Study Comparing ABP 692 and Ocrelizumab for Patients with Relapsing-Remitting Multiple Sclerosis

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What is this study about?

This clinical trial is focused on studying a condition known as Relapsing-Remitting Multiple Sclerosis (RRMS). This is a type of multiple sclerosis where patients experience episodes of new or increasing symptoms followed by periods of partial or complete recovery. The study will compare two treatments: ABP 692 and Ocrevus (also known as ocrelizumab), which are both given as an infusion, meaning they are administered directly into the bloodstream through a vein.

The purpose of the study is to compare how these two treatments work in the body, their effects on the disease, and their safety. Participants will receive either ABP 692 or Ocrevus, and the study will monitor how the treatments affect the number of new active brain lesions, which are areas of damage in the brain that can be seen using a special imaging technique called MRI (Magnetic Resonance Imaging). The study will last for about 48 weeks, with regular check-ups to assess the treatments’ effects and safety.

Throughout the study, participants will receive regular infusions and undergo various assessments to monitor their health and the progression of their condition. The goal is to determine if ABP 692 is as effective and safe as Ocrevus in treating RRMS. This information could help improve treatment options for people living with this condition.

1 initial assessment

The study begins with an initial assessment to confirm eligibility. This includes a diagnosis of relapsing-remitting multiple sclerosis (RRMS) according to specific criteria, a disability score between 0 and 5.5, and recent activity of the condition.

The participant must be neurologically stable, with no relapses for at least 28 days before starting the trial.

2 randomization

Participants are randomly assigned to receive either ABP 692 or Ocrevus (ocrelizumab). This process is double-blind, meaning neither the participant nor the researchers know which treatment is being administered.

3 treatment administration

The treatment involves an intravenous infusion of the assigned medication. The specific product used is either Ocrevus 300 mg concentrate for solution for infusion or ABP 692.

The infusion is administered according to the study protocol, which includes monitoring the participant’s response and any side effects.

4 monitoring and follow-up

Participants are monitored for the pharmacokinetics (how the drug is processed in the body) and pharmacodynamics (the effects of the drug) over a period of 24 weeks.

Regular assessments are conducted to track the suppression of new active brain lesions using MRI scans at weeks 4, 8, 12, 16, 20, and 24.

5 completion of study

The study is estimated to conclude by July 2, 2027. Participants will have completed all required assessments and treatments by this time.

Who Can Join the Study?

  • The patient must have a diagnosis of Relapsing-remitting Multiple Sclerosis (RRMS), which is a type of multiple sclerosis where symptoms come and go.
  • The patient must meet the revised McDonald Criteria 2017, which are guidelines used to diagnose multiple sclerosis.
  • The patient must have a score on the Expanded Disability Status Scale (EDSS) between 0 and 5.5. This scale measures the level of disability in people with multiple sclerosis.
  • There must be evidence of recent multiple sclerosis activity, as defined by the study protocol.
  • The patient must be neurologically stable, meaning they have not had a relapse, or worsening of symptoms, for 28 days or less before joining the study.
  • The study is open to both male and female participants.
  • The study is for adults aged 18 years and older.

Who Cannot Join the Study?

  • Patients with any other type of Multiple Sclerosis besides Relapsing-remitting Multiple Sclerosis cannot participate. Multiple Sclerosis is a condition that affects the brain and spinal cord, and relapsing-remitting means it comes and goes.
  • Patients who are not within the specified age range for the study cannot participate. The age range is determined by the study organizers.
  • Patients who are part of a vulnerable population, which means they might need special protection or care, cannot participate.
  • Patients who do not meet the health requirements set by the study organizers cannot participate. These requirements ensure the safety and effectiveness of the study.

