Study on Long-Term Safety and Effectiveness of Ofatumumab for Patients with Relapsing Multiple Sclerosis

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What is this study about?

This clinical trial is focused on studying the long-term safety and effectiveness of a medication called ofatumumab in people with relapsing multiple sclerosis (RMS). 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. Ofatumumab is a type of medication known as a monoclonal antibody, which is designed to target specific cells in the immune system to help reduce the frequency of relapses in multiple sclerosis.

The purpose of this study is to evaluate how well ofatumumab is tolerated and how safe it is when used over a long period. Participants in the study will receive ofatumumab as an injection under the skin once every four weeks. The study will monitor participants for any side effects or changes in their health, including any changes in their laboratory test results or vital signs. The study will also track the number of relapses participants experience and any changes in their level of disability over time.

Participants will be followed for up to 240 weeks, which is about 4.5 years, to gather comprehensive data on the long-term effects of ofatumumab. The study aims to provide valuable information on the potential benefits and risks of using ofatumumab for managing relapsing multiple sclerosis, helping to inform future treatment options for this condition.

1 joining the study

Upon joining the study, the participant will begin receiving the medication ofatumumab.

The medication is administered as a subcutaneous injection every four weeks.

2 medication administration

The participant will receive ofatumumab at a dose of 20 mg.

This will continue every four weeks throughout the study duration.

3 monitoring and assessments

Regular monitoring will occur to assess safety and tolerability.

This includes checking for any adverse events and monitoring laboratory results and vital signs.

4 long-term evaluation

The study aims to evaluate the long-term safety and effectiveness of ofatumumab.

Participants will be monitored for up to 240 weeks, which is approximately 4.5 years.

5 end of study

The study is expected to conclude in September 2028.

Final assessments will be conducted to evaluate the overall outcomes of the treatment.

Who Can Join the Study?

  • The patient must have relapsing multiple sclerosis (RMS), which is a type of multiple sclerosis where symptoms come and go.
  • The patient must have participated in a previous study by Novartis that involved taking a medication called ofatumumab at a dose of 20 mg under the skin every 4 weeks.
  • The patient must have been an adult, meaning they were 18 years or older, during the previous study on RMS.
  • The patient must have completed the previous study while still taking the study medication.
  • The patient must provide written informed consent, which means they agree to participate in the study after being fully informed about it.
  • Both male and female patients are eligible to participate.

Who Cannot Join the Study?

  • Patients who have any other serious health conditions that could interfere with the study.
  • Patients who are pregnant or breastfeeding.
  • Patients who have had a recent infection that required treatment with antibiotics.
  • Patients who have received any other treatment for multiple sclerosis within the last month.
  • Patients who have a history of allergic reactions to similar medications.
  • Patients who have participated in another clinical trial within the last month.
  • Patients who have a history of drug or alcohol abuse.
  • Patients who have any condition that affects their immune system.
  • Patients who have been diagnosed with cancer in the past five years.
  • Patients who have any condition that affects their ability to understand or follow study instructions.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Zuyderland Medisch Centrum Stichting Geleen The Netherlands
Bellvitge University Hospital L'hospitalet De Llobregat Spain
Hospital Universitario Y Politecnico La Fe Valencia Spain
Nemocnice Pardubickeho kraje a.s. Pardubice Czechia
Medical University Of Vienna Vienna Austria
Hospital Clinico San Carlos Madrid Spain
Universitaetsklinikum Heidelberg AöR Heidelberg Germany
ZNS GmbH Zentrum fuer Neurologisch-Psychiatrische Studien Gutachten und medizinische Fortbildung Siegen Siegen Germany
Centre Hospitalier Universitaire De Lille Lille France
Universitaet Leipzig Leipzig Germany
Technische Universitaet Dresden Dresden Germany
Polyclinic Victus Zagreb Croatia

Other Sites

Site Name City Country Status
Pauls Stradins Clinical University Hospital Riga Latvia
F D Roosevelt University General Hospital Of Banska Bystrica Banska Bystrica Slovakia
KBC Zagreb Zagreb Croatia
Hopitaux Universitaires Pitie Salpetriere Paris France
Kistarcsai Flor Ferenc Korhaz Kistarcsa Hungary
MHAT National Heart Hospital EAD Sofia Bulgaria
Centre Hospitalier Universitaire De Nimes Nimes France
Universitair Ziekenhuis Gent Gent Belgium
Hospital Universitario Puerta Del Mar Cadiz Spain
University Hospital Bratislava Bratislava Slovakia
Lietuvos sveikatos mokslu universiteto ligonine Kauno klinikos Kaunas Lithuania
Univerzitna Nemocnica Martin Martin Slovakia
Krajska zdravotni a.s. Teplice Czechia
Fakultna Nemocnica Trnava Trnava Slovakia
Hospital Beatriz Angelo Loures Portugal
CCAB Centro Clinico Academico Braga Associacao Braga Portugal
Region Stockholm – SLSO Stockholm Sweden
Copernicus Podmiot Leczniczy Sp. z o.o. Gdansk Poland
Unidade Local De Saude De Entre O Douro E Vouga E.P.E. Santa Maria Da Feira Portugal
Unidade Local De Saude De Matosinhos E.P.E. Senhora Da Hora Portugal
Latvijas Juras medicinas centrs AS Riga Latvia
Drammen Sykehus Drammen Norway
NeuroPoint Gesellschaft fur vorbeugende Gesundheitspflege GmbH Ulm Germany
Wromedica I Bielicka A Strzalkowska s.c. Wroclaw Poland
Ma-Lek Clinical Sp. z o.o. Katowice Poland
Resmedica Sp. z o.o. Kielce Poland
St. Josef-Hospital Bochum Germany
401 General Military Hospital Of Athens Athens Greece
Multiprofile Hospital For Active Treatment In Neurology And Psychiatry St. Naum EAD Sofia Bulgaria
Nemocnice Jihlava prispevkova organizace Jihlava Czechia
University General Hospital Of Thessaloniki Ahepa Thessaloniki Greece
Clinical Medical Center Osijek Osijek Croatia
Diagnostic-consultative center “Aleksandrovska” EOOD Sofia Bulgaria
Bajcsy-Zsilinszky Korhaz Es Rendelointezet Budapest Hungary
Odense University Hospital Odense Denmark
Hospital Clinic De Barcelona Barcelona Spain
Vilniaus universiteto ligonine Santaros klinikos VšĮ Vilnius Lithuania
Tartu University Hospital Tartu Estonia
Hospital Da Luz S.A. Lisbon Portugal
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
Hospital Universitario De Cruces Barakaldo Spain
Instytut Psychiatrii I Neurologii Warsaw Poland
Fakultni Nemocnice Kralovske Vinohrady Prague Czechia
Hospital Universitario Quironsalud Madrid Pozuelo De Alarcon Spain
University Clinical Hospital Virgen De La Arrixaca Murcia Spain
Centre Hospitalier Universitaire De Montpellier Montpellier France
Fakultni Nemocnice U Sv Anny V Brne Brno-Stred Czechia
Justus-Liebig-Universitaet Giessen Giessen Germany
Laane-Tallinna Keskhaigla AS Pohja-Tallinna Linnaosa Estonia
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Nice Nice France
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
Jahn Ferenc Del-Pesti Korhaz Es Rendelointezet Budapest Hungary
Neurocentrum Bydgoszcz Sp. z o.o. Bydgoszcz Poland
University Hospital Olomouc Olomouc Czechia
Rigshospitalet Copenhagen Denmark
Mehilaeinen Oy Helsinki Finland
University Of Pecs Pecs Hungary
Centrum Medyczne Medyk Sp. z o.o. Rzeszow Poland
Nowe Techniki Medyczne Szpital Specjalistyczny Imienia Swietej Rodziny Sp. z o.o. Glogow Malopolski Poland
Hospital Universitario Puerta De Hierro De Majadahonda Majadahonda Spain
Queen Silvia Childrens Hospital – Sahlgrenska University Hospital – Vaestra Goetalandsregionen Gothenburg Sweden
Kardiocentrum Nitra s.r.o. Nitra Slovakia
Multi-profile Hospital for Active Treatment Heart and Brain EAD Pleven Bulgaria
Fakultni Thomayerova nemocnice Prague Czechia
University Of Szeged Szeged Hungary
S-Medicon Egészségügyi Szolgáltató Kft. Budapest Hungary
Suomen Terveystalo Oy Tampere Finland
Hbzexrnb Sehco Csflujfs Igy Salt Spain
Uwunwcnzbpxttjjdjicqp Eqtfd Ajl Essen Germany
Hpjwjqxt Uzdvetxvxnmzv Do Ld Ppjzkyex Madrid Spain
Szfiaifgmfm Pzbespnoo Spvusvp Kbrjuwdfd Nz 1 Ibevzneumeylhmevke Szspykt Sekxuwfpv Uaqtzxzqvhlp Mnbszbgsuz W Knshjdrnzo Zabrze Poland
Nrzmvtybj sjwhxz Slezska Ostrava Czechia
Mqguldnc Ssfnasw Hamburg Germany
Cbiafap Nlcefksbfx Kmkeswjlv Smstkv Lodz Poland
Cthllubdj Uxuxvqkdzewycd Snqdkmved Woluwe-Saint-Lambert Belgium
Nkavpsonmgtw Bdelglrdt Bielefeld Germany
Knvjceus btepfdda cnlwve Rsmibc (cjniphvv Huxfwahd Coyxhh Rpbykhq Rijeka Croatia
Atjrizfmw Usz Amsterdam The Netherlands
Elbdcfm Ubkpisfuardz Mmllghg Cqesvkd Ruvqdlruh (rdllrah Mrk Rotterdam The Netherlands
Rpghr Achnckyx krqijffw uymuzkbaotubv sqxzrfpt Stp Riga Latvia
Hnflawzz Uuaayndspkenx Dywyjdgu Donostia / San Sebastian Spain
Kdomgxjr Bbjhehlt Gwbp Bayreuth Germany
Kewfzbrb dwj Uqullxvpapvt Midrjwje Avi Munich Germany
Ufryjwpzkharhy Cmbbzza Kqzrifcki Gdansk Poland
Hyysqsno Dd La Sklab Cxuy I Sbyu Pfz Barcelona Spain
Upetdfljnf Oy Afryohb Edegem Belgium
Mblkios Cjwyhi Mprlzhbnmc Putphy Ozg Pleven Bulgaria
Hxjxcwwi Vkea dbdurrac Barcelona Spain
Uxh Miagpfs Tdhold Kjsd Budapest Hungary
Htzurizu Ufpfoycvmadend Sucwncpfby &vomtkc Hxgvetn dd Hmtcjnvzsiv STRASBOURG, Alsace France

