All studies
Active not recruitingPHASE3INTERVENTIONAL

FUSION: A Study to Evaluate the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of ION363 in Amyotrophic Lateral Sclerosis Participants With Fused in Sarcoma Mutations (FUS-ALS)

The FUSION study is exploring a new treatment, ION363, for a specific form of Motor Neurone Disease (MND) linked to a gene change called FUS-ALS. Researchers want to understand if ION363 can improve daily function and lengthen life for people with this condition. Participants will receive either ION363 or a dummy drug (placebo) for over a year, with the option to continue on ION363 afterwards. This study is in its final phase of testing before it might become widely available. Doctors and scientists are carefully looking into both how well the treatment works and if it is safe for those taking part.

At a glance

Status
Active not recruiting
Phase
PHASE3
Sponsor
Ionis Pharmaceuticals, Inc.
Enrolment target
89
Start
14 Jun 2021
Estimated completion
01 Mar 2028

What is this study about?

This study, called FUSION, is focused on a type of Motor Neurone Disease (MND) that is caused by a specific change in a gene known as FUS. This particular form of MND is called FUS-ALS. The main goal of this research is to see how effective a new medicine, called ION363, is at improving how people can do their daily activities and how long they live when they have FUS-ALS.

The study will involve up to 95 people and is split into three main parts. In the first part, some participants will receive the new medicine ION363, while others will get a placebo (a dummy drug with no active ingredients). This helps the researchers compare the effects of the real medicine. After about 14 months, everyone will have the chance to receive ION363 in an "open-label" way, meaning both they and their doctors will know they are getting the active drug.

This is a Phase 3 study, which means it's one of the last steps in testing a new medicine before it can be approved for wider use. The information gathered will be crucial for understanding if ION363 can make a real difference for people living with FUS-ALS.

Key takeaways

  • The study explores a new medicine (ION363) for FUS-ALS, a specific type of MND.
  • It aims to see if ION363 can improve daily function and extend life.
  • Participants will initially receive either ION363 or a placebo, then potentially ION363 for longer.
  • This is a late-stage study (Phase 3) before potential wider availability.
  • Eligibility includes having the FUS gene change and specific health/breathing requirements.
  • Participation involves regular clinic visits for assessments over potentially several years.

Who may be eligible?

To join the first part of this study, you need to be at least 10 years old and have symptoms of Motor Neurone Disease (MND) that a doctor believes are consistent with the condition. Crucially, you must have a confirmed change in your FUS gene, which will have been checked by a certified laboratory.

Your breathing capacity is also a factor. If your lung function (measured by something called 'slow vital capacity') is at least 50% of what's expected for someone of your age, sex, and height, you might be eligible. If it's less than 50%, you'd need to be between 10 and 30 years old, and your MND symptoms must have started within the last 12 months. Any current MND medicines you're taking, like riluzole or edaravone, must have been at a steady dose for at least 28 days before the study begins, and you'll need to agree to continue them at that dose throughout the study, unless your doctor decides otherwise.

All participants must also have stable other medications and nutritional support for at least a month before the study starts. For women, you cannot be pregnant or breastfeeding. Both men and women must agree to use specific contraception methods if needed, or be surgically sterile, or for women, past menopause. Finally, you’ll need a close friend or family member who can provide information about your abilities, as judged by the study doctor.

Quick self-check
  • Are you at least 10 years old?
  • Has a doctor said your symptoms are consistent with MND?
  • Do you have a confirmed FUS gene change?
  • Is your breathing capacity (SVC) at least 50% of expected, or if younger (10-30), did your symptoms start in the last year?
  • Are any existing MND medicines you take at a stable dose?
  • Are you able to attend regular study visits and have a caregiver who can provide information?

This is a guide only — the research team will confirm whether you can take part.

What does participation involve?

If you join the FUSION study, your involvement will be split into three stages. For the first stage, lasting about 60 weeks (just over a year), you will either receive ION363 or a placebo, chosen at random. This means there's a 2 in 3 chance you'll get ION363 and a 1 in 3 chance of getting the placebo. After this first stage, you'll have the option to continue into a second stage where everyone will receive ION363 for about 84 weeks (around 1.5 years). There's also a potential third stage where you could receive ION363 for up to three more years, or until the medicine becomes available generally, or the study programme ends.

Throughout the study, you'll have regular visits to the study clinic for assessments. These will include checking your general health, how your MND symptoms are progressing, and performing various tests to see how the medicine is affecting your body. The total time you could be in the study, if you participate in all three parts, could be several years.

Potential risks and benefits

Taking part in any medical study has potential benefits and risks. A potential benefit of this study is the chance to receive a new experimental medicine (ION363) that might help with FUS-ALS, especially if you are in the group receiving the active drug. However, there's no guarantee the medicine will help, and you might receive a placebo in the first part of the study. Possible risks could include side effects from the medication or discomfort from study procedures like blood tests. All potential risks will be thoroughly explained to you by the study team. It's important to remember that joining is always voluntary, and you have the right to leave the study at any time, for any reason, without it affecting your medical care.

Locations (25)

  • University of California San Diego
    La Jolla, United States
  • Stanford University Medical Center
    Palo Alto, United States
  • Johns Hopkins University
    Baltimore, United States
  • Massachusetts General Hospital
    Boston, United States
  • Washington University School of Medicine
    St Louis, United States
  • Columbia University Medical Center
    New York, United States
  • The Ohio State University Wexner Medical Center
    Columbus, United States
  • University of Utah
    Salt Lake City, United States
  • UZ Leuven
    Leuven, Belgium
  • PSEG Centro de Pesquisa Clinica S.A.
    São Paulo, Brazil
  • Montreal Neurological Institute
    Montreal, Canada
  • Universitaetsmedizin Rostock
    Rostock, Germany

+13 more sites — see the official record for the full list.

Common questions

What is FUS-ALS?

FUS-ALS is a specific type of Motor Neurone Disease (MND) that is caused by a change in a gene called FUS.

What is a placebo?

A placebo is a 'dummy' treatment that looks just like the real medicine but contains no active ingredients. It helps researchers compare the effects of the new drug.

How long will I be in the study?

The first part of the study lasts about 14 months, with options to continue on the active drug for several more years after that.

Can I continue my current MND medicines?

Yes, but they must have been at a steady dose for at least 28 days before the study starts, and you'll need to continue them at that dose unless your doctor advises otherwise.

Do I have to live near the study centre?

The study is taking place in multiple locations. You would need to be able to get to the study centre for regular visits.

How to find out more

Always speak to your GP or specialist before deciding to take part in a study.

Discussion

Community discussion

Powered by our forum at community.patient.info. Please be respectful — this is not medical advice.