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RITUXIMAB Drug Record

  • Summary
  • Interactions
  • Claims
  • RITUXIMAB chembl:CHEMBL1201576 ApprovedAntineoplasticImmunotherapy

    Alternate Names:

    HS006
    IDEC-102
    SAIT-101
    MABTHERA RITUXAN
    R-105 IDEC-102
    ABP-798
    CT-P10
    MABTHERA
    RITUXAN
    RG-105
    HS-006
    RHCACD20MA
    SAIT101
    HS-006 (RITUXIMAB BIOSIMILAR)
    RITUXIMAB
    IDEC-C2B8
    ANTICD20
    IG GAMMA-1 CHAIN C REGION
    drugbank:00073
    chembl:CHEMBL1201576
    rxcui:121191
    chemidplus:174722-31-7

    Drug Info:

    FDA Approval approved
    Drug Class monoclonal antibody
    Drug Indications antineoplastic agent
    Drug Class antineoplastic agents
    Year of Approval 1997
    FDA Approval Non-Hodgkin’s lymphoma, Chronic lymphocytic leukemia, Rheumatoid arthritis, Granulomatosis with polyangiitis
    Drug Class Therapeutic Antibodies
    (5 More Sources)

    Publications:

    Jaglowski et al., 2010, Rituximab in chronic lymphocytic leukemia., Semin. Hematol.
    Chen et al., 2002, TTD: Therapeutic Target Database., Nucleic Acids Res.
    van Meerten et al., 2010, CD20-targeted therapy: the next generation of antibodies., Semin. Hematol.
    McLaughlin P et al., 1998, Rituximab chimeric anti-CD20 monoclonal antibody therapy for relapsed indolent lymphoma: half of patients respond to a four-dose treatment program., J Clin Oncol
    Epeldegui M et al., 2016, Predictive Value of Cytokines and Immune Activation Biomarkers in AIDS-Related Non-Hodgkin Lymphoma Treated with Rituximab plus Infusional EPOCH (AMC-034 trial)., Clin Cancer Res
    Kalra S et al., 2018, Association of CYP2C19*2 and ALDH1A1*1/*2 variants with disease outcome in breast cancer patients: results of a global screening array., Eur J Clin Pharmacol
    Rossi D et al., 2009, Analysis of the host pharmacogenetic background for prediction of outcome and toxicity in diffuse large B-cell lymphoma treated with R-CHOP21., Leukemia
    Ghetie et al., Rituximab but not other anti-CD20 antibodies reverses multidrug resistance in 2 B lymphoma cell lines, blocks the activity of P-glycoprotein (P-gp), and induces P-gp to translocate out of lipid rafts., J. Immunother.
    Jordheim LP et al., 2015, Single nucleotide polymorphisms in ABCB1 and CBR1 can predict toxicity to R-CHOP type regimens in patients with diffuse non-Hodgkin lymphoma., Haematologica
    Márquez A et al., 2013, IL2/IL21 region polymorphism influences response to rituximab in systemic lupus erythematosus patients., Mol Biol Rep
    Butrym A et al., 2016, Dual role of the CXCL12 polymorphism in patients with chronic lymphocytic leukemia., HLA
    Jiménez Morales A et al., 2019, FCGR2A/FCGR3A Gene Polymorphisms and Clinical Variables as Predictors of Response to Tocilizumab and Rituximab in Patients With Rheumatoid Arthritis., J Clin Pharmacol
    Hatjiharissi et al., 2007, Genetic linkage of Fc gamma RIIa and Fc gamma RIIIa and implications for their use in predicting clinical responses to CD20-directed monoclonal antibody therapy., Clin Lymphoma Myeloma
    Kim et al., 2006, FCGR3A gene polymorphisms may correlate with response to frontline R-CHOP therapy for diffuse large B-cell lymphoma., Blood
    Kim SH et al., 2015, Treatment Outcomes With Rituximab in 100 Patients With Neuromyelitis Optica: Influence of FCGR3A Polymorphisms on the Therapeutic Response to Rituximab., JAMA Neurol
    Quartuccio L et al., 2014, The 158VV Fcgamma receptor 3A genotype is associated with response to rituximab in rheumatoid arthritis: results of an Italian multicentre study., Ann Rheum Dis
    Nishio M et al., 2009, FCGR3A-158V/F polymorphism may correlate with the levels of immunoglobulin in patients with non-Hodgkin's lymphoma after rituximab treatment as an adjuvant to autologous stem cell transplantation., Eur J Haematol
    Weng WK et al., 2003, Two immunoglobulin G fragment C receptor polymorphisms independently predict response to rituximab in patients with follicular lymphoma., J Clin Oncol
    Niwa et al., 2004, Enhancement of the antibody-dependent cellular cytotoxicity of low-fucose IgG1 Is independent of FcgammaRIIIa functional polymorphism., Clin. Cancer Res.
    Daïen CI et al., 2012, TGF beta1 polymorphisms are candidate predictors of the clinical response to rituximab in rheumatoid arthritis., Joint Bone Spine
    Alas et al., 2002, Rituximab modifies the cisplatin-mitochondrial signaling pathway, resulting in apoptosis in cisplatin-resistant non-Hodgkin's lymphoma., Clin. Cancer Res.
    Morimoto et al., 2005, Use of rituximab to treat refractory Diamond-Blackfan anemia., Eur. J. Haematol.
  • RITUXIMAB   CXCL13

    Interaction Score: 8.83

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    26384320


    Sources:
    PharmGKB

  • RITUXIMAB   MS4A1

    Interaction Score: 2.7

    Interaction Types & Directionality:
    antibody (inhibitory)
    inhibitor (inhibitory)

