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Rituximab

Generic Name
Rituximab
Brand Names
MabThera, Riabni, Rituxan, Rituxan Hycela, Ruxience, Truxima, Blitzima, Rixathon, Riximyo
Drug Type
Biotech
CAS Number
174722-31-7
Unique Ingredient Identifier
4F4X42SYQ6

Overview

Rituximab is a genetically engineered chimeric murine/human monoclonal antibody directed against the CD20 antigen found on the surface of normal and malignant B lymphocytes. The antibody is an IgG1 kappa immunoglobulin containing murine light and heavy-chain variable region sequences and human constant region sequences , . It was originally approved by the U.S. FDA in 1997 as a single agent to treat patients with B-cell Non-Hodgkin's Lymphoma (NHL) , however, has now been approved for a variety of conditions . On November 28, 2018, the US FDA approved Truxima, the first biosimilar to Rituxan (Rituximab) .

Background

Rituximab is a genetically engineered chimeric murine/human monoclonal antibody directed against the CD20 antigen found on the surface of normal and malignant B lymphocytes. The antibody is an IgG1 kappa immunoglobulin containing murine light and heavy-chain variable region sequences and human constant region sequences , . It was originally approved by the U.S. FDA in 1997 as a single agent to treat patients with B-cell Non-Hodgkin's Lymphoma (NHL) , however, has now been approved for a variety of conditions . On November 28, 2018, the US FDA approved Truxima, the first biosimilar to Rituxan (Rituximab) .

Indication

Rituximab is indicated for the treatment of adult patients with relapsed or refractory, low-grade or follicular, CD20-positive, B-cell non-Hodgkin’s Lymphoma (NHL) as a single agent. Also, it is indicated for the treatment of adult patients with previously untreated follicular, CD20-positive, B-cell NHL in combination with first line chemotherapy and, in patients achieving a complete or partial response to a rituximab product in combination with chemotherapy, as single-agent maintenance therapy. Additionally, rituximab is indicated for the treatment of adult patients with non-progressing (including stable disease), low-grade, CD20-positive, B-cell NHL as a single agent after first-line cyclophosphamide, vincristine, and prednisone (CVP) chemotherapy; and previously untreated diffuse large B-cell, CD20-positive NHL in combination with cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) or other anthracycline-based chemotherapy regimens. Rituximab, in combination with fludarabine and cyclophosphamide (FC), is indicated for the treatment of adult patients with previously untreated and previously treated CD20-positive chronic lymphocytic leukemia (CLL). In combination with methotrexate, rituximab is indicated for the treatment of adult patients with moderately-to severely-active rheumatoid arthritis who have had an inadequate response to one or more TNF antagonist therapies. Additionally, rituximab, in combination with glucocorticoids, is indicated for the treatment of adult and pediatric patients 2 years of age and older with Granulomatosis with Polyangiitis (GPA) (Wegener’s Granulomatosis) and Microscopic Polyangiitis (MPA). RITUXAN (rituximab injection for intravenous use) is indicated for the treatment of pediatric patients aged 6 months and older with previously untreated, advanced stage, CD20-positive diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma (BL), Burkitt-like lymphoma (BLL) or mature B-cell acute leukemia (B-AL) in combination with chemotherapy; as well as the treatment of adult patients with moderate to severe pemphigus vulgaris. These indications for RITUXAN are not included in the labels of rituximab biosimilar products (rituximab-arrx, rituximab-abbs, rituximab-pvvr). The combination product RITUXAN HYCELA (rituximab and hyaluronidase human injection, for subcutaneous use) is not indicated for the treatment of non-malignant conditions.

Associated Conditions

  • Active, Moderate to Severe Rheumatoid Arthritis
  • Chronic Lymphocytic Leukemia
  • Diffuse Large B-Cell Lymphoma (DLBCL)
  • Follicular Non-Hodgkin's Lymphoma
  • Granulomatosis With Polyangiitis
  • Microscopic Polyangiitis (MPA)
  • Advanced Burkitt Lymphoma (BL)
  • Advanced Burkitt-like lymphoma
  • Advanced Diffuse Large B-Cell Lymphoma (DLBCL)
  • Advanced Mature B-cell type acute leukaemia
  • Moderate Pemphigus Vulgaris (PV)
  • Non-progressive Low Grade Non-Hodgkin's Lymphoma (NHL)
  • Refractory Low Grade Non-Hodgkin's Lymphoma (NHL)
  • Refractory follicular B-cell non-Hodgkin's lymphoma
  • Relapsed Low Grade Non-Hodgkin's Lymphoma (NHL)
  • Relapsed follicular B-cell non-Hodgkin's lymphoma
  • Severe Pemphigus Vulgaris (PV)

FDA Approved Products

Riabni
Manufacturer:Amgen Inc
Route:INTRAVENOUS
Strength:500 mg in 50 mL
Approved: 2023/02/28
NDC:55513-326
Rituxan
Manufacturer:Genentech, Inc.
Route:INTRAVENOUS
Strength:10 mg in 1 mL
Approved: 2023/06/06
NDC:50242-051
Riabni
Manufacturer:Amgen Inc
Route:INTRAVENOUS
Strength:100 mg in 10 mL
Approved: 2023/02/28
NDC:55513-224
Rituxan Hycela
Manufacturer:Genentech, Inc.
Route:SUBCUTANEOUS
Strength:120 mg in 1 mL
Approved: 2022/11/16
NDC:50242-109
Truxima
Manufacturer:Cephalon, Inc.
Route:INTRAVENOUS
Strength:10 mg in 1 mL
Approved: 2022/11/02
NDC:63459-103

Singapore Approved Products

RIXATHON CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML
Manufacturer:Lek Pharmaceuticals d.d. (Ljubljana)
Form:INFUSION, SOLUTION CONCENTRATE
Strength:100mg/10ml
Online:Yes
Approved: 2020/06/30
Approval:SIN15970P
MABTHERA CONCENTRATE FOR SOLUTION FOR INFUSION 500 mg/50ml
Manufacturer:GENENTECH INC, Roche Diagnostics GmbH, Genentech, Inc (Hillsboro)
Form:INJECTION
Strength:10 mg/ml
Online:Yes
Approved: 1998/08/22
Approval:SIN09946P
RIXATHON CONCENTRATE FOR SOLUTION FOR INFUSION 500MG/50ML
Manufacturer:Lek Pharmaceuticals d.d. (Ljubljana)
Form:INFUSION, SOLUTION CONCENTRATE
Strength:500mg/50ml
Online:Yes
Approved: 2020/06/30
Approval:SIN15969P

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