HALOS: A Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of Multiple Ascending Doses of ION582 in Participants With Angelman Syndrome

Официальное название

HALOS: A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ION582 in Patients With Angelman Syndrome

Обзор

The purpose of this study is to evaluate the safety and tolerability of ascending doses of ION582 administered intrathecally in participants with Angelman syndrome.

Подробное описание

This is a Phase 1-2a, open-label study consisting of 3 parts in approximately 70 participants. Part 1 is a multiple ascending dose (MAD) study, consisting of a 13-week MAD Treatment Period and a minimum 12-week Post-MAD Follow-Up Period. Part 2 is a multi-center 49-week study where participants who completed Part 1 will receive IT bolus doses of ION582 followed by a minimum 12-week Part 2 follow up period. Part 3 extends the treatment period for participants who completed Part 2 for up to an additional 3 years followed by a 32-week post-LTE follow up period.

The study was amended in late 2025 to include a cohort of people with Angelman Syndrome under the age of 2 years old. Recruitment sites listed as "Recruiting" below are eligible to recruit individuals into this new cohort only. This page will continue to be updated to reflect the recruitment status of sites and the study. For more information, speak with your doctor or see the Study Contact information below.

Вмешательства

• Препарат ION582
  ION582 will be administered by IT injection.

Первичные конечные точки

• To evaluate the safety and tolerability of single and multiple doses of ION582 (incidence, severity, and dose-relationship of adverse effects and changes in the laboratory parameters). [Срок оценки: Part 1: Up to Week 45; Part 2: Up to Week 81]

Вторичные конечные точки (4)

• Maximum Observed Plasma Concentration (Cmax) of ION582 [Срок оценки: Part 1: Up to Week 45; Part 2: Up to Week 81]
• Time to Reach Maximal Plasma Concentration (Tmax) of ION582 [Срок оценки: Part 1: Up to Week 45; Part 2: Up to Week 81]
• Plasma Elimination Half-Life (t1/2λz) of ION582 [Срок оценки: Part 1: Up to Week 45; Part 2: Up to Week 81]
• Concentration ION582 in CSF [Срок оценки: Part 1: Up to Week 13; Part 2: Up to Week 49]

Критерии участия

Критерии включения

• Participant has a documented and certified diagnosis of Angelman syndrome (AS) (ubiquitin-protein ligase E3A \[UBE3A\] deletion or UBE3A mutation)
• Male or female between the ages of 0-50 years of age, with signed informed consent from parent(s) or legal guardian(s)
• Currently receiving stable standard of care treatments such as, stable doses of anti-epileptic medication, behavioral management medications, sleep medications, gabapentin, cannabidiol, and including special diets, supplements or nutritional support for at least 3 months prior to first dose.
• Follow good study practice and not participate in the sharing of personal or study information on social media platforms, such as any website or social media site (e.g., Facebook, Instagram, Twitter, YouTube, etc.) until notified that the study is completed.

Критерии исключения

• Has documented molecular AS confirmation of paternal uniparental disomy (UPD) or imprinting defect (ID).
• Any clinically significant (CS) cardiovascular, endocrine, hepatic, renal, pulmonary, gastrointestinal, neurologic, malignant, metabolic, psychiatric, or other condition that, in the judgment of the Investigator, will pose a safety risk, will make the patient unsuitable for participation in, and/or unable to complete the study procedures. Has poorly controlled seizures as determined by the Investigator or has documented Status Epilepticus in the past 6 months that could pose a safety risk while on study.
• Known bone, spine, bleeding, or other disorder that exposes the patient to risk of injury or unsuccessful lumbar puncture. Previous treatment with an oligonucleotide (including small interfering ribonucleic acid, antisense oligonucleotide \[ASOs\]). COVID-19 vaccinations are allowed.
• Any prior use of gene therapy. Have any other conditions, which, in the opinion of the Investigator would make the participant unsuitable for inclusion or could interfere with the participant taking part in or completing the study.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Нерандомизированное

Модель

Последовательный дизайн

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

США · 6 центров

• Rady Children's Hospital — San Diego
• Colorado Children's Hospital Research Institute — Aurora
• Rush University Medical Center — Chicago
• Boston Children's Hospital — Boston
• University of North Carolina at Chapel Hill School of Medicine — Carrboro
• Texas Children's Hospital — Houston

Австралия · 1 центр

• Sydney Children's Hospital, Kids Cancer Centre — Randwick

Франция · 1 центр

• Necker-Enfants Malades Hospital — Paris

Израиль · 1 центр

• Sheba Medical Center — Ramat Gan

Италия · 1 центр

• Azienda Ospedaliera Universitaria Pisana — Pisa

Великобритания · 1 центр

• STRONG Group University of Oxford — Oxford

Идентификаторы

NCT: NCT05127226 · ION582-CS1 · 2021-003009-23

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