Rituximab
Established medicineAlso known as Riabni, Rituxan, Rituxan Hycela, Ruxience+1 more
Riabni, Rituxan, Rituxan Hycela, Ruxience, Truxima.
Recent clinical, regulatory, research and industry developments relating to this drug.
Effects of different B-cell-depleting strategies on the lymphatic tissue.
CD19-CAR T-cell therapy induces deep tissue depletion of B cells.
Polatuzumab Vedotin in Previously Untreated Diffuse Large B-Cell Lymphoma.
Ibrutinib-Rituximab or Chemoimmunotherapy for Chronic Lymphocytic Leukemia.
Profile
Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.
Regulatory timeline
The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.
Indication: MabThera is indicated in adults for the following indications: Non Hodgkin’s lymphoma (NHL) MabThera is indicated for the treatment of previously untreated adult patients with… Show full indicationShow less
MabThera is indicated in adults for the following indications: Non Hodgkin’s lymphoma (NHL) MabThera is indicated for the treatment of previously untreated adult patients with stage III?IV follicular lymphoma in combination with chemotherapy. MabThera maintenance therapy is indicated for the treatment of adult follicular lymphoma patients responding to induction therapy. MabThera monotherapy is indicated for treatment of adult patients with stage III?IV follicular lymphoma who are chemoresistant or are in their second or subsequent relapse after chemotherapy. MabThera is indicated for the treatment of adult patients with CD20 positive diffuse large B cell non?Hodgkin’s lymphoma in combination with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisolone) chemotherapy. MabThera in combination with chemotherapy is indicated for the treatment of paediatric patients (aged ? 6 months to < 18 years old) with previously untreated advanced stage CD20 positive diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma (BL)/Burkitt leukaemia (mature B-cell acute leukaemia) (BAL) or Burkitt-like lymphoma (BLL). Chronic lymphocytic leukaemia (CLL) MabThera in combination with chemotherapy is indicated for the treatment of patients with previously untreated and relapsed/refractory CLL. Only limited data are available on efficacy and safety for patients previously treated with monoclonal antibodies including MabThera or patients refractory to previous MabThera plus chemotherapy. Rheumatoid arthritis MabThera in combination with methotrexate is indicated for the treatment of adult patients with severe active rheumatoid arthritis who have had an inadequate response or intolerance to other disease?modifying anti?rheumatic drugs (DMARD) including one or more tumour necrosis factor (TNF) inhibitor therapies. MabThera has been shown to reduce the rate of progression of joint damage as measured by X?ray and to improve physical function, when given in combination with methotrexate. Granulomatosis with polyangiitis and microscopic polyangiitis MabThera, in combination with glucocorticoids, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (Wegener’s) (GPA) and microscopic polyangiitis (MPA). MabThera, in combination with glucocorticoids, is indicated for the induction of remission in paediatric patients (aged ? 2 to < 18 years old) with severe, active GPA (Wegener’s) and MPA. Pemphigus vulgaris MabThera is indicated for the treatment of patients with moderate to severe pemphigus vulgaris (PV).
Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.
Research activity
Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.
Major research themes8
Journals, researchers & institutions
- The New England journal of medicine3
- Annals of the rheumatic diseases2
- Blood1
- Clinical and experimental immunology1
- Journal of neurology, neurosurgery, and psychiatry1
- Nature reviews. Disease primers1
- Auth J2
- Bergmann C2
- Bozec A2
- Bucci L2
- Burke JM2
- Corte G2
- Eckstein M2
- Grieshaber-Bouyer R2
- Institute of Pathology and Comprehensive Cancer Center EMN2
- Boston Medical Center and Boston University School of Medicine1
- Brain and Mind Centre1
- Centre for Kidney Research1
- Centre for Rheumatology1
- Centre Henri-Becquerel and University of Rouen1
Related diseases
Regulator-approved indications and conditions co-mentioned with this drug across the research literature. Number shows shared papers.
Related drugs
Drugs sharing diseases, protein targets and literature with this one. Ranked by graph evidence (shared targets + diseases weighted above co-mentions).
Studied across 14 of the same disease areas as Rituximab in the shared literature.
Studied across 10 of the same disease areas as Rituximab in the shared literature.
Studied across 9 of the same disease areas as Rituximab in the shared literature.
Studied across 9 of the same disease areas as Rituximab in the shared literature.
Studied across 8 of the same disease areas as Rituximab in the shared literature.
Studied across 5 of the same disease areas as Rituximab in the shared literature.
Studied across 3 of the same disease areas as Rituximab in the shared literature.
Studied across 3 of the same disease areas as Rituximab in the shared literature.
- RxNorm (U.S. National Library of Medicine) — drug identity
- Europe PMC — research literature
- Regulatory event sources are credited in the Regulatory Timeline above.