    Interaction Info:
    Mechanism of Interaction B-lymphocyte antigen CD20 inhibitor
    Direct Interaction yes
    Trial Name Rituxan

    PMIDs:
    20350663 11752352 20350667 9704735


    Sources:
    MyCancerGenome TdgClinicalTrial ChemblInteractions TEND PharmGKB TTD FDA

  • RITUXIMAB   FCGR2A

    Interaction Score: 2.52

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    30457672 17324336 16609067


    Sources:
    PharmGKB

  • RITUXIMAB   LOH19CR1

    Interaction Score: 1.77

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    15813920


    Sources:
    NCI

  • RITUXIMAB   FCGR3A

    Interaction Score: 1.66

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    30457672 26167726 23505228 19018870 16609067 12975461 17324336 15448014


    Sources:
    PharmGKB

  • RITUXIMAB   GSTA1

    Interaction Score: 1.47

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    29938344 19448608


    Sources:
    PharmGKB

  • RITUXIMAB   CXCL12

    Interaction Score: 1.26

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    27173875


    Sources:
    PharmGKB

  • RITUXIMAB   IL10

    Interaction Score: 0.52

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    26384320


    Sources:
    PharmGKB

  • RITUXIMAB   XIAP

    Interaction Score: 0.44

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    11895917


    Sources:
    NCI

  • RITUXIMAB   IL6

    Interaction Score: 0.35

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    26384320


    Sources:
    PharmGKB

  • RITUXIMAB   IL2

    Interaction Score: 0.28

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    23645042


    Sources:
    PharmGKB

  • RITUXIMAB   TGFB1

    Interaction Score: 0.24

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    22129793


    Sources:
    PharmGKB

  • RITUXIMAB   ABCB1

    Interaction Score: 0.07

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    16971809 25637052


    Sources:
    NCI PharmGKB

  • RITUXIMAB   TP53

    Interaction Score: 0.02

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    11895917


    Sources:
    NCI

  • TEND: RITUXIMAB

    • Version: 01-August-2011

    Alternate Names:
    RITUXIMAB Primary Drug Name

    Drug Info:
    Year of Approval 1997
    Drug Class antineoplastic agents

    Publications:

  • MyCancerGenome: RITUXIMAB

    • Version: 20-Jun-2017

    Alternate Names:
    IDEC-102 Development Name
    IDEC-C2B8 Development Name
    RITUXIMAB Generic Name

    Drug Info:
    Drug Class Therapeutic Antibodies
    FDA Approval Non-Hodgkin’s lymphoma, Chronic lymphocytic leukemia, Rheumatoid arthritis, Granulomatosis with polyangiitis

    Publications:

  • TdgClinicalTrial: RITUXIMAB

    • Version: January-2014

    Alternate Names:

    Drug Info:
    Drug Indications antineoplastic agent
    Drug Class monoclonal antibody
    FDA Approval approved

    Publications:

  • NCI: RITUXIMAB

    • Version: 14-September-2017

    Alternate Names:
    C1702 NCI drug code

    Drug Info:

    Publications:
    Alas et al., 2002, Rituximab modifies the cisplatin-mitochondrial signaling pathway, resulting in apoptosis in cisplatin-resistant non-Hodgkin's lymphoma., Clin. Cancer Res.
    Ghetie et al., Rituximab but not other anti-CD20 antibodies reverses multidrug resistance in 2 B lymphoma cell lines, blocks the activity of P-glycoprotein (P-gp), and induces P-gp to translocate out of lipid rafts., J. Immunother.
    Morimoto et al., 2005, Use of rituximab to treat refractory Diamond-Blackfan anemia., Eur. J. Haematol.

  • PharmGKB: rituximab

    • Version: 18-August-2020

    Alternate Names:

    Drug Info:

    Publications:
    Epeldegui M et al., 2016, Predictive Value of Cytokines and Immune Activation Biomarkers in AIDS-Related Non-Hodgkin Lymphoma Treated with Rituximab plus Infusional EPOCH (AMC-034 trial)., Clin Cancer Res
    Jordheim LP et al., 2015, Single nucleotide polymorphisms in ABCB1 and CBR1 can predict toxicity to R-CHOP type regimens in patients with diffuse non-Hodgkin lymphoma., Haematologica
    Kalra S et al., 2018, Association of CYP2C19*2 and ALDH1A1*1/*2 variants with disease outcome in breast cancer patients: results of a global screening array., Eur J Clin Pharmacol

  • TTD: Rituximab

    • Version: 2020.06.01

    Alternate Names:
    D09EXD TTD Drug ID

    Drug Info:

    Publications:

  • ChemblDrugs: chembl:CHEMBL1201576

    • Version: ChEMBL_27

    Alternate Names:

    Drug Info:

    Publications:

  • ChemblInteractions: CHEMBL1201576

    • Version: chembl_23

    Alternate Names:

    Drug Info:

    Publications:

  • FDA: Rituximab

    • Version: 04-September-2020

    Alternate Names:

    Drug Info:

    Publications:

Disclaimer: This resource is intended for purely research purposes. It should not be used for emergencies or medical or professional advice.

A finding of a drug-gene interaction or potentially druggable category does not necessarily indicate effectiveness (or lack thereof) of any drug or treatment regimen. A finding of no interaction or no potentially druggable category does not necessarily indicate lack of effectiveness of any drug or treatment regimen. Drug-gene interactions or potentially druggable categories are not presented in ranked order of potential or predicted efficacy.

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DGIdb (v4.2.0 - sha1 afd9f30b) • Last updated 2020-10-21