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

The HALOS study is investigating a new medication called ION582 for people with Angelman syndrome. The main goals are to check if the medicine is safe at different doses and how well people tolerate it. Researchers also want to understand how the medicine works in the body and its effects on Angelman syndrome. This study is split into several parts and will involve around 70 participants, ranging from babies to adults up to 50 years old. A recent change means that younger children (under 2 years old) with Angelman syndrome can now join at some locations. If you're interested, it's best to speak with your doctor or the study team for more details.

Auf einen Blick

Status
Aktiv, aber nicht rekrutierend
Phase
PHASE1, PHASE2
Sponsor
Ionis Pharmaceuticals, Inc.
Einschreibeziel
71
Starten
22 Dec 2021
Geschätzte Fertigstellung
01 Mar 2029

Worum geht es in dieser Studie?

The HALOS study is a clinical trial focused on a new experimental medicine called ION582, designed for individuals with Angelman syndrome. Angelman syndrome is a complex genetic condition that affects development, often causing learning difficulties, problems with speech, movement, and sometimes seizures. There is currently no cure, so new treatments are really important.

This study has several aims. First, it wants to find out if ION582 is safe to use at different dose levels. This is always the first step for any new medicine. Secondly, researchers will be looking at how the body processes the medicine – how it's absorbed, distributed, and eventually leaves the body. Finally, they want to understand if ION582 has any positive effects on the symptoms of Angelman syndrome.

This is a 'Phase 1-2a' study, meaning it's an early-stage study focusing on safety, but also looking for the first signs that the treatment might work. It's an 'open-label' study, which means both the participants and the medical team will know who is receiving the study medicine. The study will happen in different stages, with some participants potentially being in the study for several years to see the long-term effects of the medicine.

Wichtige Erkenntnisse

  • This study is testing a new medicine, ION582, for Angelman syndrome.
  • It aims to check the safety and how well people tolerate different doses.
  • Participants can range from babies to adults up to 50 years old.
  • The medicine is given through injections into the spinal fluid.
  • Participation could involve regular hospital visits over several years.
  • A recent update allows some sites to recruit children under 2 years old.

Wer könnte berechtigt sein?

To be considered for this study, individuals must have a confirmed diagnosis of Angelman syndrome due to a specific gene change (called a 'UBE3A deletion' or 'UBE3A mutation'). The study is open to both males and females between birth and 50 years of age. For those under 18, a parent or legal guardian would need to agree to their participation.

It's important that any other treatments for Angelman syndrome, such as seizure medications, sleep aids, or special diets, have been stable for at least three months before joining. This helps the researchers understand the effects of the new study medicine more clearly. One unique request is that participants (or their guardians) agree not to share personal or study information on social media until the study is officially finished.

However, some people would not be able to take part. This includes those whose Angelman syndrome is caused by a different genetic change (called 'paternal uniparental disomy' or 'imprinting defect'). Also, if someone has other serious medical conditions that the doctor thinks would make taking part unsafe, or if they have poorly controlled seizures, they would not be eligible. People who have certain bone or bleeding problems, or have had gene therapy in the past, also cannot join. If you've been vaccinated against COVID-19, that's absolutely fine, you can still participate.

Könnte diese Studie für Sie geeignet sein?

Beantworten Sie diese kurzen Fragen, um zu sehen, ob Sie möglicherweise berechtigt sind. Dies ist nur ein Leitfaden – das Forschungsteam trifft die endgültige Entscheidung.

  1. Do you (or the person you care for) have a confirmed Angelman syndrome diagnosis due to a UBE3A deletion or mutation?
  2. Are you (or the person you care for) between birth and 50 years old?
  3. Have any other Angelman syndrome treatments been stable for at least 3 months?
  4. Are there any other serious health conditions that might make participating unsafe?
  5. Have you (or the person you care for) had gene therapy in the past?
  6. Are you able to commit to not sharing study information on social media until complete?
Beantworten Sie jede Frage, um Ihr Ergebnis zu sehen.

Was beinhaltet die Teilnahme?

If you join the HALOS study, you would first go through a screening period to check if you meet all the requirements. The study medicine, ION582, is given directly into the fluid around the spinal cord (this is called an 'intrathecal' injection). This is similar to how some pain medications are given.

The study is divided into several parts. Part 1 involves receiving increasing doses of the medicine over 13 weeks, followed by at least 12 weeks of monitoring. If you complete Part 1, you might then move to Part 2, which involves receiving the medicine for 49 weeks, again followed by a monitoring period. For those who complete Part 2, there’s an option to continue receiving the medicine for up to another three years, followed by a final monitoring period. This means participating could involve regular hospital visits over several years, with check-ups, assessments, and the medicine being given. The full duration of the study for an individual could extend for several years.

Potenzielle Risiken und Vorteile

Taking part in a study like this comes with potential benefits and risks. A potential benefit could be that ION582 might help improve some of the symptoms of Angelman syndrome, though this is not guaranteed for anyone, and it is still very early in its development. The information gained from this study could also help countless others with Angelman syndrome in the future. However, there are risks associated with the study medicine itself, such as potential side effects, and risks from the procedures, like the spinal injections. The research team will explain all known risks to you in detail. It’s important to remember that participating is completely voluntary, and you have the right to withdraw from the study at any time, for any reason, without it affecting your medical care.

Standorte (11)

  • Rady Children's Hospital
    Verifizierte Postleitzahl
    San Diego, Vereinigte Staaten
  • Colorado Children's Hospital Research Institute
    Verifizierte Postleitzahl
    Aurora, Vereinigte Staaten
  • Rush Universitätsklinikum
    Verifizierte Postleitzahl
    Chicago, Vereinigte Staaten
  • Boston Kinderkrankenhaus
    Verifizierte Postleitzahl
    Boston, Vereinigte Staaten
  • University of North Carolina at Chapel Hill School of Medicine
    Verifizierte Postleitzahl
    Carrboro, United States
  • Texas Children's Hospital
    Verifizierte Postleitzahl
    Houston, Vereinigte Staaten
  • Sydney Children's Hospital, Kids Cancer Centre
    Verifizierte Postleitzahl
    Randwick, Australia
  • Necker-Enfants Malades Hospital
    Verifizierte Postleitzahl
    Paris, Frankreich
  • Sheba Medizinisches Zentrum
    Verifizierte Postleitzahl
    Ramat Gan, Israel
  • Azienda Ospedaliera Universitaria Pisana
    Verifizierte Postleitzahl
    Pisa, Italien
  • STRONG Group University of Oxford
    Verifizierte Postleitzahl
    Oxford, Vereinigtes Königreich

Häufige Fragen

What is Angelman syndrome?

Angelman syndrome is a genetic condition affecting development, causing learning difficulties, speech and movement problems, and sometimes seizures.

What is ION582?

ION582 is an experimental medicine being tested in this study to see if it can help people with Angelman syndrome.

Wie wird das Medikament verabreicht?

The medicine is given directly into the fluid around the spinal cord through an injection, similar to some pain procedures.

Can young children join the study?

Yes, a recent change means that children under 2 years old with Angelman syndrome can now join at some study locations.

What is the study called?

The study is called HALOS.

Wie Sie mehr erfahren können

Sprechen Sie immer mit Ihrem Hausarzt oder Spezialisten, bevor Sie sich entscheiden, an einer Studie teilzunehmen.

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