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Rituximab and Hyaluronidase Human

National Cancer Institute (NCI) · Phase 3 active Biologic

Rituximab and Hyaluronidase Human is a Monoclonal antibody with recombinant human hyaluronidase Biologic drug developed by National Cancer Institute (NCI). It is currently in Phase 3 development for B-cell non-Hodgkin lymphoma, Chronic lymphocytic leukemia, Rheumatoid arthritis. Also known as: Rituxan Hycela, Rituximab Plus Hyaluronidase, Rituximab/Hyaluronidase, Rituximab/Hyaluronidase Human.

Rituximab targets CD20 on B cells to deplete them, while hyaluronidase enables subcutaneous delivery by breaking down hyaluronic acid in subcutaneous tissue.

Rituximab targets CD20 on B cells to deplete them, while hyaluronidase enables subcutaneous delivery by breaking down hyaluronic acid in subcutaneous tissue. Used for B-cell non-Hodgkin lymphoma, Chronic lymphocytic leukemia, Rheumatoid arthritis.

At a glance

Generic nameRituximab and Hyaluronidase Human
Also known asRituxan Hycela, Rituximab Plus Hyaluronidase, Rituximab/Hyaluronidase, Rituximab/Hyaluronidase Human, Rituxan Hycela,
SponsorNational Cancer Institute (NCI)
Drug classMonoclonal antibody with recombinant human hyaluronidase
TargetCD20
ModalityBiologic
Therapeutic areaOncology, Immunology
PhasePhase 3

Mechanism of action

Rituximab is a chimeric monoclonal antibody that binds CD20 antigen on B lymphocytes, leading to B-cell depletion through antibody-dependent cellular cytotoxicity and direct apoptosis. The addition of human hyaluronidase allows for subcutaneous administration instead of intravenous infusion, improving patient convenience and potentially reducing infusion-related reactions.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Rituximab and Hyaluronidase Human

What is Rituximab and Hyaluronidase Human?

Rituximab and Hyaluronidase Human is a Monoclonal antibody with recombinant human hyaluronidase drug developed by National Cancer Institute (NCI), indicated for B-cell non-Hodgkin lymphoma, Chronic lymphocytic leukemia, Rheumatoid arthritis.

How does Rituximab and Hyaluronidase Human work?

Rituximab targets CD20 on B cells to deplete them, while hyaluronidase enables subcutaneous delivery by breaking down hyaluronic acid in subcutaneous tissue.

What is Rituximab and Hyaluronidase Human used for?

Rituximab and Hyaluronidase Human is indicated for B-cell non-Hodgkin lymphoma, Chronic lymphocytic leukemia, Rheumatoid arthritis.

Who makes Rituximab and Hyaluronidase Human?

Rituximab and Hyaluronidase Human is developed by National Cancer Institute (NCI) (see full National Cancer Institute (NCI) pipeline at /company/national-cancer-institute-nci).

Is Rituximab and Hyaluronidase Human also known as anything else?

Rituximab and Hyaluronidase Human is also known as Rituxan Hycela, Rituximab Plus Hyaluronidase, Rituximab/Hyaluronidase, Rituximab/Hyaluronidase Human, Rituxan Hycela,.

What drug class is Rituximab and Hyaluronidase Human in?

Rituximab and Hyaluronidase Human belongs to the Monoclonal antibody with recombinant human hyaluronidase class. See all Monoclonal antibody with recombinant human hyaluronidase drugs at /class/monoclonal-antibody-with-recombinant-human-hyaluronidase.

What development phase is Rituximab and Hyaluronidase Human in?

Rituximab and Hyaluronidase Human is in Phase 3.

What are the side effects of Rituximab and Hyaluronidase Human?

Common side effects of Rituximab and Hyaluronidase Human include Infusion-related reactions, Infection, Cytopenias, Fatigue, Injection site reactions.

What does Rituximab and Hyaluronidase Human target?

Rituximab and Hyaluronidase Human targets CD20 and is a Monoclonal antibody with recombinant human hyaluronidase.

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