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
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Karolinska University Hospital Solna Sweden
Hospital General Universitario Gregorio Maranon Madrid Spain
Nemocnice Jihlava prispevkova organizace Jihlava Czechia
curiositas ad sanum Studien und Beratungs GmbH Haag in Obb Germany
Azienda Unita Sanitaria Locale Di Bologna Bologna Italy
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
University Medical Center Ljubljana Ljubljana Slovenia
Klaipedos universiteto ligonine VšĮ Klaipeda Lithuania
Noorderhart Pelt Belgium
Resmedica Sp. z o.o. Kielce Poland
Krakowska Akademia Neurologii Sp. z o.o. Cracow Poland
Neuropraxis Muenchen Sued Unterhaching Germany
Ucjglwjdon Mjdvumfswgvt Hlhbnrkl Fbh Apwqec Tlxfiamwo Atz Etnksljal Mlezwjvr N I Pobxtjk Sofia Bulgaria
Mpeyrhq Cjaono Hqtc Eogs Sofia Bulgaria
Hpprjoff Ccpvnu Dn Boennqrvy Barcelona Spain
Sfzovmireed Phzcudbgq Zxoonp Oukyfj Zhhtuycwol Sfsuaqt Umggawwdwzzok W Kkpjmcnn Cracow Poland
Usjajsyrsyttlxpgoofyr Hdjrayblbg Ahe Heidelberg Germany
Jhnyuditcirdryijodxydhefsb Gtpiypo Giessen Germany
Uajfdffent Op Azjwgzs Edegem Belgium
Ckqfti Hxstuopajzr Ugellnzlpoksa Dx Nezvq Nimes France
Uremzfxrdmebuzgkoqdpt Elhfr Acg Essen Germany
Acvnkmql Zksrrsyqed Dhlgd Roeselare Belgium
Qjyqr Sfnijh Csrrcjxza Hrcmadka &lomjpr Ssovypxblvg Uztldusczy Hjaacwbw &fkrrad Vywoozq Gyywhcpubueszzcrdx Gothenburg Sweden
Fgjxrarw Nqtgjxyol Tkojvd Trnava Slovakia
Uwuokxrlttlhvykemnwlp Ltsgtxy Arw Leipzig Germany
Kid Zwnghf Zagreb Croatia
Allodbx Otejhuuxodjnqpzwkwkxjmidg Pyauhpalkkc Gw Rvbvqhvlynwr Muyuk Dm Cirkwun Catania Italy
Mdekcefpyrpn Hawqceln Fjy Aeysqh Tqkilpiqo Iq Nwwmtaygj Axq Pvitcnbwkr Sob Namn Efj Sofia Bulgaria
Ddgfsqoucul Afs Cwlqjjgmwaft Cwkkzr Csmvcl Lmtk Sofia Bulgaria
Ahbedtw Cxzhdhf Scualc Bucharest Romania
Huywfmwf Szmeb Cwhvvxiw Itp Salt Spain
Ctqn Dd Clfz Imwx Skjwef Milan Italy
Cemiyfc Nptmdbjxyq Khhqhjpox Slicsa Lodz Poland
Hrwbtljy dt Dpiqz Denia Spain
Bcwuqkvi Chfhve Sfymso Constanta Romania
Ejatqpe sv re ow Bratislava Slovakia
Nuaoftdvxy Sal z oeln sbyyg Katowice Poland
Amxuirg Otlhmcziuhi Unyhzwlfetmev Scejze Siena Italy
Atqyvp Uqmxxtighq Hjdrhtnt Aarhus Denmark
Fjthnxut Nzbskiqdn U Sm Amsq V Btut Brno-Stred Czechia
Hujrhtby Vwampu Pbcwwf Svh Aucshfc Malaga Spain
Nfhjtbxmoxud Bnmkbtpxp Slp z ofoo Bydgoszcz Poland
Rmmckbdjlepwhi Glostrup Denmark
Srfmyjqi Cdayed Cus Fcdbsq Csnqujapg Constanta Romania
Hzuuwmce Agphkp Crliserzk Vigo Spain
Cptvvr Hjuphtlhapk Usuhzdjdlwiah Rhlpx Reims France
Acpssav Ojtuujfjuipbwcgphtazdffif Srra Ahlzf Rome Italy
Ubmyrvidor Hkjhujmq Baeyrninhh Bratislava Slovakia
Ldpzhgio sszaenzab mzrnwm ukcldhglzibf lqyltmmr Kuwiw kkesbbvv Kaunas Lithuania
Mxv Crcggkww Rjfmclgt Pupyegt Bj Pmpiuc Warsaw Poland
Uwgmqisxmgijm Kfhumgap Cjyqde Mygjfwr Maribor Slovenia
Kxinbgf zdkoggrlr anay Teplice Czechia
Klypcsrvh Fbrhkndtx Haiqwdk Gmdb Hamburg Germany
Hhymryrl Uyyfhzpmsnhep Dq Ppenk Aijdleyhvs Valencia Spain
Vmvmibx Gbowk I Czrjbdyzs Smg jd Bydgoszcz Poland
Ftpmsvnzlr Iilqsnul Gd Guufzf Di Crimnb Cefalu' Italy
Mqyzdyxpuqvur Hpmntvkz fvg Azersg Txvzfurwz Hlifn aby Bvarn Eeq Pleven Bulgaria
Mxfged Cxdrfxbg Suv z oxgr Katowice Poland
Nfhsyzfsqroz Sar z oxeq Warsaw Poland
Zwajhuf fgnp kkbdwbxbf Fsqczhqvc Dqu Is Srnezvo Gvpg Bad Homburg Germany
Sqkwkcoqavgarg Duf Byctlss Gsyh Böblingen Germany
Nlrfeiuwwa Ra Ccrofxa sjvbib Hradec Kralove Czechia
Mcylpfqd Sdjutsw Hamburg Germany
Ziv Gact Zxdecdu firi Nyhgicftevcpujuqkqxh Snscqha Gifmwrbrd uhn mpkdpyvuzytw Frijtyokbuh Szvilf Siegen Germany

