Study on the Effectiveness and Safety of Frexalimab and Teriflunomide in Adults with Relapsing Multiple Sclerosis

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What is this study about?

This clinical trial is focused on studying the effectiveness and safety of a new treatment for multiple sclerosis, specifically for its relapsing forms. Multiple sclerosis is a condition where the immune system mistakenly attacks the protective covering of nerves, leading to communication problems between the brain and the rest of the body. The study will compare a new medication called frexalimab (also known by its code name SAR441344) with an existing treatment called teriflunomide, which is available as AUBAGIO 14 mg film-coated tablets. Frexalimab is administered as a solution for injection, while teriflunomide is taken orally in tablet form.

The purpose of the study is to assess how well frexalimab works compared to teriflunomide in reducing the frequency of relapses in people with relapsing forms of multiple sclerosis. Participants in the study will receive either frexalimab, teriflunomide, or a placebo, which is a substance with no active medication. The study will last for a period of up to 160 weeks, during which participants will be monitored for any changes in their condition, including the number of relapses they experience and any side effects they may encounter.

Throughout the study, various assessments will be conducted, such as MRI scans to detect changes in the brain, and tests to evaluate cognitive function and overall impact on daily life. The study will also monitor for any adverse events or reactions to the medications. The goal is to gather comprehensive data on the safety and effectiveness of frexalimab as a potential new treatment option for individuals with relapsing forms of multiple sclerosis.

1 initial visit

Upon joining the study, you will have an initial visit where your eligibility will be confirmed. This includes a review of your medical history and a physical examination.

You will be asked to provide information about any previous relapses or MRI scans showing specific brain changes related to multiple sclerosis.

2 randomization

After confirming eligibility, you will be randomly assigned to one of two groups. One group will receive the medication frexalimab, and the other will receive teriflunomide.

This process is random to ensure the study’s fairness and accuracy.

3 medication administration

If you are in the frexalimab group, you will receive this medication through an intravenous infusion, which means it will be given directly into your vein.

If you are in the teriflunomide group, you will take a 14 mg film-coated tablet orally once a day.

4 regular follow-up visits

You will have regular follow-up visits to monitor your health and the effects of the medication. These visits will include physical exams and possibly MRI scans to check for changes in your condition.

You will be asked about any side effects or changes in your symptoms.

5 end of study procedures

At the end of the study, you will have a final visit to assess your overall health and the impact of the treatment.

This may include a final physical exam, MRI scans, and discussions about your experience during the trial.

Who Can Join the Study?

  • The participant must have been diagnosed with relapsing multiple sclerosis (RMS) according to the 2017 revision of the McDonald diagnostic criteria. This means the participant has a specific type of multiple sclerosis that comes and goes.
  • The participant has an EDSS score of 5.5 or less at the first visit (Screening Visit). The EDSS score is a way to measure how much the disease affects the participant’s ability to move and perform daily activities.
  • The participant must have at least one of the following before the screening:
    • At least one documented relapse (a return of symptoms) within the previous year.
    • At least two documented relapses within the previous two years.
    • At least one documented Gd enhancing lesion on an MRI scan within the previous year. A Gd enhancing lesion is a specific type of change seen in the brain or spinal cord on an MRI scan, which indicates active inflammation.
  • Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. This means participants must follow local rules about birth control while in the study.
  • The study is open to both male and female participants.
  • The study includes participants who are considered part of a vulnerable population, meaning they may need extra protection or care.

Who Cannot Join the Study?

  • Patients who do not have a diagnosis of multiple sclerosis cannot participate.
  • Patients who are not within the specified age range for the study cannot participate.
  • Patients who are not willing or able to follow the study procedures cannot participate.
  • Patients who have other medical conditions that might interfere with the study cannot participate.
  • Patients who are pregnant or breastfeeding cannot participate.
  • Patients who are currently participating in another clinical trial cannot participate.
  • Patients who have had a recent infection or illness that could affect the study cannot participate.
  • Patients who have a history of drug or alcohol abuse cannot participate.
  • Patients who have allergies to the study medication or similar drugs cannot participate.
  • Patients who have received certain treatments or medications recently that could interfere with the study cannot participate.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
University Hospital Ostrava Ostrava Czechia
Hospital Da Luz S.A. Lisbon Portugal
Spitalul Universitar De Urgenta Bucuresti Bucharest Romania
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Nice Nice France
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital Del Mar Barcelona Spain
Clinexpert Kft. Budapest Hungary
Hospital Universitario De Cruces Barakaldo Spain
Hospital Universitari De Girona Doctor Josep Trueta Girona Spain
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
ARNAS Civico Di Cristina Benfratelli Palermo Italy
Resmedica Sp. z o.o. Kielce Poland
Ujwxqakhej Mrmjbefveflu Hjwseraf Fae Akfwpp Tpwjlcrob Aoy Eckvszfeq Mkkauaxm N I Pupyrmh Sofia Bulgaria
Gcaogwi Ubcmpxwtxf Hrzoyoqh Or Lkdomub Larissa Greece
Fvgbxxuu nypkmyrzo Mcgnc a Hejzhbk Prague Czechia
Vmidtdlt uhjauttsinwf lvcywipk Sjhoqqdu kxruedzy Vgb Vilnius Lithuania
Fiicpdxr Nabeemonh Bpag Brno Czechia
Pykgevfavtnpwillnucwd Mcmyhqo Marburg Germany
Hyflzibu Usgmrqvzgsxol Fudqrknsv Jkogtho Dobv Madrid Spain
Fwqliuhl Nbmouvhmh Kmfvgahdv Vzaviyalf Prague Czechia
Ihuay Odjpafpf Plkxgbgotvi Sws Mltrhsy Genoa Italy
Cmukoj Hxdxkmornc E Umpkihzylyqdo Dy Crcgxdl Ewwrzq Coimbra Portugal
Smdtvobreau Pdylajwfz Zraezr Ouqlei Zqbfhdddkk Squuubs Ugdkqjwsmorxg W Kkwwrndc Cracow Poland
Uuwmsucaijrfgrvxtuthy Meruuzmn Acu Munster Germany
Jumoetpv Krhyzh Uxpiwbwhbl Linz Austria
Jmxgbdbewpnzihxuqfaodrwhpn Gueeiwj Giessen Germany
Aqmjdaj Otncjevbkjcyglemmsfkyfmxq Molksqhy Dpdlh Cmsijf Novara Italy
Vxvfdspox Ftbkxwkh Naprmrfdh V Pzjos Prague Czechia
Rhodxrmcqfhruk Copenhagen Denmark
Uqkcqrtrutmfexpecpvbn Ejaxx Avs Essen Germany
Ukoxbbjkda Dfbym Stpvt Dk Rjio Ls Skrbhpgz Rome Italy
Aflqqjh Smqxxsjlv Urqdzuayifefp Fifwmj Cnsnyjsw Udine Italy
Umscucfquugqjrltb Doezw Sjsie Da Fhvhwea Ferrara Italy
Cspafnkk Hrtbpjqkpkua Ujahjsqiqdzzh Dj Vdcr Vigo Spain
Ubbmoqeacq Gylhtfb Hjxblscg Aglprjt Gqqxpwm Hsgujcfy Of Wwwn Axxtah H Ayqm Vqwwqcf Chaidari Greece
Cpnnzy Htbsnbwpzka Dp Ciyuqd Colmar France
Kwz Zbtwbu Zagreb Croatia
Appqhyb Olvjcynhfubcdrnqpauqhxgty Pahbpwujyzz Ge Rvbdwyahfwpw Mhsgq Dr Cxnapef Catania Italy
Mnzcfrxpqzqo Hmjjoisw Fpk Apgpzn Thohjscyg Iv Niebjwpog Ago Phzhgcwbce Sko Nfsa Eqv Sofia Bulgaria
Siarnasiw Kbpb Budapest Hungary
Chsxwf Hkmeuqerbzz Da Jgft Ezio Tsgkws Calais France
Nsyinimnqfyk Bffnlvoil Bielefeld Germany
Cgnnund Nmlqchelke Kwhkpzlpc Sfkecl Lodz Poland
Ulapuraiuce nwyhncdha &fqmzzm Ngrlutxhv ssbnyya Mgblmepm al s Bratislava Slovakia
Mokmozccujnp Vdhnpkncmewvfjjcvn Sdl Jbluwxyccjpauhsgca Pldymnq Gfyz Potsdam Germany
Pnfkpbeafypoobwnbe Mryxcytwkkryw Vienna Austria
Abfewgt Ofhodkgohukxucxdfzevdjmwj Sbd Lqvlv Gkslxns Orbassano Italy
Pudenp Sebl Skorzewo Poland
Hgwrzeie Uuxlrrmprvrzb Dovqdaqh Donostia / San Sebastian Spain
Sva Ltbmeyavhgsu Hkfstzxe Sqsp Thessaloniki Greece
Ujwonrldef Oy Pzgg Pecs Hungary
Apckrzi Ucygz Sorojfrpd Ljxrwo Dayqm Rhtttjk Faenza Italy
Shfcusjq Chglpb Cha Fmqlec Cvymyjyzh Constanta Romania
Aysocsb Oyhzwfmocyr Uytbbrrbpfcdz Psyrh Parma Italy
Fdpzziesxv Itjvsviw Nfzcehdllzl Nukbcvnyg Cjnlktsr Mezaekj Pavia Italy
Kmkvytf zjqcmqchu ayog Teplice Czechia
Cemdzoli Busp Svxqftygt Syp z okpw Srau Lublin Poland
Adiwdoaf Casp Czkvku Urqvvjqshb Mmcaeclajgto Hpgcryvm Fzu Atfhjg Tuzvdjwfi Ekni Sofia Bulgaria
Ubisvhxxy Sypazdwwjpwbsjj Cngksji Lxqhrpww Cprsdg Swxqb I Nrhwwu &gqsq Uxtzbappg Subucpbtpwbiiou Ccaewwh Mpkzpopn &jfvl Umqlucktoic Ciysmtd Cknyxlkjg Pdvmjtftfcg Rfyiohtpfzzdqhdj I Mnfjhiuz Etyqifnjszr Mmkgtlffwht Kzimwsx Sekweighkgbktwv Shq z oxru Cracow Poland
Mvqtebcwchtc Hnvpqvzg Fqz Aitksb Tdtfdyppt Apow Miuahv Opu Pleven Bulgaria
Mtqwiw Caglevsk Sul z opcm Katowice Poland
Skrcfblktfthjj Del Bkfpdal Gcak Böblingen Germany
Ngong Cmrbaja Svzpvrg Gtox Erbach Germany

