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- Registre américain des essais cliniques
- Essai clinique 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.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Clinical Team
- Numéro de téléphone: 888-724-3274
- E-mail: clinicaltrials@deciphera.com
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
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 d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur placebo: Placebo
|
Matching placebo will be administered to participants orally once daily for 48 weeks.
|
|
Expérimental: ONO-2808 Low Dose
|
ONO-2808 will be administered to participants orally once daily for 48 weeks.
|
|
Expérimental: ONO-2808 High Dose
|
ONO-2808 will be administered to participants orally once daily for 48 weeks.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Change from Baseline in modified United Multiple System Atrophy Rating Scale (mUMSARS) Part I (excluding Item 11) with Collapsed Scoring (0-3)
Délai: Baseline, Week 48
|
Baseline, Week 48
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Change from Baseline in Multiple System Atrophy Quality of Life Scale (MSA-QoL) Motor Subscale Score
Délai: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Magnetic Resonance Imaging (MRI) Volumetric Assessments
Délai: 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)
Délai: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in mUMSARS Score
Délai: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in MSA-QoL Total Score
Délai: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Patient Global Impression of Change (PGI-C) Score
Délai: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Patient Global Impression of Severity (PGI-S) Score
Délai: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Clinical Global Impression of Change (CGI-C) Score
Délai: Baseline, Week 48
|
Baseline, Week 48
|
|
Change from Baseline in Clinical Global Impression of Severity (CGI-S) Score
Délai: Baseline, Week 48
|
Baseline, Week 48
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Directeur d'études: Clinical Team, Ono Pharmaceutical Co., Ltd.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Synucleinopathies
- Maladies du cerveau
- Maladies du système nerveux central
- Maladies du système nerveux
- Maladies neurodégénératives
- Maladies des noyaux gris centraux
- Dysautonomies primaires
- Maladies du système nerveux autonome
- Troubles du mouvement
- Maladie de Parkinson
- Atrophie multisystématisée
- Troubles parkinsoniens
Autres numéros d'identification d'étude
- ONO-2808-03-001
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
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