- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07825402
A Trial of ONO-2808 in Participants With the Parkinsonian Subtype of Multiple System Atrophy (MSA-P)
A Phase 3, Randomized, Double-blind, Placebo-controlled Study of ONO-2808 in Participants With the Parkinsonian Subtype of Multiple System Atrophy (MSA-P)
The main goal of this clinical trial is to learn if ONO-2808 works to treat adults with the Parkinsonian subtype of Multiple System Atrophy (MSA-P). Researchers will compare ONO-2808 to a placebo (a look-alike substance that contains no drug) to see if ONO-2808 works to treat MSA-P.
Participants will:
- Take ONO-2808 or placebo orally for up to 48 weeks
- Make visits to the clinic for checkups and tests
- Answer questions about their health throughout the trial.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Clinical Team
- Número de teléfono: 888-724-3274
- Correo electrónico: clinicaltrials@deciphera.com
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Key Inclusion Criteria:
- Participants with a diagnosis of clinically established or clinically probable MSA-P according to the 2022 Movement Disorder Society (MDS) criteria for MSA diagnosis.
Participants in the early stages of the disease, defined as a maximum of 5 years since the onset of one of the following symptoms associated with MSA-P:
- Parkinsonism
- Orthostatic hypotension
- Urinary dysautonomia
- Participants with an anticipated survival of at least 3 years in the opinion of the Investigator.
- Participants who are able to ambulate without the assistance of another person, defined as the ability to take at least 10 steps and then to turn around and walk at least another 10 steps. Use of assistive devices (eg, walker or cane) is allowed.
- Ability to swallow oral medication and willingness to adhere to the study drug regimen.
- Normal range of laboratory values at screening and baseline, especially liver function tests.
- Participants receiving treatment (including chronic medications, and herbal or dietary supplements) for symptoms associated with MSA must be on a stable dosage for at least 60 days prior to randomization based on the judgment of the Investigator. Participants must not initiate new treatment within 60 days prior to randomization.
Key Exclusion Criteria:
- Participants with the cerebellar subtype of MSA according to the 2022 MDS criteria for MSA diagnosis.
- Female participants who are pregnant, planning to become pregnant during the study, or breastfeeding.
- Participants with a clinically significant or unstable medical or surgical condition other than MSA-P that, in the opinion of the Investigator, might preclude safe completion of the study or might affect the results of the study (eg, pulmonary, cardiovascular [including bradyarrhythmia], macular edema, and significant renal or hepatic dysfunction).
- Neurological diseases/disorders other than MSA-P, such as Parkinson's disease, dementia with Lewy bodies, essential tremor, progressive supranuclear palsy, spinocerebellar ataxia, spastic paraparesis, corticobasal degeneration, or vascular, normal pressure hydrocephalus, pharmacological, or postencephalitic parkinsonism.
- Any abnormalities, other than MSA, found on the centrally read brain MRI that, in the opinion of the Investigator, may constitute a confounder for the study or preclude safe participation.
- Participants with documented liver diseases, cirrhosis, prior drug-induced liver injury (DILI), or ascites or symptoms and signs of encephalopathy due to hepatic dysfunction.
Other protocol-defined inclusion and exclusion criteria apply.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador de placebos: Placebo
|
Matching placebo will be administered to participants orally once daily for 48 weeks.
|
|
Experimental: ONO-2808 Low Dose
|
ONO-2808 will be administered to participants orally once daily for 48 weeks.
|
|
Experimental: ONO-2808 High Dose
|
ONO-2808 will be administered to participants orally once daily for 48 weeks.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Change from Baseline in modified United Multiple System Atrophy Rating Scale (mUMSARS) Part I (excluding Item 11) with Collapsed Scoring (0-3)
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Change from Baseline in Multiple System Atrophy Quality of Life Scale (MSA-QoL) Motor Subscale Score
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Magnetic Resonance Imaging (MRI) Volumetric Assessments
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Total United Multiple System Atrophy Rating Scale (UMSARS) Score (Part I and Part II, all items)
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in mUMSARS Score
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in MSA-QoL Total Score
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Patient Global Impression of Change (PGI-C) Score
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Patient Global Impression of Severity (PGI-S) Score
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Clinical Global Impression of Change (CGI-C) Score
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Clinical Global Impression of Severity (CGI-S) Score
Periodo de tiempo: Baseline, Week 48
|
Baseline, Week 48
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Director de estudio: Clinical Team, Ono Pharmaceutical Co., Ltd.
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
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
Palabras clave
Términos MeSH relevantes adicionales
- Sinucleinopatías
- Enfermedades Cerebrales
- Enfermedades del Sistema Nervioso Central
- Enfermedades del Sistema Nervioso
- Enfermedades neurodegenerativas
- Enfermedades de los ganglios basales
- Disautonomías primarias
- Enfermedades del sistema nervioso autónomo
- Trastornos del movimiento
- Enfermedad de Parkinson
- Atrofia multisistémica
- Trastornos Parkinsonianos
Otros números de identificación del estudio
- ONO-2808-03-001
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. .