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Not yet recruiting
15.03.2025
Bulgaria Bulgaria
Not recruiting
15.03.2025
Croatia Croatia
Not recruiting
15.03.2025
Czechia Czechia
Not recruiting
15.03.2025
Denmark Denmark
Not recruiting
15.03.2025
France France
Not recruiting
15.03.2025
Germany Germany
Not recruiting
15.03.2025
Italy Italy
Not recruiting
15.03.2025
Lithuania Lithuania
Not yet recruiting
15.03.2025
Poland Poland
Not recruiting
15.03.2025
Romania Romania
Not recruiting
15.03.2025
Slovakia Slovakia
Not recruiting
15.03.2025
Slovenia Slovenia
Not recruiting
15.03.2025
Spain Spain
Not recruiting
15.03.2025
Sweden Sweden
Not yet recruiting
15.03.2025

Trial locations

Investigated Drugs:

ABP 692 is an investigational medication being studied for its effects on relapsing-remitting multiple sclerosis. It is being compared to an existing treatment to see if it works in a similar way in the body and has similar effects on the disease.

Ocrevus® (Ocrelizumab) is a medication already approved for the treatment of relapsing-remitting multiple sclerosis. It works by targeting specific cells in the immune system to reduce inflammation and prevent new brain lesions, which are common in multiple sclerosis. This study is comparing the effects of ABP 692 to Ocrevus® to ensure they are similar in terms of how they work and their safety profiles.

Relapsing-remitting Multiple Sclerosis – This is a form of multiple sclerosis characterized by episodes of new or increasing neurological symptoms, known as relapses, followed by periods of partial or complete recovery. During a relapse, individuals may experience symptoms such as vision problems, muscle weakness, or coordination difficulties. These symptoms can vary in severity and duration. After a relapse, there is a remission phase where symptoms may improve or disappear entirely. However, over time, some symptoms may persist and accumulate, leading to gradual disability. The disease course is unpredictable, with the frequency and severity of relapses varying among individuals.

Trial ID:
2024-512914-16-00
Protocol code:
20230309
Trial Phase:
Therapeutic confirmatory (Phase III)

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