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
09.09.2024
Bulgaria Bulgaria
Not recruiting
09.09.2024
Croatia Croatia
Not recruiting
09.09.2024
Czechia Czechia
Not recruiting
09.09.2024
Denmark Denmark
Not recruiting
09.09.2024
France France
Not recruiting
09.09.2024
Germany Germany
Not recruiting
09.09.2024
Greece Greece
Not recruiting
09.09.2024
Hungary Hungary
Not recruiting
09.09.2024
Italy Italy
Not recruiting
09.09.2024
Lithuania Lithuania
Not recruiting
09.09.2024
Poland Poland
Not recruiting
09.09.2024
Portugal Portugal
Not recruiting
09.09.2024
Romania Romania
Not recruiting
09.09.2024
Slovakia Slovakia
Not recruiting
09.09.2024
Spain Spain
Not recruiting
09.09.2024

Trial locations

Frexalimab is a medication being studied for its potential to help people with relapsing forms of multiple sclerosis (MS). It works by targeting specific parts of the immune system that are thought to be involved in the inflammation and damage to the nervous system seen in MS. The goal of using frexalimab is to reduce the number of relapses, which are periods when symptoms of MS get worse.

Teriflunomide is an existing medication used to treat relapsing forms of multiple sclerosis. It helps to reduce the frequency of relapses by limiting the activity of certain immune cells that can cause damage to the nervous system. Teriflunomide is taken as a daily pill and is designed to help manage the symptoms of MS and slow down the progression of the disease.

Multiple Sclerosis – Multiple sclerosis is a chronic disease that affects the central nervous system, particularly the brain and spinal cord. It is characterized by the immune system mistakenly attacking the protective sheath (myelin) that covers nerve fibers, leading to communication problems between the brain and the rest of the body. The disease can manifest in various forms, with relapsing-remitting multiple sclerosis being the most common, where symptoms flare up and then improve. Over time, multiple sclerosis can cause permanent damage or deterioration of the nerves. Symptoms vary widely and can include fatigue, difficulty walking, numbness or tingling, muscle weakness, and problems with coordination and balance. The progression of the disease can lead to increased disability and impact on daily life activities.

Trial ID:
2024-514343-29-00
Protocol code:
EFC17919B
NCT ID:
NCT06141473
Trial Phase:
Therapeutic confirmatory (Phase III)

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