Study on the Effectiveness and Safety of Ocrelizumab for Adults with Primary Progressive Multiple Sclerosis

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What is this study about?

This clinical trial is focused on studying a condition known as Primary Progressive Multiple Sclerosis (PPMS). This is a type of multiple sclerosis where the disease gradually worsens over time without any periods of improvement. The study is evaluating a treatment called Ocrelizumab, which is given as a solution through an intravenous infusion, meaning it is administered directly into the bloodstream through a vein.

The purpose of the study is to assess how effective and safe Ocrelizumab is for adults with PPMS. Participants in the study will receive either Ocrelizumab or a placebo, which is a substance with no active medication. The study will monitor the time it takes for participants to experience a progression in their symptoms, such as worsening hand function or an increase in disability, as measured by specific tests. These tests include the 9-Hole Peg Test (9-HPT), which measures hand dexterity, and the Expanded Disability Status Scale (EDSS), which assesses disability in people with multiple sclerosis.

Throughout the study, participants will undergo regular MRI scans to check for changes in the brain and spinal cord. The study will also track any side effects or adverse events that occur. The trial is designed to last for several years, allowing researchers to gather comprehensive data on the long-term effects of Ocrelizumab in treating PPMS.

1 joining the study

Upon joining the study, the diagnosis of primary progressive multiple sclerosis (PPMS) is confirmed according to specific criteria.

Eligibility is assessed based on factors such as the Expanded Disability Status Scale (EDSS) score and disease duration.

2 screening phase

During the screening phase, magnetic resonance imaging (MRI) scans are conducted to detect specific brain lesions.

Laboratory tests are performed to check for certain proteins in the cerebrospinal fluid.

3 randomization

Participants are randomly assigned to receive either Ocrevus or a placebo.

The study is double-blind, meaning neither the participants nor the researchers know who receives the actual medication.

4 treatment administration

Ocrevus is administered as an intravenous infusion.

The dosage is 300 mg, and the infusion is given at specified intervals throughout the study.

5 monitoring and assessments

Regular assessments are conducted to monitor the progression of the disease.

These include tests like the 9-Hole Peg Test (9-HPT) and evaluations of the EDSS score.

6 safety evaluations

The study monitors for any adverse events or side effects related to the treatment.

Laboratory tests are repeated to ensure the safety of the participants.

7 study completion

The study is expected to conclude by September 2030.

Final assessments are conducted to evaluate the overall efficacy and safety of the treatment.

Who Can Join the Study?

  • Must have a diagnosis of Primary Progressive Multiple Sclerosis (PPMS) according to specific medical guidelines.
  • Must have an EDSS score between 3.0 and 8.0. The EDSS score is a way to measure disability in people with multiple sclerosis.
  • The disease must have started less than 20 years ago if the EDSS score is between 7.0 and 8.0, less than 15 years ago if the EDSS score is between 5.5 and 6.5, and less than 10 years ago if the EDSS score is 5.0 or lower.
  • Must have a history or current presence of certain findings in the cerebrospinal fluid, which is the fluid around the brain and spine. This includes an elevated IgG index or the presence of IgG oligoclonal bands, which are specific proteins.
  • Must complete a test called the 9-HPT in more than 25 seconds. The 9-HPT is a hand function test where you place pegs in holes.
  • Must have stable neurological health for at least 30 days before starting the study.
  • Both males and females can participate.

Who Cannot Join the Study?

  • Patients with any other type of multiple sclerosis besides Primary Progressive Multiple Sclerosis (PPMS) cannot participate. PPMS is a form of multiple sclerosis where symptoms gradually worsen over time.
  • Patients who have had recent infections or are currently experiencing an infection are not eligible.
  • Individuals with a history of cancer, except for certain types of skin cancer, are excluded.
  • Patients who have received certain treatments for multiple sclerosis in the past may not be eligible.
  • Women who are pregnant or breastfeeding cannot participate in the study.
  • Patients with severe heart problems or other serious health conditions are not eligible.
  • Individuals who have had an allergic reaction to similar medications in the past are excluded.
  • Patients who are unable to undergo MRI scans, which are imaging tests used to look at the brain and spinal cord, cannot participate.
  • Individuals who are participating in another clinical trial at the same time are not eligible.

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
Ospedale San Raffaele S.r.l. Milan Italy
Centre Hospitalier Universitaire De Nantes Nantes France
Unidade Local De Saude De Loures-Odivelas EPE Loures Portugal
Noorderhart Pelt Belgium
Copernicus Podmiot Leczniczy Sp. z o.o. Gdansk Poland
Resmedica Sp. z o.o. Kielce Poland
Cfotvbfep Uhndszszerwluy Siucczyog Woluwe-Saint-Lambert Belgium
Hppfrims Vdlj doawuxli Barcelona Spain
Aieuzfsqcr Poxenpqn Hacputrg Dw Mkrhnlmsv Marseille France
Httqikfn Cqtvsp Dl Bdfwolpyn Barcelona Spain
Inwsx Orlgdgun Pvdoqgnttxf Szv Mijuhbu Genoa Italy
Umrlzzcgut Czrhogbc Hjxyntfv Vognkx Dx La Alosguje Murcia Spain
Chjn Dx Nhgod Vandoeuvre Les Nancy France
Chlgmu Hheaoxonww Ukjshdbgwkrli Dp Srfhn Aapevrk Eiyrho Porto Portugal
Uwflatpuil Od Aadhkwk Edegem Belgium
Ciwgsb Hkaujpxavct Uheqzgkkmzizt Do Ngsop Nimes France
Cwlplg Hgyeibqnnth Llvc Sxb Pierre Benite France
Hfnhgprv Uwfldulnqawer Paknnc Dh Hjnnnt Db Mpnxnskxkbi Majadahonda Spain
Pmguzvcjn Haicmxjb Bordeaux France
Cwzd Ckesdw Cipodfh Adxuijgrn Bchzw Ajaarkgctq Braga Portugal
Cuuukefd Hwleyoqxyttl Udqjbwlttinde Ds Vcag Vigo Spain
Htvkvatv Unjuibgbiohwmg Shibfbqgdi &yvolsc Hdtzdgi do Hjhsutqrpxz STRASBOURG, Alsace France
Khc Zmmebg Zagreb Croatia
Mihqlscduafn Hiomllvy Fcr Aowwhr Tyvipfypl Ij Nuppvmunt Aso Pnshcnbqit Sfn Nnmk Edt Sofia Bulgaria
Mnj Pbtasis Sio z ophm Poznan Poland
Ncyloxxy Zkstnjqwl I Wzyichghv Ssh jp Katowice Poland
Ckfoowyj Mrcszbz Ciocig Ovvmkj Osijek Croatia
Uirnyaafuwmqd Sasivbp Kzaxyetdr W Btfqrykhtzj Bialystok Poland
Sydlioen Jnektour Dr Uhvxany Dlcd Deva Romania
Culxgqz Nxixmxcrlg Kvfncixmi Sufgxw Lodz Poland
Algbewj Owteiefgvmhkxladiyxeoyvjn Sls Lwkrd Gifezrm Orbassano Italy
Hbeepvjh Ukihnsziraopp Qcqumpufgpk Mqzejf Pozuelo De Alarcon Spain
Ndppbqpgyxha Bhymgidjd Seg z oqfg Bydgoszcz Poland
Mfqasoaj Mqyusgw Aqtqxvj Pleven Bulgaria
Cjenktm Mvwmeqxm Mkuig Sab z ovzk Rzeszow Poland
Sxljudhm Cywjsw Cll Fmfmva Crxcuzzmy Constanta Romania
Audhoau Otchltpqguvdlpzvaelulwjci Srie Azsel Rome Italy
Fwlmovvrei Iaxavlpr Nnpkmeqkqyk Nwohnhoeh Cmahmpig Mzzzisi Pavia Italy
Etmrudgwx Sma z oemf Szczecin Poland
Fjbpvrrzgr Idtfvjov Gi Gmrhpz Dv Cutdlf Cefalu' Italy
Chy Szgub Lrvp Torres Vedras Portugal
Ewfvtfuco Iblbspnkj Fhx Csjiwievulphof Dcttvauq Adb Tgqpreihzp Targu Mures Romania
Wrojmktsns Szcqezv Shnsxfyrlvkomkg W Omgzxrkjp Olsztyn Poland
Mqyuobawabox Hdoqjcfz Fis Adwdyu Tztpdtmsz Aivm Msocyp Ogt Pleven Bulgaria
Mykzgb Ciqdvwbi Sxm z ondp Katowice Poland
Stlgabcfmgi Pqkcdeebe Zhpnsq Oacrxd Zxqinqgvnx Wrycdurknb Sbhindy Sqolyfkihsojdaf No 3 W Ragofcp Rybnik Poland
Oyxc Bfyrwuo Vmxgwrmp Varazdin Croatia
Nndxccuaqosh Sfd z opeq Warsaw Poland
Czaaqc Suvrxgpyv Sxprwu Campulung Romania
Savueif Ujykhnjxphntm w Khutytid Cracow Poland
Inzbtuaxfoly Pkotjstm Lgejjuic Pthrf dd hadb nx mffo Klsqav Rnjjtm Lublin Poland
Evu Ijmtzbxh Mzbsazrs Sohi Poznan Poland
Mgkj Izeba Cexqapudjg Akhk Phpkqkfqv Sghbklltesv sksm Pruszkow Poland

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Not recruiting
30.10.2019
Bulgaria Bulgaria
Not recruiting
30.10.2019
Croatia Croatia
Not recruiting
30.10.2019
France France
Not recruiting
30.10.2019
Italy Italy
Not recruiting
30.10.2019
Poland Poland
Not recruiting
30.10.2019
Portugal Portugal
Not recruiting
30.10.2019
Romania Romania
Not recruiting
30.10.2019
Spain Spain
Not recruiting
30.10.2019

Trial locations

Ocrelizumab is a medication being studied for its effectiveness and safety in treating adults with primary progressive multiple sclerosis. It works by targeting specific cells in the immune system that are believed to play a role in the progression of multiple sclerosis. The goal of the trial is to see if ocrelizumab can slow down the worsening of symptoms in patients compared to those who do not receive the treatment.

Primary Progressive Multiple Sclerosis (PPMS) – This is a form of multiple sclerosis characterized by a gradual worsening of neurological function from the onset of symptoms, without early relapses or remissions. Unlike other types of multiple sclerosis, PPMS progresses steadily over time, although the rate of progression can vary among individuals. Symptoms may include problems with walking, muscle stiffness, and weakness, as well as issues with balance and coordination. Some individuals may also experience cognitive changes, such as difficulties with memory and concentration. The disease primarily affects the spinal cord and brain, leading to a gradual decline in physical abilities. The exact cause of PPMS is unknown, but it involves an immune-mediated process that damages the protective covering of nerve fibers.

Trial ID:
2023-505980-36-00
Protocol code:
WA40404
Trial Phase:
Therapeutic confirmatory (Phase III)

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