- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07605429
BEACON - Phase III Clinical Study of Rugonersen in Angelman Syndrome. (BEACON)
A Randomized, Multi-center, Double-blind, Sham-controlled, Phase III Clinical Study to Evaluate the Efficacy and Safety of Intrathecally Administered Rugonersen in Pediatric and Adult Participants With Angelman Syndrome
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 3
Acceso ampliado
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Brenda Vincenzi, MD
- Número de teléfono: +1 857 855 4107
- Correo electrónico: beaconstudy@mytomorrows.com
Ubicaciones de estudio
-
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California
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San Diego, California, Estados Unidos, 92123
- Reclutamiento
- Rady Children's Hospital
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Investigador principal:
- Lynne Bird
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Illinois
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Chicago, Illinois, Estados Unidos, 60612
- Reclutamiento
- Rush University
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Investigador principal:
- Elizabeth Berry-Kravis
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North Carolina
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Chapel Hill, North Carolina, Estados Unidos, 27510
- Reclutamiento
- University of North Carolina at Chapel Hill School of Medicine
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Investigador principal:
- Elizabeth Jalazo
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Male or female and ≥ 1 year to ≤ 50 years of age at signing of the informed consent form.
Independent of the age of the participant, the participant has a parent, caregiver or legal representative (herein after referred to as caregiver) who is reliable and competent in the Investigator's judgement. The caregiver is:
- Able to consent for the participant according to ICH and local regulations,
- At least 18 years of age,
- Willing and able to accompany the participant to clinic visits and be available to the investigational site by telephone, email, or other electronic form as needed,
- Is, and will likely remain, sufficiently knowledgeable of participant's condition throughout the study to be able to respond to queries, and is willing and able to complete caregiver assessments and inform the site personnel about the participant's condition as requested.
- Clinical diagnosis of Angelman syndrome.
Pre-existing medical records confirm the clinical diagnosis of AS and the molecular diagnosis with genotypic classification of either:
- Mutation in the UBE3A gene, and the pathogenic or likely pathogenic variant identified,
- Deletion on the maternally inherited chromosome 15q11-q13 that encompasses the UBE3A gene.
- Able to comply with all study requirements.
- Able to tolerate blood draws.
- Able to undergo LP and IT injection, under sedation or anesthesia without intubation as deemed appropriate.
- Has stable medical status for at least 4 weeks prior to screening and at the time of enrolment.
- Bodyweight > 7.5 kg
- Legally authorized representative/caregiver(s) agree(s) not to share any of the participant's personal medical data or information related to the study by any means, including, e.g., a website or a post on a social media site (e.g., Facebook, Instagram, Twitter, YouTube, TikTok, etc.) from the time of enrollment until they are notified that the study is completed.
- Stable permitted medications (including cannabidiol [CBD]) for epilepsy for 12 weeks prior to screening and at the time of enrolment, with the exception of age/weight-based or blood level (toxicity) dose adjustments.
- Stable concurrent psychotropic medications for 4 weeks prior to screening and at time of enrolment.
- Complies with the requirements regarding contraception and is confirmed by caregiver consent.
Exclusion Criteria:
Molecular diagnosis of AS with genotypic classification of:
- Uniparental paternal disomy (UPD) of 15q11-q13,
- Imprinting center defect (ICD) within 15q11-q13,
- A partial molecular diagnosis of AS, that cannot exclude UPD or ICD despite appropriate genetic testing.
Clinically significant vital signs or laboratory abnormalities during screening, including:
o Abnormal coagulation profile demonstrated by platelet count at or below lower limit of normal (140 × 109/L), or by abnormal international normalized ratio (INR) and/or prothrombin time (PT), or activated partial thromboplastin time (aPTT).
- Presence of clinically relevant electrocardiogram (ECG) abnormalities prior to dosing such as QT interval corrected for heart rate using Fredericia's formula (QTcF) > 460 ms, personal or family history of congenital long QT syndrome indicating safety risk in the Investigator's opinion. First-degree atrioventricular block or isolated right bundle branch block is allowed.
- Clinically relevant disease or condition, including hematological, hepatic, cardiac or renal disease or abnormality, that would, in the judgement of the Investigator, pose an unacceptable risk to the participant or interfere with the conduct of the study
- Any concomitant condition that might interfere with the clinical evaluation of AS and that is not related to AS.
- Known history of human immunodeficiency virus (HIV), hepatitis B, C, or E virus.
- Any condition that increases the risk of meningitis.
- History of bleeding diathesis or coagulopathy.