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
30.01.2019
Belgium Belgium
Not recruiting
30.01.2019
Bulgaria Bulgaria
Not recruiting
30.01.2019
Croatia Croatia
Not recruiting
30.01.2019
Czechia Czechia
Not recruiting
30.01.2019
Denmark Denmark
Not recruiting
30.01.2019
Estonia Estonia
Not recruiting
30.01.2019
Finland Finland
Not recruiting
30.01.2019
France France
Not recruiting
30.01.2019
Germany Germany
Not recruiting
30.01.2019
Greece Greece
Not recruiting
30.01.2019
Hungary Hungary
Not recruiting
30.01.2019
Latvia Latvia
Not recruiting
30.01.2019
Lithuania Lithuania
Not recruiting
30.01.2019
Norway Norway
Not recruiting
30.01.2019
Poland Poland
Not recruiting
30.01.2019
Portugal Portugal
Not recruiting
30.01.2019
Slovakia Slovakia
Not recruiting
30.01.2019
Spain Spain
Not recruiting
30.01.2019
Sweden Sweden
Not recruiting
30.01.2019
The Netherlands The Netherlands
Not recruiting
30.01.2019

Trial locations

Investigated drugs:

Ofatumumab is a medication used in this clinical trial to treat individuals with relapsing multiple sclerosis (RMS). It is administered as an injection under the skin once every four weeks. The purpose of this study is to assess the long-term safety, tolerability, and effectiveness of ofatumumab for patients with RMS.

Investigated diseases:

Relapsing Multiple Sclerosis (RMS) – Relapsing multiple sclerosis is a chronic disease affecting the central nervous system, characterized by episodes of new or worsening neurological symptoms. These episodes, known as relapses, are followed by periods of partial or complete recovery. The disease can lead to symptoms such as fatigue, difficulty walking, numbness, and vision problems. Over time, the frequency and severity of relapses may vary, and some individuals may experience a gradual worsening of symptoms. The exact cause of RMS is not fully understood, but it involves an immune system attack on the protective covering of nerves. This damage disrupts communication between the brain and the rest of the body.

Trial ID:
2023-507906-15-00
Protocol code:
COMB157G2399
Trial Phase:
Therapeutic confirmatory (Phase III)

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