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RecruitingPHASE3INTERVENTIONAL

A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult and Adolescent Patients With Moderate to Severe Hidradenitis Suppurativa

This research study is looking into a new medicine called remibrutinib for people aged 12 and older who have moderate to severe hidradenitis suppurativa (HS). HS is a long-term skin condition that causes painful lumps and boils. The study aims to find out if remibrutinib works well, if it's safe to use, and how well people tolerate it compared to a placebo (a dummy pill with no active medicine). Participants will receive one of two doses of remibrutinib or a placebo. The study will last about 76 weeks, including screening, treatment periods, and a follow-up to check on participants' health after stopping the medication.

At a glance

Status
Recruiting
Phase
PHASE3
Sponsor
Novartis Pharmaceuticals
Enrolment target
555
Start
20 Mar 2025
Estimated completion
07 Feb 2028

What is this study about?

This study is particularly important for people living with hidradenitis suppurativa, often called HS. HS is a challenging skin condition that causes painful, inflamed lumps under the skin, often in areas like the armpits or groin. These lumps can sometimes break open and release pus, leading to scarring. Finding new and better ways to manage HS is crucial because current treatments don't work for everyone or can have side effects.

The main goal of this research is to see if a new medicine, remibrutinib, can help reduce the symptoms of moderate to severe HS and improve quality of life. The study will carefully compare remibrutinib to a placebo, which looks like the active medicine but has no drug in it. This comparison helps researchers understand if any improvements seen are truly due to the medicine or if they might happen anyway.

By taking part, you could contribute to developing new treatment options for HS. Every participant's experience, whether they receive the active medicine or the placebo, provides valuable information that helps medical science advance. This type of study is a vital step in making new medicines available to patients in the future.

Key takeaways

  • This study is testing a new medicine, remibrutinib, for moderate to severe hidradenitis suppurativa (HS) in people aged 12 and over.
  • It aims to check how well the medicine works, its safety, and if people can tolerate it.
  • Participants will receive either remibrutinib (two different doses) or a placebo (dummy pill) for most of the study.
  • The total study duration is approximately 76 weeks, with regular clinic visits.
  • Strict rules apply for who can and cannot join, based on age, HS severity, and other health conditions.
  • You can stop participating at any time if you change your mind.

Who may be eligible?

To join this study, you must be at least 12 years old. You need to have been diagnosed with hidradenitis suppurativa (HS) for at least 6 months and have a moderate to severe form of the condition. This means you should have at least 5 active lumps (abscesses or inflamed nodules) and these should affect at least two different areas of your body, for example, both armpits.

There are also some reasons why you might not be able to join. For example, if you have more than 20 tunnels or channels (fistulas) on your skin, or if you have other serious skin conditions that would make it hard to assess your HS. You also can't have taken remibrutinib or similar medicines before. If you're currently taking other experimental drugs or certain blood thinners, that might also make you ineligible.

The study also can't accept you if you have certain medical conditions like severe liver problems, a high risk of bleeding, specific heart, kidney, or lung conditions, or known allergies to any of the study drug ingredients. Your study doctor will review all your health information carefully to make sure the study is safe for you.

Quick self-check
  • Are you 12 years old or older?
  • Have you been diagnosed with HS for at least 6 months?
  • Do you have at least 5 active HS lumps (abscesses/nodules) affecting at least two different body areas?
  • Do you have less than 20 skin tunnels/fistulas?
  • Have you never taken remibrutinib or similar medicines before?
  • Do you have good overall health, without serious liver, bleeding, or other specific health problems mentioned?

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

What does participation involve?

If you decide to take part in this study, the total commitment will be about 76 weeks, or roughly a year and a half. This time includes several stages.

First, there's a screening period of up to 4 weeks, where doctors check if you're suitable for the study. After that, you'll enter Treatment Period 1, which lasts 16 weeks. During this time, you will be given either remibrutinib (one of two different doses) or a placebo (a dummy pill). Neither you nor your study doctor will know which one you are receiving – this is called 'double-blind'.

Following this, there's Treatment Period 2, lasting 52 weeks, where you will continue to receive remibrutinib. Throughout these treatment periods, you'll have regular visits to the clinic so the study team can monitor your health, check how your HS is reacting to the treatment, and manage any side effects. These visits will involve physical examinations, blood tests, and discussions about your symptoms.

Finally, after you stop taking the study medicine, there's a 4-week Safety Follow-Up period. This is to ensure you're doing well and to check for any lasting effects. You are encouraged to stay in the study even if you stop taking the treatment early, but if you don't want to, you would still complete this 4-week safety check.

Potential risks and benefits

Taking part in this study might offer potential benefits, such as receiving a new investigational treatment for your HS and having your health closely monitored by medical professionals. However, there's no guarantee that the study medicine will improve your condition, or you might receive the placebo. Potential risks could include side effects from the medication, which would be explained in detail by the study team. You always have the right to withdraw from the study at any time, for any reason, without it affecting your usual medical care.

Locations (138)

  • Total Skin and Beauty Dermatology Center PC
    Birmingham, United States· Recruiting
  • CTT Research
    Gilbert, United States· Recruiting
  • Ctr Dermatology and Plastic Surgery
    Scottsdale, United States· Recruiting
  • Ctr for Dermatology Clinical Res
    Fremont, United States· Recruiting
  • USC Keck School of Medicine
    Los Angeles, United States· Recruiting
  • MedDerm Associates
    San Diego, United States· Recruiting
  • Driven Research
    Coral Gables, United States· Recruiting
  • Floridian Research Institute
    Miami, United States· Recruiting
  • Sarasota Arthritis Res Ctr
    Sarasota, United States· Recruiting
  • University Of South Florida
    Tampa, United States· Recruiting
  • Emory School of Med Dermatology
    Atlanta, United States· Recruiting
  • Atlanta Biomedical Clin Res LLC
    Atlanta, United States· Recruiting

+126 more sites — see the official record for the full list.

Common questions

What is hidradenitis suppurativa (HS)?

HS is a long-term skin condition causing painful lumps and boils, often in body folds like armpits or groin.

What is remibrutinib?

Remibrutinib is a new medicine being tested to see if it can help people with moderate to severe HS.

What is a placebo?

A placebo is a 'dummy pill' that looks like the study medicine but doesn't contain any active drug. It helps researchers compare the real medicine's effects.

How long will the study last?

The study will last about 76 weeks in total, including screening, treatment, and follow-up periods.

Can I leave the study at any time?

Yes, you are free to leave the study at any point, and it will not affect your ongoing medical care.

How to find out more

Novartis Pharmaceuticals

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 Phase 3 Study to Assess Efficacy Safety and Tolerability o…" will contact you if you may be eligible. Always speak to your GP before agreeing to take part.

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