TheraRadar

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Data updated: Mar 10, 2026

OCREVUS ZUNOVO

OCRELIZUMAB AND HYALURONIDASE-OCSQ CD20-directed Antibody Interactions
Neurology Approved 2024-09-13

OCREVUS ZUNOVO is a combination of ocrelizumab and hyaluronidase-ocsq indicated for the treatment of multiple sclerosis in adult patients. It is approved for relapsing forms of the disease, which include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease. The medication is also indicated for the treatment of primary progressive multiple sclerosis. This therapeutic provides a CD20-directed treatment option for various stages of the condition.

Source: FDA Label • Roche • Endoglycosidase

How OCREVUS ZUNOVO Works

Ocrelizumab is a cytolytic antibody that targets CD20, an antigen found on the surface of pre-B and mature B lymphocytes. Upon binding, it induces B cell depletion through antibody-dependent cellular cytolysis and complement-mediated lysis. The hyaluronidase component functions by depolymerizing hyaluronan to transiently increase the permeability of the subcutaneous tissue at the injection site. This local effect is reversible, with tissue permeability typically restored within 24 to 48 hours.

Source: FDA Label
1
Indication
--
Phase 3 Trials
1
Years on Market

Details

Status
Prescription
First Approved
2024-09-13
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

OCREVUS ZUNOVO Approval History

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What OCREVUS ZUNOVO Treats

1 indications

OCREVUS ZUNOVO is approved for 1 conditions since its original approval in 2024. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Multiple Sclerosis
Source: FDA Label

OCREVUS ZUNOVO Target & Pathway

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Target

CD20 (B-Lymphocyte Antigen CD20) Cell Surface Marker

A protein found on the surface of B-cells but not stem cells or plasma cells. Anti-CD20 antibodies deplete B-cells, making them effective in B-cell cancers and autoimmune diseases where B-cells drive pathology.

OCREVUS ZUNOVO Competitors

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10 other drugs also target CD20. Compare mechanisms, indications, and trial activity.

View all 10 CD20 drugs →
Drug = Competitor name Company = Manufacturer N indic. = FDA-approved indications → Date = Patent/exclusivity expiry

Competitors share the same molecular target (CD20). Earlier expiry dates signal biosimilar/generic opportunities.

Drugs Similar to OCREVUS ZUNOVO

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

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OZOBAX DS
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Shared indications:
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RYANODEX
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Shared indications:
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

OCREVUS ZUNOVO FDA Label Details

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Indications & Usage

FDA Label (PDF)

OCREVUS ZUNOVO is indicated for the treatment of: Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults Primary progressive MS, in adults OCREVUS ZUNOVO is a CD20-directed cytolytic antibody indicated for the treatment of: Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults Primary progressive MS, in adults

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.