR 4. Has documented mutation(s) in IDS that in the opinion of a geneticist is known to result in a neuronopathic phenotype AND in the opinion of a clinician has a neuronopathic form of MPS II Exclusion Criteria: 1. Has contraindications for intracisternal injection, intracerebroventricular injection, or lumbar puncture 2. Has contraindications for immunosuppressive therapy 3. Has any neurocognitive deficit not attributable to MPS II or diagnosis of a neuropsychiatric condition 4. Has had prior treatment with an AAV-based gene therapy product 5. If receiving ELAPRASE® via intrathecal (IT) administration, must agree to discontinue IT idursulfase for the duration of the study 6. Has experienced a serious hypersensitivity reaction to intravenous (IV) ELAPRASE® 7. Is currently failing to respond to idursulfase (ELAPRASE®) IV due to neutralizing anti-idursulfase antibodies 8. Has received any investigational product within 30 days of Day 1 or 5 half-lives before signing of the ICF, whichever is longer 9. Has a platelet count \<100,000 per microliter (µL), absolute neutrophil count \<1.0 × 103/µL, or aminotransferase (ALT) or aspartate aminotransferase (AST) \>3 × upper limit of normal (ULN) or total bilirubin \>1.5 × ULN at screening unless the participant has a previously known history of Gilbert's syndrome