Remibrutinib for Multiple Sclerosis

(RemiSeven Trial)

SP
Overseen BySarah Planchon, MS, PhD
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a medication called remibrutinib to evaluate its effectiveness for people with multiple sclerosis (MS), a condition where the immune system mistakenly attacks the protective covering of nerves. Researchers aim to assess the safety and effectiveness of this treatment, as well as its impact on the brain, using MRI scans. Individuals with relapsing or progressive forms of MS who have experienced disease activity or worsening symptoms in the past year might be suitable candidates. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to important early findings.

Do I have to stop taking my current medications for the trial?

Yes, you will need to stop taking any disease-modifying therapy for MS or systemic immunotherapy for other autoimmune disorders to participate in this trial. Other medications may be reviewed on a case-by-case basis.

Is there any evidence suggesting that remibrutinib is likely to be safe for humans?

Research has shown that remibrutinib is generally safe. In various studies, participants tolerated remibrutinib well, even at a dose of 100 mg taken twice daily. A combined safety review confirmed this, demonstrating consistent safety across different uses and doses. These findings suggest that remibrutinib is usually safe for individuals with immune-related diseases, such as multiple sclerosis. While any medication can carry risks, current data supports the safety of remibrutinib for further study and potential use.12345

Why do researchers think this study treatment might be promising for MS?

Unlike the standard treatments for multiple sclerosis, which often include medications like interferons or monoclonal antibodies, Remibrutinib works by targeting Bruton's tyrosine kinase (BTK), a different mechanism of action. This is significant because BTK plays a crucial role in the activation of immune cells that are involved in the inflammation and nerve damage seen in multiple sclerosis. Researchers are excited about Remibrutinib because this targeted approach may offer a more precise way to manage the disease, potentially leading to fewer side effects and improved outcomes for patients. Additionally, Remibrutinib is administered orally, which could be more convenient compared to some existing treatments that require injections or infusions.

What evidence suggests that remibrutinib might be an effective treatment for multiple sclerosis?

Research has shown that remibrutinib, which participants in this trial will receive, may help treat multiple sclerosis (MS). Studies have found that remibrutinib works well compared to teriflunomide, a common MS treatment, potentially reducing relapses in people with relapsing forms of MS. Additionally, researchers have detected remibrutinib in the fluid around the brain and spine, indicating it can reach the brain where needed. These findings provide strong evidence for its potential to manage MS symptoms.16789

Who Is on the Research Team?

MA

Moein Amin, MD, MS

Principal Investigator

The Cleveland Clinic

Are You a Good Fit for This Trial?

Adults aged 18-60 with relapsing or progressive Multiple Sclerosis (MS) can join. They must have an MS diagnosis confirmed by McDonald Criteria, an EDSS score of 0-6.5, and recent disease activity or worsening disability. Participants need good vision, motor function, and stable health for the past month. Women must use double contraception if not postmenopausal or sterilized; men should also use contraception unless they've had a vasectomy.

Inclusion Criteria

I am between 18 and 60 years old.
My MS diagnosis is confirmed and follows the 2024 McDonald Criteria.
My disability level allows me to walk at least a little without help.
See 7 more

Exclusion Criteria

Ongoing substance abuse or any other factor that may interfere with the participant's ability to cooperate and comply with study procedures
Pregnancy, planned or current
Hematological abnormalities at screening
See 20 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive 100 mg remibrutinib twice daily with periodic MRIs, blood tests, EKGs, and physical exams to assess safety, tolerability, and efficacy

24 months
4 MRIs, periodic blood tests, EKGs, and physical exams

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Remibrutinib
Trial Overview The trial is testing Remibrutinib taken twice daily over two years in about 20 people with MS. It's focused on changes seen in MRI scans as the main goal, while also checking how safe and effective the drug is compared to what we already know about treating MS.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Remibrutinib, active administrationExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Moein Amin

Lead Sponsor

Novartis Pharmaceuticals

Industry Sponsor

Trials
2,963
Recruited
4,275,000+
Founded
1996
Headquarters
Basel, Switzerland
Known For
Precision medicine
Top Products
Gleevec, Cosentyx, Entresto, Kisqali
Dr. Vas Narasimhan profile image

Dr. Vas Narasimhan

Novartis Pharmaceuticals

Chief Executive Officer since 2018

MD from Harvard Medical School

Dr. Shreeram Aradhye profile image

Dr. Shreeram Aradhye

Novartis Pharmaceuticals

Chief Medical Officer since 2021

MD

Citations

NCT06846281 | Efficacy and Safety of Remibrutinib After ...The study is a randomized, open-label, non-inferiority multi-center, Phase 3b study to provide efficacy, safety, and tolerability data for remibrutinib ...
Efficacy and Safety of Remibrutinib Compared to ...To compare the efficacy and safety of remibrutinib versus teriflunomide in patients with relapsing multiple sclerosis (RMS)
Phase 3 REMODEL I/II Trials: Efficacy, Safety, and ...The REMODEL I and II studies will investigate the efficacy, safety, and tolerability of remibrutinib versus teriflunomide to support regulatory approval ...
A review of Bruton's tyrosine kinase inhibitors in multiple ...Remibrutinib has shown high efficacy in the treatment of CSU in a phase IIb study. Daily dosages of up to 600 mg were investigated in phase I, ...
Remibrutinib Exposure in Cerebrospinal Fluid: Insights ...Remibrutinib was successfully measured in the CSF of all participants in the remibrutinib group at all timepoints, whereas it was not detected ...
Efficacy and Safety of Remibrutinib After Switching From ...The purpose of this Phase 3b study is to assess the efficacy, safety and tolerability of remibrutinib after switching from ocrelizumab and compared to ...
Safety of Remibrutinib Across Immune-mediated Diseases ...This integrated safety analysis confirmed the consistently favorable safety profile of remibrutinib across indications and doses, including 100 mg twice daily.
156. Safety of Remibrutinib across Immune-mediated ...This integrated safety analysis confirmed the consistently favorable safety profile of remibrutinib across indications and doses, including 100 mg twice daily.
Efficacy, Safety, and Tolerability of Remibrutinib in Patients ...Remibrutinib is a potent, highly selective, covalent BTK inhibitor with a promising pharmacological and safety profile. Material(s) and Method(s). REMODEL I and ...
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