100 Participants NeededMy employer runs this trial

Ocrelizumab for Multiple Sclerosis

(OSSIA Trial)

Recruiting at 12 trial locations
RS
RS
Fr
Overseen ByFastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
Age: 18+
Sex: Any
Trial Phase: Phase 4
Sponsor: Genentech, Inc.
Must be taking: Anti-CD20 therapy
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new method of administering ocrelizumab, a treatment for multiple sclerosis (MS), by injecting it under the skin instead of into a vein. Researchers aim to evaluate the effectiveness, safety, and patient satisfaction of this method. The trial includes individuals with either relapsing or primary progressive MS who have previously used a similar type of medicine and are switching treatments for reasons other than a poor response. Those diagnosed with MS and transitioning from a similar treatment may find this trial suitable. As a Phase 4 trial, the research focuses on understanding how this already FDA-approved and effective treatment can benefit more patients.

Do I have to stop taking my current medications for the trial?

The trial does not specify if you need to stop taking your current medications, but it does require that you switch from another specific multiple sclerosis therapy to ocrelizumab. It's best to discuss your current medications with the trial team.

What is the safety track record for this treatment?

Research has shown that ocrelizumab, a treatment for multiple sclerosis (MS), is generally safe. Studies have treated over 6,000 patients with ocrelizumab, providing extensive information about its effects. Adverse events occur at a rate of about 230 per 100 patient-years, indicating that while some people might experience side effects, they are usually manageable. Infections occur at a rate of 71 per 100 patient-years, and serious side effects are less common, occurring about 8 times per 100 patient-years. These findings suggest that most people tolerate ocrelizumab well. It also maintains a favorable benefit-risk balance, meaning the benefits typically outweigh the risks.12345

Why are researchers enthusiastic about this study treatment?

Ocrelizumab is unique because it targets CD20-positive B cells, a specific type of immune cell involved in the progression of multiple sclerosis (MS). While most MS treatments, like interferons and glatiramer acetate, work by modulating the immune system, Ocrelizumab directly depletes these B cells, potentially reducing the immune response that damages nerve cells. Researchers are excited about Ocrelizumab because it has shown promising results in slowing down the progression of MS with a different mechanism of action, and it is administered subcutaneously, which may offer more convenience compared to intravenous options.

What is the effectiveness track record for ocrelizumab in treating multiple sclerosis?

Research has shown that ocrelizumab, the treatment under study in this trial, effectively treats multiple sclerosis (MS). Over 5.5 years, studies found that patients experienced significantly fewer relapses, with a risk reduction of up to 70%. Long-term data indicates that more than three-quarters of patients with relapsing MS (RMS) remained stable without major disability progression for ten years. In primary progressive MS (PPMS), ocrelizumab slowed the disease's worsening. Other studies have confirmed these benefits, consistently showing fewer relapses and slower disease progression.678910

Who Is on the Research Team?

CT

Clinical Trials

Principal Investigator

Hoffmann-La Roche

Are You a Good Fit for This Trial?

This trial is for people with relapsing or primary progressive multiple sclerosis who are currently on an approved anti-CD20 therapy and are switching to a new form of ocrelizumab given under the skin. Participants must meet certain health requirements set by the study.

Inclusion Criteria

I have previously received CD20 antibody treatments like ofatumumab, ublituximab, or ocrelizumab.
I have been diagnosed with RMS or PPMS based on the 2017 McDonald criteria.
My EDSS disability score is between 0 and 6.5.
See 1 more

Exclusion Criteria

Participants with contraindication to Gd+ or inability to tolerate MRI procedure
Positive hepatitis B virus (HBV) and hepatitis C virus (HCV) antibody test at screening
I have a neurologic disorder that makes diagnosing RMS or PPMS difficult.
See 10 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive ocrelizumab subcutaneously at Day 1 and Week 24

48 weeks
2 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Ocrelizumab

Trial Overview

The study tests how safe, effective, and satisfactory it is to give ocrelizumab as a shot under the skin (with rHuPH20) in MS patients who switch from other similar treatments. It looks at patient outcomes, safety, and satisfaction.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: OCR SCExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Genentech, Inc.

Lead Sponsor

Trials
1,578
Recruited
569,000+
Ashley Magargee profile image

Ashley Magargee

Genentech, Inc.

Chief Executive Officer since 2024

MBA from Harvard University, BA from Princeton University

Levi Garraway profile image

Levi Garraway

Genentech, Inc.

Chief Medical Officer since 2021

MD, PhD

Citations

Ocrelizumab as first-line therapy in highly active relapsing- ...

As a first-line treatment of highly active RRMS, ocrelizumab demonstrated significant efficacy and very good tolerability.

Five-year efficacy outcomes of ocrelizumab in relapsing ... - PMC

Over 5.5 years, patients treated with OCR showed a statistically significant reduction in the risk of relapse (hazard ratios [HRs] .30 to .54) ...

Efficacy | OCREVUS® (ocrelizumab)

OCREVUS reduced the risk of disability progression in 3 endpoints across 2 identical RMS trials · Risk reduction · Risk reduction · Disability data through 10+ ...

10 Years of Ocrelizumab Treatment in Multiple Sclerosis

After 10 years, over three-quarters (76.6%) of pwRMS on OCR-OCR were free from 48W-CDP-EDSS events and 91.9% did not need a walking aid.

Genentech presents new six-year Ocrevus (Ocrelizumab) ...

ed a 42% reduction. These results suggest earlier treatment with Ocrevus reduced the risk of disability progression and this effect was sustained over time.

Safety of Ocrelizumab in Patients With Relapsing and Primary ...

To report safety of ocrelizumab (OCR) up to 7 years in patients with relapsing multiple sclerosis (RMS) and primary progressive multiple sclerosis (PPMS) ...

Safety | OCREVUS® (ocrelizumab)

Well-established safety profile with 10+ years of clinical trial data1. As of November 2023, 6155 patients have received OCREVUS in the all-exposure trial ...

Safety of Ocrelizumab in Multiple Sclerosis - Dialogo Roche

†The exposure in PY during Year 7 is limited for meaningful interpretation, so these data are presented in the plots with dotted lines. MS, multiple sclerosis; ...

Safety of Ocrelizumab in Multiple Sclerosis: Updated ...

Reported rates per 100 PY (95% CI) were: Adverse events (AEs), 230.32 (228.55–232.09); infections, 71.24 (70.26–72.23); serious AEs, 7.97 (7.64–8.30); serious ...

New Ocrevus (Ocrelizumab) data demonstrate reductions ...

New safety data remain consistent with OCREVUS' favorable benefit-risk profile in both relapsing and primary progressive multiple sclerosis (PPMS). “The OCREVUS ...