Phase 1 Multiple Sclerosis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with Primary Progressive Multiple Sclerosis (PPMS) or Relapsing Multiple Sclerosis (RMS), confirmed using a specific set of diagnostic guidelines called the McDonald 2017 criteria
- People whose level of physical disability, as measured by a standard MS scoring tool called the EDSS, falls between 0 and 6.5 at the time of initial assessment
Who may not be able to join:
- People who received a type of medication known as an anti-CD20 therapy (including ocrelizumab) less than 2 years before the initial screening assessment
- People who have an active or suspected infection at the time of screening or at the start of the trial (minor nailbed infections are excepted), or who have had a serious infection requiring hospital care or intravenous antibiotics within the past 8 weeks, or oral antibiotics within the past 2 weeks
- People with a confirmed or suspected history of a serious brain infection called progressive multifocal leukoencephalopathy (PML) (confirm with trial site)
- People who have had any form of cancer, including blood cancers or solid tumours, within the 10 years before screening
- People whose immune system is significantly weakened for any reason
- People who have another condition that would require long-term use of steroid tablets or immune-suppressing medicines during the trial
- People with serious, uncontrolled conditions affecting the heart, lungs, kidneys, liver, hormonal system, or digestive system, or any other significant health condition that may prevent safe participation
- People for whom a standard intravenous (IV) line cannot be placed in an arm or hand vein
- People who have previously been treated with the medications cladribine, atacicept, or alemtuzumab
- People who have taken the medications fingolimod, siponimod, ponesimod, or ozanimod within 6 weeks before the trial start date
- People who have previously had a bone marrow transplant or stem cell transplant of any kind
- People with any history of organ or tissue transplantation, or who have taken anti-rejection medication
- People whose screening blood tests show active, dormant, or inadequately treated hepatitis B infection
- People who are known to be sensitive or intolerant to ocrelizumab or any of its ingredients
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Clinical Trials, Hoffmann-La Roche
Phone: 888-662-6728 (U.S. Only)
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
Number of Participants With Adverse Events (AEs)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.