Medical history of brain or spinal disease that would interfere with the LP process, CSF circulation or safety assessment, including:
- Tumors or abnormalities detected by magnetic resonance imaging (MRI) or computed tomography (CT),
- Subarachnoid hemorrhage,
- Clinical suggestion of raised intracranial pressure confirmed by MRI or ophthalmic examination,
- Spinal stenosis or curvature (considered sufficient to prohibit LP),
- Chiari malformation,
- Hydrocephalus,
- Syringomyelia,
- Tethered spinal cord syndrome and connective tissue disorders such as Ehlers-Danos syndrome and Marfan syndrome,
- Radiculopathy or radiculitis.
- Ventriculoperitoneal (VP) shunt for the drainage of CSF or an implanted CNS catheter.
- Medical history of brain or spinal injury, of traumatic, hemorrhagic, or any other origin, that may result in symptoms interfering with AS.
- History of clinically significant post LP headache of moderate or severe intensity and/or blood patch that would, in the judgement of the Investigator, pose an unacceptable risk to the participant or interfere with the conduct of the study.
- Malignancy within 5 years of screening.
- Hospitalization for any major medical or surgical procedure involving general anesthesia planned during the study, or within 4 weeks prior to screening, that - in the opinion of the Investigator - may pose a risk to the participant.
- Prohibited use of antiplatelet or anticoagulant therapy for 2 weeks prior to screening and at the time of enrolment.
- Have any other conditions which would make the participant unsuitable for inclusion or could interfere with the participant participating in or completing the study, including any contraindication to administration of IT therapy.
- Extremely or very preterm birth complications which, in the opinion of the Investigator, may interfere with study outcomes.
- Birth complications, confirmed or suspected asphyxia before, during, or after birth.
- Ascertained or presumptive hypersensitivity to the investigational medicinal product (IMP) or its excipients.
- Participated in a clinical trial and received an IMP within 90 days or 5 half-lives (whichever is longer) or tested an investigational medical device within 90 days prior to dosing or if the device is still active.
- Concurrent or planned concurrent participation in any clinical study (including observational, non-drug and non-interventional studies) without a signed data sharing agreement in place between the other clinical study and the Sponsor.
- Previous participation in cellular therapy, gene therapy, gene editing, or any other gene expression modulating clinical trial, such as an ASO treatment.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Cuadruplicar
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador falso: Impostor
Procedimiento simulado
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Sham Procedure
|
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Experimental: rugonersen
Study Drug
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Study Drug
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change from baseline in the Bayley-4 cognition and/or expressive communication raw scores without caregiver input at Week 56.
Periodo de tiempo: Baseline to week 56
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The Bayley-4 is a performance-based assessment of developmental functioning of five core battery scales: cognitive, language (two subtests: expressive and receptive communication), motor (two subtests: gross and fine motor), social-emotional, and adaptive behavior.
Change from baseline in the raw scores of the cognition and/or expressive communication scales of the Bayley-4, without caregiver input, higher change reflects a better outcome of the core scales.
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Baseline to week 56
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change from baseline in electroencephalogram (EEG) delta-band power at Week 56.
Periodo de tiempo: Week 56
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Change from baseline in electroencephalogram (EEG) delta-band power at Week 56.
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Week 56
|
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Incidence of serious adverse events (SAEs).
Periodo de tiempo: Week 60
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Incidence of serious adverse events (SAEs).
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Week 60
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Symptoms of Angelman Syndrome - Clinician Global Impression of Change (SAS-CGI-C) overall at Week 56.
Periodo de tiempo: Week 56
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The SAS-CGI-C is a Symptoms of Angelman Syndrome - Clinician Global Impression of Change that has been developed for Angelman Syndrome.
The SAS-CGI-C is a nine domain, clinician-rated measure, which assesses the clinician's impression of the severity of a participant's condition ranging from "very much improved" (1) to "very much worse" (7).
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Week 56
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Director de estudio: Brenda Vincenzi, MD, OHB Pediatrics Ltd.
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 (Actual)
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
Términos MeSH relevantes adicionales
- Trastornos de impronta
- Enfermedades del Sistema Nervioso Central
- Enfermedades del Sistema Nervioso
- Enfermedades Genéticas Congénitas
- Anomalías congénitas
- Trastornos del movimiento
- Anomalías Múltiples
- Trastornos cromosómicos
- Enfermedades y anomalías congénitas, hereditarias y neonatales
- Síndrome de Angelman
Otros números de identificación del estudio
- OHB-724-301
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. .