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Ocrelizumab SC
Ocrelizumab SC is a monoclonal antibody that targets CD20 on B cells.
Ocrelizumab SC is a monoclonal antibody that targets CD20 on B cells. Used for Relapsing forms of multiple sclerosis, Primary progressive multiple sclerosis, Non-Hodgkin's lymphoma.
At a glance
| Generic name | Ocrelizumab SC |
|---|---|
| Also known as | RO4964913 |
| Sponsor | Hoffmann-La Roche |
| Drug class | CD20-targeting monoclonal antibody |
| Target | CD20 |
| Modality | Small molecule |
| Therapeutic area | Immunology |
| Phase | Phase 3 |
Mechanism of action
By binding to CD20, ocrelizumab SC induces direct and indirect mechanisms of action that lead to the depletion of B cells, which play a key role in the pathogenesis of multiple sclerosis and non-Hodgkin's lymphoma.
Approved indications
- Relapsing forms of multiple sclerosis
- Primary progressive multiple sclerosis
- Non-Hodgkin's lymphoma
Common side effects
- Infusion-related reactions
- Infections
- Neutropenia
- Thrombocytopenia
- Anemia
Key clinical trials
- A Study to Investigate Effects of Ocrelizumab Treatment on Neurofilament Light Chain (NfL) Levels and Participant Satisfaction in Participants With Multiple Sclerosis (MS)
- An Extension Study to Assess Impact of Multiple Sclerosis (MS) on Physical Function and Provide Continued Ocrelizumab Treatment (PHASE3)
- A Study to Assess Bioequivalence of Two Subcutaneous (SC) Formulations of Ocrelizumab in Participants With Multiple Sclerosis (MS) (PHASE2)
- Traditional Versus Early Aggressive Therapy for Multiple Sclerosis Trial (NA)
- Multiple Sclerosis Patient Experience on Kesimpta and Ocrevus Subcutaneous Formulation
- A Phase III, Non-Inferiority, Randomized, Open-Label, Parallel Group, Multicenter Study To Investigate The Pharmacokinetics, Pharmacodynamics, Safety And Radiological And Clinical Effects Of Subcutaneous Ocrelizumab Versus Intravenous Ocrelizumab In Patients With Multiple Sclerosis (PHASE3)
- A Study To Investigate The Pharmacokinetics, Safety, And Tolerability Of Subcutaneous Ocrelizumab Administration In Participants With Multiple Sclerosis (PHASE1)
- Randomized Autologous heMatopoietic Stem Cell Transplantation Versus Alemtuzumab, Cladribine or Ocrelizumab for RRMS (RAM-MS) (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |