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RecruitingPHASE1INTERVENTIONAL

A Study of SGT-501 Gene Therapy in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)

This study is looking at a new gene therapy, SGT-501, for people with a heart condition called Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT). CPVT can cause dangerous fast heartbeats. This is a very early study (Phase 1) to see if SGT-501 is safe and tolerable for people. Researchers will also be trying to find the right amount (dose) of the treatment to give. The study will start with adults (18 years and older). If things go well, younger people aged 7 to under 18 might be included later. Everyone in the study will get a single dose of SGT-501 and will be carefully monitored by doctors for five years to check their health.

At a glance

Status
Recruiting
Phase
PHASE1
Sponsor
Solid Biosciences Inc.
Enrolment target
18
Start
23 Feb 2026
Estimated completion
01 May 2031

What is this study about?

This research is looking into a new treatment called SGT-501 for a specific heart condition known as Catecholaminergic Polymorphic Ventricular Tachycardia, or CPVT. CPVT is a rare condition that can cause your heart to beat very fast and irregularly, especially during exercise or stress. These fast heartbeats can be dangerous.

The SGT-501 treatment is a type of gene therapy. This means it aims to correct the underlying genetic problem that causes CPVT. This is a very early stage of research, called a Phase 1 study. Its main goal is to find out if the treatment is safe for people and what the best amount (dose) to give is. It's the first time SGT-501 is being tested in humans, so safety is the top priority.

Initially, the study will involve adults aged 18 and over. If the results show that it is safe, doctors might then include young people aged between 7 and 18. Each person will receive one dose of SGT-501, and their health will be carefully watched for a total of five years to understand the long-term effects of the treatment.

Key takeaways

  • This is an early study of a new gene therapy for CPVT.
  • The main goal is to check the safety of the treatment (SGT-501) and find the right dose.
  • Initially, only adults with CPVT can join, with potential for younger participants later.
  • Participants will be closely monitored for five years after receiving a single treatment.
  • Taking part helps advance medical knowledge, but personal benefits are not guaranteed.

Who may be eligible?

To join this study, you must have a clear diagnosis of CPVT, meaning you've had dangerous fast heartbeats during exercise or similar problems. Your doctors will also need to confirm that your CPVT is caused by a specific genetic change (called a RYR2 variant).

It's important that you've had serious heart events in the past, such as a collapsed because of your heart, or required an electric shock from a device (ICD) to correct your heartbeat. You must also be on a stable dose of your current heart medication (like beta-blockers or flecainide) for at least a month.

There are also some health conditions that would prevent you from joining. For example, if you have certain liver or kidney problems, or issues with your blood clotting. You'll also need to be up-to-date with your meningitis vaccination or be willing to get it.

Could this study suit you?

Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.

  1. Do I have a confirmed diagnosis of CPVT?
  2. Have I had a serious heart event (like collapsing or needing an ICD shock)?
  3. Am I 18 years old or older (or between 7 and 18 if the study expands)?
  4. Am I currently on a stable dose of my CPVT medication?
  5. Do I have any serious problems with my liver, kidneys, or blood clotting?
  6. Am I up-to-date with my meningitis vaccination, or willing to get it?
Answer every question to see your result.

What does participation involve?

If you join this study, you would receive a single dose of the SGT-501 gene therapy given directly into your vein. Doctors will then carefully monitor your health for a long time. The first year is considered the active treatment period, where you'll have more regular check-ups. After that, monitoring will continue for another four years, totalling five years of follow-up care to see how you are doing in the long term. This will involve regular visits to the clinic for tests and examinations.

Potential risks and benefits

As this is a very early study, the main potential benefit is helping researchers understand if this new gene therapy could be a safe and effective treatment for CPVT in the future. However, there's no guarantee that you will personally benefit from taking part. Potential risks are not fully known yet, as it's the first time this treatment is being used in people. Possible side effects of gene therapy can include reactions to the treatment or effects on other organs. All participants have the right to leave the study at any time, without it affecting their usual medical care.

Locations (5)

  • Boston Children's Hospital
    Verified postcode
    Boston, United States· Recruiting
  • Mayo Clinic
    Verified postcode
    Rochester, United States· Recruiting
  • Cleveland Clinic
    Verified postcode
    Cleveland, United States· Recruiting
  • University of Pennsylvania
    Verified postcode
    Philadelphia, United States· Not yet recruiting
  • St. Paul's Hospital
    Verified postcode
    Vancouver, Canada· Recruiting

Common questions

What is CPVT?

CPVT is a rare heart condition that can cause dangerous, fast heartbeats, especially during exercise or stress.

What is SGT-501?

SGT-501 is a new type of gene therapy being tested to see if it can help correct the genetic problem that causes CPVT.

Who can take part in this study?

Initially, adults aged 18 and over with a clear diagnosis of CPVT and a history of serious heart events can join. Younger people might be included later.

How long will I be monitored?

You will be carefully watched by doctors for a total of five years after receiving the treatment.

Is this treatment guaranteed to work?

No, this is an early-stage study, and there's no guarantee the treatment will work. The main goal is to check its safety and find the right amount to give.

How to find out more

Solid Bio Clinical Trials

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

Interested in taking part?

Register your interest

Share your details and the research team for "A Study of SGT-501 Gene Therapy in Catecholaminergic Polymor…" will contact you if you may be eligible. Always speak to your GP before agreeing to take part.

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