Phase 2 Multiple Sclerosis Trial, Recruiting NCT07074886 Sponsor: Hoffmann-La Roche Condition: Multiple Sclerosis
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Phase 2 Multiple Sclerosis Trial, Recruiting

NCT07074886
Recruiting Phase 2

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:

  • You have been diagnosed with relapsing multiple sclerosis (RMS) or primary progressive multiple sclerosis (PPMS), confirmed using standard MS diagnostic guidelines
  • Your level of physical disability, measured by a standard MS scale, falls within a mild-to-moderate range (a score between 0 and 6.5 out of 10) at the time of your screening appointment

Who may not be able to join:

  • You received a specific type of MS treatment called an "anti-CD20" therapy (such as ocrelizumab) less than 2 years ago
  • You received an anti-CD20 therapy more than 2 years ago, but your B-cell levels (a type of immune cell) are still lower than normal, or you stopped that treatment because of safety concerns
  • You have a history of a serious brain infection called progressive multifocal leukoencephalopathy (PML), either confirmed or suspected (confirm with trial site)
  • You have had any form of cancer, including blood cancers or solid tumours, within the past 10 years
  • Your immune system is significantly weakened for any reason
  • You have had a previous allergic reaction to ocrelizumab or any of its ingredients
  • You have had a severe allergic reaction (including anaphylaxis) to similar types of antibody-based medicines in the past
  • You have another condition that requires ongoing treatment with steroid or immune-suppressing medicines
  • You have a serious, uncontrolled condition affecting your heart, lungs, kidneys, liver, hormone system, or digestive system, or any other significant health condition
  • You do not have a usable vein for receiving intravenous (IV) treatment
  • You have previously been treated with cladribine, atacicept, or alemtuzumab (specific MS or immune-related medicines)
  • You have previously had a bone marrow or stem cell transplant
  • You have any history of organ transplantation or have taken anti-rejection medication
  • Your screening blood tests show a current or past hepatitis B infection that has not been fully treated

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 15 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Clinical Trials, Hoffmann-La Roche

Phone: 888-662-6728 (U.S.)

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
13 November 2025
Est. completion
31 January 2027

Where this trial is recruiting

🇦🇷 Argentina 🇧🇷 Brazil 🇫🇷 France 🇩🇪 Germany 🇮🇹 Italy 🇲🇽 Mexico 🇵🇱 Poland 🇪🇸 Spain 🇺🇸 United States

Primary endpoints

Area Under the Serum Concentration-time Curve Over the First 12 Weeks Post-dose (AUC0-12W) of Ocrelizumab; Maximum Serum Concentration (Cmax) of Ocrelizumab

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov