Subcutaneous Ocrelizumab for Multiple Sclerosis

(OCARINA 3 Trial)

Not currently recruiting at 11 trial locations
RS
Overseen ByReference Study ID Number: WN45319 https://forpatients.roche.com/
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
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 medication for multiple sclerosis (MS), to evaluate its safety and how the body processes it. The trial consists of two phases: one tests different doses, and the other administers a selected dose over time. Individuals with primary progressive or relapsing MS who have not used similar treatments in the past two years may qualify. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, providing participants the opportunity to be among the first to experience this new approach.

Is there any evidence suggesting that this treatment is likely to be safe for humans?

Research has shown that the under-the-skin (subcutaneous) form of ocrelizumab is generally well-tolerated by people with multiple sclerosis. In one study, only 2.6% of patients who received the injection experienced serious side effects, indicating that most do not have severe reactions. The safety of this subcutaneous form is similar to the IV (intravenous) form that doctors have used for some time, suggesting it is likely just as safe. Another study found no safety issues, even when antibodies to a protein called rHuPH20, which aids absorption, were present. Overall, the treatment appears safe for people with multiple sclerosis.12345

Why do researchers think this study treatment might be promising for MS?

Unlike the standard of care for multiple sclerosis, which typically involves intravenous infusions, ocrelizumab co-formulated with rHuPH20 is delivered subcutaneously. This delivery method is less invasive and can be more convenient for patients, potentially improving adherence to treatment. Researchers are excited about this approach because it combines ocrelizumab, a proven therapy for multiple sclerosis, with recombinant human hyaluronidase (rHuPH20), which enhances the absorption and distribution of the medication. This could lead to more efficient treatment with fewer side effects.

What evidence suggests that this treatment might be an effective treatment for MS?

Research has shown that subcutaneous ocrelizumab, which participants in this trial will receive, effectively treats multiple sclerosis (MS). Studies indicate that this form of ocrelizumab can almost completely prevent the return of symptoms and the development of brain lesions in MS patients. It also slows the worsening of disability in people with relapsing MS, helping them maintain their physical abilities longer. Additionally, subcutaneous injections of ocrelizumab are as effective as the intravenous (IV) form in managing brain lesions seen on MRI scans. Overall, patients report high satisfaction with the treatment, and it is well-tolerated with no major safety concerns.14567

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 diagnosed with multiple sclerosis (MS). Participants should generally be in stable health. Those with certain other medical conditions or who are unable to safely participate, as determined by the study team, will not be eligible.

Inclusion Criteria

I have been diagnosed with PPMS or RMS based on the 2017 McDonald criteria.
My EDSS disability score is between 0 and 6.5.

Exclusion Criteria

Immunocompromised state
Sensitivity or intolerance to any ingredient including excipients of ocrelizumab
Positive screening tests for active, latent, or inadequately treated hepatitis B
See 13 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Dose-escalation

Participants receive single ascending doses of ocrelizumab SC during the initial dose-escalation phase

24 weeks
1 visit (in-person) on Day 1

Dose-continuation

Participants continue treatment with the selected dose of ocrelizumab SC every 24 weeks

144 weeks
1 visit (in-person) every 24 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Ocrelizumab Co-formulated With rHuPH20

Trial Overview

The study is testing a new under-the-skin (subcutaneous) version of ocrelizumab, given alone or at increasing doses first and then continued at a selected dose. The main goal is to see if this new form is safe and well-tolerated in people with MS.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Ocrelizumab SCExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Hoffmann-La Roche

Lead Sponsor

Trials
2,482
Recruited
1,107,000+
Headquarters
Basel, Switzerland
Known For
Precision medicine
Top Products
Avastin, Herceptin, Rituxan, Accu-Chek
Dr. Levi Garraway profile image

Dr. Levi Garraway

Hoffmann-La Roche

Chief Medical Officer since 2019

MD from the University of Basel

Dr. Thomas Schinecker profile image

Dr. Thomas Schinecker

Hoffmann-La Roche

Chief Executive Officer since 2023

PhD in Molecular Biology from New York University

Citations

Subcutaneous Ocrelizumab in Patients With Multiple Sclerosis

This study provides Class II evidence that a single SC injection of 920 mg of OCR achieves a noninferior 12-week area under serum concentration– ...

Subcutaneous Ocrelizumab Well Tolerated in Patients With ...

Subcutaneous ocrelizumab (SC OCR) was found to be safe for patients with relapsing and primary progressive multiple sclerosis (RMS/PPMS).

OCREVUS ZUNOVO® (ocrelizumab & hyaluronidase-ocsq)

Learn about efficacy outcomes in OCREVUS ZUNOVO® (ocrelizumab and hyaluronidase-ocsq) clinical trials. See full safety for more information.

Subcutaneous ocrelizumab in multiple sclerosis: Results of ...

No safety concerns were observed in patients with antibodies to rHuPH20. Patients reported high levels of satisfaction with OCR SC, indicating ...

Roche's subcutaneous OCREVUS one-year data ...

Roche's subcutaneous OCREVUS one-year data demonstrates near-complete suppression of clinical relapses and brain lesions in patients with ...

Study Details | NCT05232825 | A Phase III, Non-Inferiority, ...

This study will evaluate the pharmacokinetics, pharmacodynamics, safety, immunogenicity, and radiological and clinical effects of subcutaneous (SC) ...

Ocrelizumab Subcutaneous Administration

OCR SC resulted in near-complete suppression of relapse activity up to W48; 97.2% (OCR SC/SC) vs 98.1% (OCR IV/SC) of patients were relapse-free ...