- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02716246
Ensayo clínico de transferencia génica de fase I/II/III de scAAV9.U1a.hSGSH
Ensayo clínico de transferencia génica de fase I/II/III de scAAV9.U1a.hSGSH para mucopolisacaridosis (MPS) IIIA
The main objective of this study is to evaluate the efficacy and safety of UX111 for the treatment of MPS IIIA.
Descripción general del estudio
Estado
Descripción detallada
Open-label, single dose, dose-escalation clinical trial of UX111 (scAAV9.U1a.hSGSH) injected intravenously through a peripheral limb vein. A limited course of prophylactic immunomodulatory (IM) therapy will be administered. At approved sites adjuvant IM therapy may be administered to selected participants. The Principal Investigator and/or caregiver, in consultation with the medical monitor, will determine whether to initiate adjuvant IM therapy. Not all participants may receive adjuvant IM therapy.
This study was previously posted by Abeona Therapeutics, Inc and was transferred to Ultragenyx in August 2022.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Patients Contact: Trial Recruitment
- Número de teléfono: 1-888-756-8657
- Correo electrónico: trialrecruitment@ultragenyx.com
Copia de seguridad de contactos de estudio
- Nombre: HCPs Contact: Medical Information
- Número de teléfono: 1-888-756-8657
- Correo electrónico: medinfo@ultragenyx.com
Ubicaciones de estudio
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South Australia
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North Adelaide, South Australia, Australia, 5006
- Terminado
- Women's and Children's Hospital
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Santiago de Compostela, España, 15706
- Reclutamiento
- Hospital Clínico Universitario de Santiago
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Contacto:
- Eines Monteagudo, MD
- Correo electrónico: eines.monteagudo.vilavedra@sergas.es
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Investigador principal:
- Maria Luz Couce, MD
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Contacto:
- Beatriz Martín López-Pardo, MD
- Correo electrónico: beatriz.martin.lopezpardo@sergas.es
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Barcelona
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Barcelona, Barcelona, España, 08035
- Reclutamiento
- Vall d'Hebron Barcelona Hospital Campus
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Investigador principal:
- Mireia del Toro, MD
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Contacto:
- Mireia del Toro, MD
- Correo electrónico: mireia.deltoro@vallhebron.cat
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Ohio
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Columbus, Ohio, Estados Unidos, 43205
- Terminado
- Nationwide Children's Hospital
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Pennsylvania
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Pittsburgh, Pennsylvania, Estados Unidos, 15224
- Terminado
- Children's Hospital of Pittsburgh
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
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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 (based upon review of documented results from a qualified laboratory, and with confirmation with Medical Monitor)
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Age:
- For Cohort 1-3: From birth (participating sites in USA and Australia) OR 6 months (participating sites in Spain) to 2 years of age with no BSITD-III Cognitive Development Quotient (DQ) requirement, or older than 2 years with a BSITD-III Cognitive DQ of 60 or above (participating sites globally).
- For Cohort 4 (participating sites in Spain): 3 months to ≤ 2 years of age with no BSITD-III Cognitive DQ requirement or > 2 years of age with a BSITD-III Cognitive DQ ≥ 60 (n = up to 6). Up to 2 additional subjects > 2 years and ≤ 5 years of age with a BSITD-III Cognitive DQ < 60 may also be enrolled. •Subjects must be ≥ 6 months of age before UX111 administration. However, subjects may be consented and initiate relevant Screening Procedures and IM treatment < 6 months of age. Refer to Section 8.2 for relevant screening procedures •For children ≤ 24 months chronological age who were born prematurely, defined as born at < 36 weeks gestational age, the corrected gestational age must be used for determining inclusion •The BSITD-III Cognitive DQ is assessed during the onsite Screening visit, for subjects who require it •The age of the child on the date of the Screening BSITD-III assessment is used to determine the requirement for the BSITD-III Cognitive DQ score.
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Cohort 4 only: Vaccination status based on age according to country-specific guidelines that is up to date 30 days prior to Enrollment as verified by documentation from the subject's primary care physician, and willing to defer vaccines through 6 months after completion of the subject's IM medication, or longer per Principal Investigator (PI) judgment. Emergency use authorization or conditional marketing authorization of coronavirus disease (COVID) vaccines is included unless there is an accepted medical exemption.
