- ICH GCP
- Registr klinických studií v USA
- Klinická studie 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
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Detailní popis
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 3
Rozšířený přístup
Kontakty a umístění
Studijní kontakt
- Jméno: Brenda Vincenzi, MD
- Telefonní číslo: +18573022294
- E-mail: patientadvocacy@oakhillbio.com
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dítě
- Dospělý
Přijímá zdravé dobrovolníky
Popis
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.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Čtyřnásobek
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Falešný srovnávač: Falešný
Předstíraný postup
|
Sham Procedure
|
|
Experimentální: rugonersen
Study Drug
|
Study Drug
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Change from baseline in the Bayley-4 cognition and/or expressive communication raw scores without caregiver input at Week 56.
Časové okno: Baseline to week 56
|
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.
|
Baseline to week 56
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Change from baseline in electroencephalogram (EEG) delta-band power at Week 56.
Časové okno: Week 56
|
Change from baseline in electroencephalogram (EEG) delta-band power at Week 56.
|
Week 56
|
|
Incidence of serious adverse events (SAEs).
Časové okno: Week 60
|
Incidence of serious adverse events (SAEs).
|
Week 60
|
|
Symptoms of Angelman Syndrome - Clinician Global Impression of Change (SAS-CGI-C) overall at Week 56.
Časové okno: Week 56
|
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).
|
Week 56
|
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Vyšetřovatelé
- Ředitel studie: Brenda Vincenzi, MD, OHB Pediatrics Ltd.
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
Další identifikační čísla studie
- OHB-724-301
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
Klinické studie na Angelmanův syndrom
-
GlaxoSmithKlineZatím nenabíráme
-
Charite University, Berlin, GermanyNáborSyndrom postintenzivní péčeNěmecko
-
Unravel Biosciences, Inc.NáborPitt Hopkinsův syndromKolumbie
-
Lokman Hekim UniversityDokončenoSubakromiální impingement syndrom | Syndrom nárazového ramene | Syndrom nárazu rotátorové manžetyTurecko (Türkiye)
-
Cairo UniversityDokončeno
-
Cairo UniversityDokončeno
-
Ministry of Public Health, Democratic Republic...National Institutes of Health (NIH); Oregon Health and Science University; National... a další spolupracovníciDokončenoSyndrom neurotoxicity, Cassava | Syndrom neurotoxicity, kyanát | Syndrom neurotoxicity, kyanid | Syndrom neurotoxicity, thiokyanátKongo, Demokratická republika
-
Cliniques universitaires Saint-Luc- Université...UkončenoSyndrom multiorgánové dysfunkce | SEPTICKÝ ŠOK | SYNDROM SEPSEBelgie
-
Neuren Pharmaceuticals LimitedNáborPhelan-McDermidův syndromSpojené státy
-
University of California, Los AngelesBoston Children's Hospital; Duke University; Children's Hospital Medical Center...NáborBohring-Opitzův syndrom | Genová mutace ASXL1 | Syndrom Shashi-Pena | Genová mutace ASXL2 | Bainbridge-Ropersův syndrom | Genová mutace ASXL3Spojené státy