Exclusion Criteria:
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Inability to participate in the clinical evaluation as determined by PI
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Cohorts 1 to 3 only: Identification of two nonsense or null variants on genetic testing of the SGSH gene (based upon review of documented results from a qualified laboratory, and with confirmation with Medical Monitor)
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At least one S298P mutation in the SGSH gene (based upon review of documented results from a qualified laboratory, and with confirmation with Medical Monitor)
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Has evidence of an attenuated phenotype of MPS IIIA, in the judgement of the PI
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Presence of a concomitant medical condition that precludes lumbar puncture or use of anesthetics
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Active viral infection based on clinical observations
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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
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Cohorts 1 to 3 only: Subjects with total anti-AAV9 antibody titers ≥ 1:100 equivalent to a positive screen as determined by ELISA binding assay in serum
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Cohorts 1-3 only: Subjects with a positive response for the enzyme-linked immunosorbent spot assay (ELISpot) for T-cell responses to AAV9
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Cohorts 1-3 only: Serology consistent with exposure to human immunodeficiency virus (HIV), or serology consistent with active hepatitis B or C infection, Cohort 4: Current clinically significant infections (including any requiring systemic treatment including, but not limited to, HIV; hepatitis A, B, or C; varicella zosters virus; human T-cell lymphotropic virus type 1 [HTLV-1]; tuberculosis; or COVID-19) that would interfere with participation in the study.
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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
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Visual, hearing, or other impairment sufficient to preclude cooperation with neurodevelopmental testing
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Uncontrolled seizure disorder
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Any item (braces, etc.) or circumstance that would exclude the subject from being able to undergo MRI according to local institutional policy
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Any other situation that precludes the subject from undergoing procedures required in this study
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Subjects with cardiomyopathy or significant congenital heart abnormalities
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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
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Cohorts 1-3: Abnormal laboratory values Grade 2 or higher as defined in common terminology criteria for adverse events (CTCAE) v4.03 for gamma-glutamyl transferase (GGT), total bilirubin, creatinine, hemoglobin, white blood cell (WBC) count, platelet count, prothrombin time (PT) and activated partial thromboplastin time (aPTT), Cohort 4: Any of the following abnormal laboratory values from screening assessment:
- Aspartate aminotransferase (AST), alanine aminotransferase (ALT), GGT, and/or alkaline phosphatase ≥ 2 × upper limit of normal (ULN) and/or total bilirubin > 1.5 × ULN
- Anemia (hemoglobin < 10 g/dL)
- Leukopenia or leukocytosis (total WBC count < 3,000/mm3 and > 15,000/mm3 respectively)
- Abnormal absolute neutrophil count (ANC) of < 1000/mm3
- Platelet count < 100,000/mm3
- Coagulopathy (international normalized ratio [INR] > 1.5) or aPTT > 40 seconds
- Renal impairment, defined as estimated glomerular filtration rate (eGFR) below the lower limit of normal (age and sex appropriate) based on Bedside Schwartz equation
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Female of childbearing potential who is pregnant or demonstrates a positive urine or bhCG result at screening assessment (if applicable)
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Cohorts 1-3: Any vaccination with viral attenuated vaccines less than 30 days prior to the scheduled date of treatment (and use of prednisolone)
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Previous treatment by hematopoietic stem cell transplantation
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Previous participation in a gene/cell therapy or enzyme replacement therapy (ERT) clinical trial
Cohort 4 only:
- Known hypersensitivity, that in the judgment of the PI, places the subject at increased risk for adverse effects.
- Unwilling to avoid consumption of grapefruit juice and the use of strong inhibitors of CYP3A4 and/or P-gp (eg, ketoconazole, voriconazole, itraconazole, erythromycin, telithromycin, or clarithromycin), strong inducers of CYP3A4 and/or P-gp (eg, rifampin, rifabutin, phenobarbital, carbamazepine, or phenytoin), and St. John's Wort from 30 days prior to Screening through completion of the IM regimen.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Cohort 1 Low Dose
Dose of 0.5 X 10^13 vg/kg |
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.
Otros nombres:
The Principal Investigator and/or caregiver, in consultation with the medical monitor, will determine whether to initiate adjuvant IM therapy. Not all participants may receive adjuvant IM therapy. |
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Experimental: Cohort 2 Mid Dose
Dose of 1 X 10^13 vg/kg |
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.
Otros nombres:
The Principal Investigator and/or caregiver, in consultation with the medical monitor, will determine whether to initiate adjuvant IM therapy. Not all participants may receive adjuvant IM therapy. |
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Experimental: Cohort 3 High Dose
Dose of 3 X 10^13 vg/kg |
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.
Otros nombres:
The Principal Investigator and/or caregiver, in consultation with the medical monitor, will determine whether to initiate adjuvant IM therapy. Not all participants may receive adjuvant IM therapy. |
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Experimental: Cohort 4 High Dose (Spain Only)
Dose of 3 X 10^13 vg/kg |
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.
Otros nombres:
The Principal Investigator and/or caregiver, in consultation with the medical monitor, will determine whether to initiate adjuvant IM therapy. Not all participants may receive adjuvant IM therapy. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Cerebrospinal Fluid (CSF) Heparan Sulfate (HS) (Disaccharide) Exposure
Periodo de tiempo: Up to Month 24 Visit
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Exposure is defined as the time-normalized area under the curve (AUC) of the percentage reduction from baseline. |
Up to Month 24 Visit
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Cambio porcentual desde el inicio en LCR HS
Periodo de tiempo: Visita inicial, hasta el mes 24
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Visita inicial, hasta el mes 24
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Cambio porcentual desde el inicio en el volumen cortical total
Periodo de tiempo: Visita inicial, hasta el mes 24
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Visita inicial, hasta el mes 24
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Escalas Bayley de desarrollo de bebés y niños pequeños, tercera edición (BSITD-III), puntuación bruta cognitiva a lo largo del tiempo
Periodo de tiempo: Hasta el mes 24 Visita
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Hasta el mes 24 Visita
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Puntuación bruta de comunicación receptiva de BSITD-III a lo largo del tiempo
Periodo de tiempo: Hasta el mes 24 Visita
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Hasta el mes 24 Visita
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Puntuación bruta de comunicación expresiva de BSITD-III a lo largo del tiempo
Periodo de tiempo: Hasta el mes 24 Visita
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Hasta el mes 24 Visita
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CSF Ganglioside Type 2 (GM2) Exposure
Periodo de tiempo: Up to Month 24 Visit
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Exposure is defined as the time-normalized area under the curve (AUC) of the percentage change from baseline. |
Up to Month 24 Visit
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CSF Ganglioside Type 3 (GM3) Exposure
Periodo de tiempo: Up to Month 24 Visit
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Exposure is defined as the time-normalized area under the curve (AUC) of the percentage change from baseline. |
Up to Month 24 Visit
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Otras medidas de resultado
Medida de resultado |
Periodo de tiempo |
|---|---|
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Número de participantes con eventos adversos surgidos del tratamiento y eventos adversos graves surgidos del tratamiento
Periodo de tiempo: Hasta el mes 24 Visita
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Hasta el mes 24 Visita
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Director de estudio: Medical Director, Ultragenyx Pharmaceutical Inc
Publicaciones y enlaces útiles
Publicaciones Generales
- Fu H, Meadows AS, Pineda RJ, Kunkler KL, Truxal KV, McBride KL, Flanigan KM, McCarty DM. Differential Prevalence of Antibodies Against Adeno-Associated Virus in Healthy Children and Patients with Mucopolysaccharidosis III: Perspective for AAV-Mediated Gene Therapy. Hum Gene Ther Clin Dev. 2017 Dec;28(4):187-196. doi: 10.1089/humc.2017.109. Epub 2017 Oct 24.
- McCurdy VJ, Johnson AK, Gray-Edwards HL, Randle AN, Bradbury AM, Morrison NE, Hwang M, Baker HJ, Cox NR, Sena-Esteves M, Martin DR. Therapeutic benefit after intracranial gene therapy delivered during the symptomatic stage in a feline model of Sandhoff disease. Gene Ther. 2021 Apr;28(3-4):142-154. doi: 10.1038/s41434-020-00190-1. Epub 2020 Sep 3.
- Fu H, Cataldi MP, Ware TA, Zaraspe K, Meadows AS, Murrey DA, McCarty DM. Functional correction of neurological and somatic disorders at later stages of disease in MPS IIIA mice by systemic scAAV9-hSGSH gene delivery. Mol Ther Methods Clin Dev. 2016 Jun 8;3:16036. doi: 10.1038/mtm.2016.36. eCollection 2016.
Enlaces Útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimado)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Metabolismo, errores congénitos
- Enfermedades Genéticas Congénitas
- Enfermedades metabólicas
- Enfermedades del tejido conectivo
- Metabolismo de carbohidratos, errores congénitos
- Enfermedades de almacenamiento lisosomal
- Mucinosis
- Mucopolisacaridosis
- Enfermedades y anomalías congénitas, hereditarias y neonatales
- Enfermedades Nutricionales y Metabólicas
- Enfermedades de la piel y del tejido conectivo
- Mucopolisacaridosis III
- Terapéutica
Otros números de identificación del estudio
- ABT-001
- UX111-CL301 (Otro identificador: Ultragenyx Pharmaceutical Inc)
- 2015-003904-21 (Número EudraCT)
- 2023-510032-37-00 (Ctis)
- 2023 (Subvención/contrato del NIH de EE. UU.)
- 2015 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .