Rituximab
Monoclonal antibody targets MS4A1
Regulatory milestones approvals, filings & regulatory actions · 21 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansions (15) | US (FDA) | RITUXAN | — | 2006-02-10 – 2021-12-02 | fda.gov ↗ |
| Label expansions (2) | US (FDA) | RUXIENCE | — | 2020-05-26 – 2021-11-15 | fda.gov ↗ |
| Label expansions (2) | US (FDA) | TRUXIMA | — | 2019-05-23 – 2019-12-18 | fda.gov ↗ |
| Approved | EU (EMA) | MabThera | — | 1998-06-02 | europa.eu ↗ |
| Approved | US (FDA) | RITUXAN | — | 1997-11-26 | fda.gov ↗ |
Trials 1,444 · started per year
Also used as a comparator or background therapy in 890 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 010 trials | ||||||
| Phase 0 | NCT07519005 Background | Jan → Feb 2026 overdue | liver failure | Xijing Hospital | Active not recruiting | No outcome recorded |
| Phase 0 | NCT04161248 Background | Sep 2020 → Dec 2026 expected | B-cell non-Hodgkin lymphoma | Canadian Cancer Trials Group | Active not recruiting | No outcome recorded |
| Phase 0 | NCT03684980 Background | Nov 2018 → Nov 2027 expected | central nervous system non-hodgkin lymphoma | Memorial Sloan Kettering Cancer Center | Active not recruiting | No outcome recorded |
| Phase 0 | NCT03295240 Background | Sep 2017 → Jan 2024 | mantle cell lymphoma | Memorial Sloan Kettering Cancer Center | Completed | No outcome recorded |
| Phase 0 | NCT01760226 Background | Jan 2013 → Aug 2016 | post-transplant lymphoproliferative disease, primary mediastinal large B-cell lymphoma | Baylor College of Medicine | Completed | No outcome recorded |
| Phase 0 | NCT01184885 Background | Jul 2010 → Mar 2011 | Burkitt lymphoma, acute lymphoblastic leukemia, adult T-cell leukemia/lymphoma, lymphoblastic lymphoma +1 | Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University | Completed | No outcome recorded |
| Phase 0 | NCT01022021 Comparator | Jan 2010 → Apr 2014 | lymphoma | University of Kansas Medical Center | Completed | No outcome recorded |
| Phase 0 | NCT00736450 Background | Jul 2008 → Oct 2012 | diffuse large B-cell lymphoma | University of Nebraska | Terminated | No outcome recorded |
| Phase 0 | NCT00515138 Background | May 2007 → Nov 2011 | B-cell non-Hodgkin lymphoma | University of California, San Francisco | Terminated | No outcome recorded |
| Phase 0 | NCT00790413 Background | Aug 2005 → Dec 2022 | neuroblastoma | Lund University Hospital | Unknown | No outcome recorded |
| Phase 1144 trials | ||||||
| Phase 1 | NCT07714421 Background | Dec 2026 → Oct 2030 expected | high grade B-cell lymphoma, primary mediastinal large B-cell lymphoma | Jonsson Comprehensive Cancer Center | Not yet recruiting | No outcome recorded |
| Phase 1 | NCT07649304 Background | Sep 2026 → Apr 2028 expected | high grade B-cell lymphoma, high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement, plasmablastic lymphoma, primary effusion lymphoma | National Cancer Institute (NCI) | Not yet recruiting | No outcome recorded |
| Phase 1 | NCT07225439 Background | Sep 2026 → Dec 2027 expected | chronic lymphocytic leukemia/small lymphocytic lymphoma, follicular lymphoma, high grade B-cell lymphoma, mantle cell lymphoma +2 | Paolo Caimi, MD | Not yet recruiting | No outcome recorded |
| Phase 1 | NCT07444710 Background | Aug 2026 → Sep 2027 expected | mantle cell lymphoma | National Cancer Institute (NCI) | Not yet recruiting | No outcome recorded |
| Phase 1 | NCT07697339 Comparator | Jul 2026 → Aug 2027 expected | mantle cell lymphoma | Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd. | Not yet recruiting | No outcome recorded |
| Show all 144 trials opens the full record — a long page | ||||||
| Phase 1/2135 trials | ||||||
| Phase 1/2 | NCT07638787 Background | Jun 2026 → Sep 2027 expected | large B-cell lymphoma | Ruijin Hospital | Not yet recruiting | No outcome recorded |
| Phase 1/2 | NCT07294677 Background | Mar 2026 → Mar 2032 expected | leukemia, lymphoma | University of Chicago | Recruiting | No outcome recorded |
| Phase 1/2 | NCT07432022 Background | Mar 2026 → Jun 2028 expected | aggressive B-cell non-Hodgkin lymphoma | Shanghai EpimAb Biotherapeutics Co., Ltd. | Not yet recruiting | No outcome recorded |
| Phase 1/2 | NCT07398638 Background | Feb 2026 → Feb 2029 expected | diffuse large B-cell lymphoma | Sun Yat-sen University | Not yet recruiting | No outcome recorded |
| Phase 1/2 | NCT07222631 Background | Feb 2026 → Feb 2031 expected | cancer, non-Hodgkin lymphoma | University of California, San Diego | Recruiting | No outcome recorded |
| Show all 135 trials opens the full record — a long page | ||||||
| Phase 2320 trials | ||||||
| Phase 2 | NCT07137481 Background | Feb 2027 → Jul 2030 expected | hematopoietic and lymphoid cell neoplasm | M.D. Anderson Cancer Center | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT07654426 Background | Oct 2026 → Dec 2030 expected | chemotherapy-induced toxicity, diffuse large B-cell lymphoma | Beth Israel Deaconess Medical Center | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT07662928 Background | Sep 2026 → May 2031 expected | Burkitt lymphoma | AIDS Malignancy Consortium | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT07677813 Background | Jun 2026 → Dec 2029 expected | MCD diffuse large B-cell lymphoma | Ou Bai, MD/PHD | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT07464210 Background | Jun 2026 → Aug 2029 expected | Waldenstrom macroglobulinemia | Seoul National University Hospital | Not yet recruiting | No outcome recorded |
| Show all 320 trials opens the full record — a long page | ||||||
| Phase 2/325 trials | ||||||
| Phase 2/3 | NCT07712588 Background | Sep 2027 → Jan 2031 expected | diffuse large B-cell lymphoma | Dizal Pharmaceuticals | Not yet recruiting | No outcome recorded |
| Phase 2/3 | NCT07634471 Background | Jun 2026 → Jul 2032 expected | follicular lymphoma | Merck Sharp & Dohme LLC | Recruiting | No outcome recorded |
| Phase 2/3 | NCT07185373 Background | Oct 2025 → Sep 2028 expected | primary central nervous system lymphoma | Huashan Hospital | Not yet recruiting | No outcome recorded |
| Phase 2/3 | NCT05991388 Background | May 2024 → May 2031 expected | B-cell non-Hodgkin lymphoma | University of Birmingham | Recruiting | No outcome recorded |
| Phase 2/3 | NCT05786768 Comparator | Oct 2023 → Oct 2027 expected | idiopathic steroid-sensitive nephrotic syndrome | Assistance Publique - Hôpitaux de Paris | Recruiting | No outcome recorded |
| Phase 2/3 | NCT05553496 Comparator | Sep 2022 → Apr 2023 | — | Ain Shams University | Unknown | No outcome recorded |
| Phase 2/3 | NCT04799275 Background | May 2021 → Mar 2027 expected | T-cell/histiocyte rich large B cell lymphoma, diffuse large B-cell lymphoma activated B-cell type, diffuse large B-cell lymphoma germinal center B-cell type, diffuse large B-cell lymphoma with chronic inflammation +5 | National Cancer Institute (NCI) | Active not recruiting | No outcome recorded |
| Phase 2/3 | NCT04442022 Background | Sep 2020 → Dec 2026 expected | diffuse large B-cell lymphoma | Karyopharm Therapeutics Inc | Active not recruiting | No outcome recorded |
| Phase 2/3 | NCT04061512 Background | Feb 2020 → Mar 2030 expected | Waldenstrom macroglobulinemia | University College, London | Recruiting | No outcome recorded |
| Phase 2/3 | NCT03829566 Background | Nov 2019 → Jan 2025 | neuromyelitis optica | Northwestern University | Withdrawn | No outcome recorded |
| Phase 2/3 | NCT03984448 Background | Oct 2019 → Apr 2028 expected | high grade B-cell lymphoma, high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement | National Cancer Institute (NCI) | Active not recruiting | No outcome recorded |
| Phase 2/3 | NCT04074187 Background | Oct 2019 → May 2021 | thrombotic thrombocytopenic purpura | Sanofi | Completed | No outcome recorded |
| Phase 2/3 | NCT03366272 Background | Dec 2017 → Jan 2025 | non-Hodgkin lymphoma | Saarland University | Completed | No outcome recorded |
| Phase 2/3 | NCT02763319 Comparator | Nov 2016 → Jun 2024 | diffuse large B-cell lymphoma | Incyte Corporation | Completed | No outcome recorded |
| Phase 2/3 | NCT01805557 Background | Feb 2013 → Mar 2019 | diffuse large B-cell lymphoma | Fondazione Italiana Linfomi - ETS | Completed | No outcome recorded |
| Phase 2/3 | NCT01716442 Comparator | Aug 2012 → Sep 2013 | idiopathic steroid-sensitive nephrotic syndrome, steroid-resistant nephrotic syndrome | Seoul National University Childrens Hospital | Unknown | No outcome recorded |
| Phase 2/3 | NCT01180036 Comparator | Nov 2011 → Oct 2017 | idiopathic membranous glomerulonephritis | Mayo Clinic | Completed | No outcome recorded |
| Phase 2/3 | NCT01277172 Comparator | Oct 2010 → Sep 2011 | diffuse large B-cell lymphoma | Probiomed S.A. de C.V. | Unknown | No outcome recorded |
| Phase 2/3 | NCT01197560 Comparator | Sep 2010 → Jul 2013 | diffuse large B-cell lymphoma | Celgene Corporation | Completed | No outcome recorded |
| Phase 2/3 | NCT05063513 Comparator | Jul 2009 → Jul 2013 | systemic lupus erythematosus | European Society for Blood and Marrow Transplantation | Withdrawn | No outcome recorded |
| Phase 2/3 | NCT00565331 Comparator | Dec 2007 → Dec 2013 | — | Radboud University Medical Center | Completed | No outcome recorded |
| Phase 2/3 | NCT00096460 Comparator | Aug 2004 → Mar 2006 | follicular lymphoma | Medical College of Wisconsin | Terminated | No outcome recorded |
| Phase 2/3 | NCT00261118 Comparator | Apr 2004 → Aug 2009 | ulcerative colitis | Royal Liverpool University Hospital | Completed | No outcome recorded |
| Phase 2/3 | NCT00774202 Comparator | Nov 2003 → Feb 2008 | autoimmune thrombocytopenic purpura | Weill Medical College of Cornell University | Completed | No outcome recorded |
| Phase 2/3 | NCT00147121 Comparator | Sep 2002 → Feb 2010 | B-cell non-Hodgkin lymphoma | Haruhiko Fukuda | Completed | No outcome recorded |
| Phase 3210 trials | ||||||
| Phase 3 | NCT07220187 Background | Aug 2026 → Oct 2035 expected | Richter transformation | SWOG Cancer Research Network | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT07189325 Comparator | Jun 2026 → Jun 2031 expected | relapsing-remitting multiple sclerosis | University Hospital, Montpellier | Recruiting | No outcome recorded |
| Phase 3 | NCT07104032 Comparator | Jun 2026 → Dec 2027 expected | primary central nervous system lymphoma | Ono Pharmaceutical Co., Ltd. | Recruiting | No outcome recorded |
| Phase 3 | NCT07562022 Comparator | May 2026 → May 2028 expected | follicular lymphoma | Sinocelltech Ltd. | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT07409428 Background | Mar 2026 → Apr 2028 expected | diffuse large B-cell lymphoma | Hutchmed | Recruiting | No outcome recorded |
| Show all 210 trials opens the full record — a long page | ||||||
| Phase 423 trials | ||||||
| Phase 4 | NCT06906549 Comparator | Jul 2025 → Jul 2026 overdue | rheumatoid arthritis | University Hospital, Strasbourg, France | Recruiting | No outcome recorded |
| Phase 4 | NCT06611696 Comparator | Nov 2024 → Mar 2027 expected | anti-neutrophil cytoplasmic antibody-associated vasculitis | Chiba University | Recruiting | No outcome recorded |
| Phase 4 | NCT05514015 Comparator | Mar 2024 → Sep 2026 expected | idiopathic membranous glomerulonephritis | First Affiliated Hospital, Sun Yat-Sen University | Recruiting | No outcome recorded |
| Phase 4 | NCT05494593 Background | Feb 2023 → Aug 2025 | mucopolysaccharidosis type 2 | Takeda | Withdrawn | No outcome recorded |
| Phase 4 | NCT06134284 Background | Jan 2023 → Dec 2026 expected | marginal zone lymphoma | Lixia Sheng | Recruiting | No outcome recorded |
| Phase 4 | NCT04127747 Comparator | Aug 2020 → Dec 2022 | autoimmune disease | Second Affiliated Hospital, School of Medicine, Zhejiang University | Unknown | No outcome recorded |
| Phase 4 | NCT04134247 Background | Nov 2019 → Nov 2021 | non-Hodgkin lymphoma | Shandong Provincial Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT04083066 Background | Sep 2019 → Apr 2023 | primary central nervous system lymphoma | Mingzhi Zhang | Unknown | No outcome recorded |
| Phase 4 | NCT04152577 Background | Jun 2019 → Oct 2021 | B-cell non-Hodgkin lymphoma | Shandong Provincial Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT04033276 Comparator | Jan 2019 → Dec 2021 | — | Seoul National University Hospital | Completed | No outcome recorded |
| Phase 4 | NCT03513601 Background | Jul 2017 → May 2019 | diffuse large B-cell lymphoma | Mingzhi Zhang | Unknown | No outcome recorded |
| Phase 4 | NCT02749292 Comparator | Jun 2016 → Jan 2022 | anti-neutrophil cytoplasmic antibody-associated vasculitis | Massachusetts General Hospital | Terminated | No outcome recorded |
| Phase 4 | NCT02626845 Comparator | Dec 2015 → Jul 2017 | granulomatosis with polyangiitis | Hospital for Special Surgery, New York | Terminated | No outcome recorded |
| Phase 4 | NCT05116228 Comparator | Sep 2015 → Nov 2021 | rheumatoid arthritis | Medical University of Vienna | Terminated | No outcome recorded |
| Phase 4 | NCT02525172 Background | Aug 2015 → Jul 2020 | glycogen storage disease II | National Taiwan University Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT02526823 Comparator | Aug 2015 → Dec 2019 | lymphoma | Shandong Provincial Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT02378298 Comparator | Dec 2011 → Sep 2019 | endocrine exophthalmos | Göteborg University | Completed | No outcome recorded |
| Phase 4 | NCT01295151 Comparator | Aug 2011 → Nov 2015 | rheumatoid arthritis | Julia Brown | Completed | No outcome recorded |
| Phase 4 | NCT01312064 Comparator | Apr 2011 → Apr 2012 | impaired renal function disease | National Taiwan University Hospital | Terminated | No outcome recorded |
| Phase 4 | NCT01593332 Comparator | Jul 2010 → Sep 2011 | rheumatoid arthritis | Mashhad University of Medical Sciences | Completed | No outcome recorded |
| Phase 4 | NCT01000441 Comparator | Dec 2009 → Aug 2013 | rheumatoid arthritis | University Hospital, Strasbourg, France | Completed | No outcome recorded |
| Phase 4 | NCT00908583 Background | May 2009 → Nov 2012 | anti-HLA hyperimmunization | University of Cincinnati | Completed | No outcome recorded |
| Phase 4 | NCT00466258 Background | Oct 2006 → May 2009 | HIV infectious disease, diffuse large B-cell lymphoma | PETHEMA Foundation | Completed | No outcome recorded |
| Phase not applicable22 trials | ||||||
| — | NCT07703657 Comparator | Jul 2026 → Jul 2027 expected | Epstein-Barr virus infection, disease arising from reactivation of latent virus, disease related to hematopoietic stem cell transplant | Yang Donglin | Not yet recruiting | No outcome recorded |
| — | NCT07389356 Comparator | Feb 2026 → Oct 2027 expected | diffuse large B-cell lymphoma | The First Affiliated Hospital with Nanjing Medical University | Not yet recruiting | No outcome recorded |
| — | NCT05821192 Background | Mar → Apr 2023 | angioimmunoblastic T-cell lymphoma, peripheral T-cell lymphoma, not otherwise specified | Ou Bai, MD/PHD | Unknown | No outcome recorded |
| — | NCT05809180 Background | Jan 2023 → Jul 2025 | diffuse large B-cell lymphoma | The First Affiliated Hospital of Soochow University | Unknown | No outcome recorded |
| — | NCT05040555 Background | Aug 2021 → Sep 2023 overdue | diffuse large B-cell lymphoma | Ou Bai, MD/PHD | Recruiting | No outcome recorded |
| — | NCT04519710 Background | Sep 2020 → Sep 2021 | hepatitis B virus infection | Centre de Recherches et d'Etude sur la Pathologie Tropicale et le Sida | Completed | No outcome recorded |
| — | NCT04432402 Background | Jun 2020 → Dec 2022 | diffuse large B-cell lymphoma | The First Affiliated Hospital with Nanjing Medical University | Unknown | No outcome recorded |
| — | NCT03412188 Comparator | Aug 2018 → Sep 2021 | autoimmune thrombocytopenic purpura | Nayera Hazaa Elsherif | Completed | No outcome recorded |
| — | NCT03022123 Background | Nov 2016 → Nov 2017 | diffuse large B-cell lymphoma | Hebei Medical University Fourth Hospital | Unknown | No outcome recorded |
| — | NCT02652468 Background | Mar 2016 → Sep 2018 | lymphoma | University of Wisconsin, Madison | Completed | No outcome recorded |
| — | NCT01643928 Comparator | Aug 2012 → Mar 2016 | rheumatoid arthritis | Pfizer | Completed | No outcome recorded |
| — | NCT01843868 Background | Jan 2012 → Jun 2015 | non-Hodgkin lymphoma | Australasian Leukaemia and Lymphoma Group | Withdrawn | No outcome recorded |
| — | NCT01350232 Background | Sep 2009 → Aug 2011 | sickle cell-beta zero-thalassemia, sickle cell-hemoglobin c disease syndrome | Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University | Terminated | No outcome recorded |
| — | NCT00651755 Background | Mar 2008 → Sep 2011 | lymphoma | M.D. Anderson Cancer Center | Completed | No outcome recorded |
| — | NCT00544219 Background | Sep 2007 → Sep 2012 | lymphoma | Swiss Cancer Institute | Completed | No outcome recorded |
| — | NCT00530179 Comparator | Jul 2007 → Feb 2014 | diffuse large B-cell lymphoma | AHS Cancer Control Alberta | Completed | No outcome recorded |
| — | NCT00561379 Comparator | Apr 2005 → May 2013 | diffuse large B-cell lymphoma | Nantes University Hospital | Completed | No outcome recorded |
| — | NCT00082836 Background | Dec 2004 → May 2007 | lymphoma | Memorial Sloan Kettering Cancer Center | Completed | No outcome recorded |
| — | NCT00110006 Background | Dec 2004 → ? | lymphoma | Case Comprehensive Cancer Center | Withdrawn | No outcome recorded |
| — | NCT00695097 Comparator | Aug 2004 → Dec 2010 | acute transplant rejection | University of California, San Francisco | Completed | No outcome recorded |
| — | NCT00145587 Background | Jul 2004 → Feb 2009 | osteopetrosis | St. Jude Children's Research Hospital | Terminated | No outcome recorded |
| — | NCT00307593 Comparator | May 2004 → Jun 2007 | eosinophilic granulomatosis with polyangiitis, microscopic polyangiitis | Assistance Publique - Hôpitaux de Paris | Completed | No outcome recorded |
| Phase not stated1 trial | ||||||
| — | NCT02136511 Background | — | B-cell chronic lymphocytic leukemia | Gilead Sciences | Approved for marketing | No outcome recorded |
Press releases naming this drug 60 releases
| Date | Issuer | Release |
|---|---|---|
| 2026-07-06 | AbbVie | AbbVie Announces TEPKINLY® (epcoritamab) in Combination with Lenalidomide and Rituximab is Approved by the European Commission for the Treatment of Relapsed or Refractory Follicular Lymphoma abbvie.com ↗ |
| 2025-12-22 | Incyte Corporation | Incyte Japan Announces Approval of Minjuvi® (tafasitamab) in Combination with Rituximab and Lenalidomide for the Treatment of Relapsed or Refractory Follicular Lymphoma incyte.com ↗ |
| 2025-11-18 | AbbVie | AbbVie Announces U.S. FDA Approval of EPKINLY® (epcoritamab-bysp) in Combination with Rituximab and Lenalidomide for Relapsed or Refractory Follicular Lymphoma abbvie.com ↗ |
| 2025-06-18 | Incyte Corporation | Incyte Announces FDA Approval of Monjuvi® (tafasitamab-cxix) in Combination with Rituximab and Lenalidomide for Patients with Relapsed or Refractory Follicular Lymphoma incyte.com ↗ |
| 2022-06-06 | Amgen | FDA APPROVES RIABNI™ (RITUXIMAB-ARRX), A BIOSIMILAR TO RITUXAN® (RITUXIMAB), FOR ADULTS WITH MODERATE TO SEVERE RHEUMATOID ARTHRITIS amgen.com ↗ |
| 2021-04-19 | Incyte Corporation | Incyte and MorphoSys Announce First Patient Dosed in Phase 3 inMIND Study Evaluating the Addition of Tafasitamab to Lenalidomide and Rituximab in Relapsed or Refractory Follicular or Marginal Zone Lymphoma incyte.com ↗ |
| 2020-12-17 | Amgen | FDA Approves Amgen's RIABNI™ (rituximab-arrx), A Biosimilar To Rituxan® (rituximab) amgen.com ↗ |
| 2020-12-07 | Roche Global Development | New data presented at ASH 2020 reinforces the benefit/risk profile of fixed-duration Polivy plus bendamustine and MabThera/Rituxan in patients with relapsed or refractory diffuse large B-cell lymphoma roche.com ↗ |
| 2020-05-04 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva and Celltrion Healthcare Announce the Launch of TRUXIMA® (rituximab-abbs) Injection for Rheumatoid Arthritis, the Only Biosimilar to Rituxan® (rituximab) Available in the United States for This Indication tevapharm.com ↗ |
| 2020-04-02 | Pfizer | Pfizer Receives European Approval for Oncology Biosimilar, RUXIENCE™ (rituximab) pfizer.com ↗ |
| 2020-01-31 | Pfizer | Pfizer Receives Positive CHMP Opinion for Oncology Biosimilar, RUXIENCE™ (rituximab) pfizer.com ↗ |
| 2019-12-19 | Amgen | Amgen And Allergan Submit Biologics License Application For ABP 798, Biosimilar Candidate To Rituxan® (rituximab), To U.S. Food And Drug Administration amgen.com ↗ |
| 2019-11-08 | AbbVie | AbbVie Submits Supplemental New Drug Application to U.S. FDA For IMBRUVICA® (ibrutinib) in Combination with Rituximab for the Treatment of Previously Untreated, Younger Adults with Chronic Lymphocytic Leukemia abbvie.com ↗ |
| 2019-11-08 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva and Celltrion Announce the Availability of TRUXIMA® (rituximab-abbs) Injection, the First Biosimilar to Rituxan® (rituximab) in the United States tevapharm.com ↗ |
| 2019-10-14 | Roche Global Development | Phase III PEMPHIX study shows Roche’s MabThera/Rituxan (rituximab) superior to mycophenolate mofetil in patients with pemphigus vulgaris roche.com ↗ |
| 2019-09-30 | Roche Global Development | FDA approves Roche’s Rituxan (rituximab) in children with two rare blood vessel disorders roche.com ↗ |
| 2019-08-22 | Amgen | Amgen And Allergan Announce Positive Top-Line Results From Comparative Clinical Study Of ABP 798, Biosimilar Candidate To Rituxan® (Rituximab) amgen.com ↗ |
| 2019-07-23 | Pfizer | FDA Approves Pfizer’s Biosimilar, RUXIENCE™ (rituximab-pvvr), for Certain Cancers and Autoimmune Conditions pfizer.com ↗ |
| 2019-03-15 | Roche Global Development | European Commission approves Roche's MabThera (rituximab) for a rare autoimmune disease roche.com ↗ |
| 2019-01-24 | Amgen | Amgen And Allergan Announce Positive Top-Line Results From Phase 1/ Phase 3 Study Of ABP 798, Biosimilar Candidate To Rituximab amgen.com ↗ |
| 2018-12-04 | AbbVie | IMBRUVICA® (ibrutinib) Combination Regimen Significantly Improved Survival Versus the Chemoimmunotherapy FCR (Fludarabine, Cyclophosphamide and Rituximab) in Previously Untreated and Younger Chronic Lymphocytic Leukemia (CLL) Patients; Late-Breaking Phase 3 Data at ASH 2018 abbvie.com ↗ |
| 2018-12-02 | Pfizer | Pfizer Presents Positive 26-Week Data For PF-05280586, A Potential Biosimilar To Rituximab, At The American Society Of Hematology Annual Meeting pfizer.com ↗ |
| 2018-12-01 | AbbVie | AbbVie Presents New Data from Phase 3 MURANO Trial of VENCLEXTA®/VENCLYXTO® (venetoclax) in Combination with Rituximab in Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia Who Completed the Fixed Treatment Course abbvie.com ↗ |
| 2018-11-28 | Teva Branded Pharmaceutical Products R&D, Inc. | Celltrion and Teva Announce FDA Approval of TRUXIMA® (rituximab-abbs), a Biosimilar to RITUXAN®, for Three Non-Hodgkin’s Lymphoma Indications tevapharm.com ↗ |
| 2018-11-02 | Novartis Pharmaceuticals | Sandoz decides not to pursue US biosimilar rituximab; will focus on robust biosimilar portfolio for unmet access and sustainability needs novartis.com ↗ |
| 2018-11-01 | Roche Global Development | Roche announces EU approval of Venclyxto plus MabThera for people with previously treated chronic lymphocytic leukaemia roche.com ↗ |
| 2018-11-01 | AbbVie | AbbVie Receives European Commission Approval of VENCLYXTO® (venetoclax) Plus Rituximab for the Treatment of Patients with Chronic Lymphocytic Leukemia Who Have Received at Least One Prior Therapy abbvie.com ↗ |
| 2018-09-21 | AbbVie | AbbVie Receives Positive CHMP Opinion for a Novel, Chemotherapy-free Combination of VENCLYXTO® (venetoclax tablets) with Rituximab as a Treatment with a Fixed Duration for Patients with Chronic Lymphocytic Leukemia Who Have Received at Least One Prior Therapy abbvie.com ↗ |
| 2018-08-27 | AbbVie | AbbVie Announces IMBRUVICA® (ibrutinib) Plus Rituximab Approval by U.S. FDA as First Chemotherapy-Free Combination Treatment in Adults with Waldenström's Macroglobulinemia, a Rare Type of Blood Cancer abbvie.com ↗ |
| 2018-06-25 | AbbVie | IMBRUVICA® (ibrutinib) Supplemental New Drug Application Accepted for Review by U.S. FDA with Potential to Broaden Treatment Use as a Combination Treatment Option with Rituximab in Waldenström's Macroglobulinemia (WM), A Rare Form of Blood Cancer abbvie.com ↗ |
| 2018-06-15 | Roche Global Development | New long-term data confirm Roche's Gazyva/Gazyvaro extends the lives of people with chronic lymphocytic leukaemia compared to MabThera/Rituxan roche.com ↗ |
| 2018-06-15 | AbbVie | AbbVie Announces New Undetectable Minimal Residual Disease Data from Phase 3 Relapsed/Refractory Chronic Lymphocytic Leukemia MURANO Trial of Venetoclax in Combination with Rituximab at 23rd European Hematology Association Annual Congress abbvie.com ↗ |
| 2018-06-11 | Roche Global Development | Roche announces FDA approval for Venclexta plus Rituxan for people with previously treated chronic lymphocytic leukaemia roche.com ↗ |
| 2018-06-08 | AbbVie | AbbVie Announces U.S. FDA Approval of VENCLEXTA® (venetoclax tablets) in Combination with Rituximab as a Fixed Duration Treatment for Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma Patients Who Have Received One Prior Therapy abbvie.com ↗ |
| 2018-06-01 | AbbVie | Phase 3 IMBRUVICA® (ibrutinib) Data Suggest Improved Treatment Outcomes in Waldenström's Macroglobulinemia (WM), a Rare Form of Blood Cancer, in Combination with Rituximab versus Rituximab Alone abbvie.com ↗ |
| 2018-05-02 | Novartis Pharmaceuticals | Sandoz receives complete response letter from the US FDA for proposed biosimilar rituximab novartis.com ↗ |
| 2018-01-24 | Pfizer | Pfizer Announces Positive Top-Line Results For Potential Biosimilar To Rituxan®/MabThera® pfizer.com ↗ |
| 2017-12-12 | Roche Global Development | Roche announces phase III data showing Venclexta/Venclyxto plus MabThera/Rituxan reduced the risk of disease progression or death by 83% compared to a standard of care regimen in previously treated chronic lymphocytic leukaemia roche.com ↗ |
| 2017-12-12 | AbbVie | AbbVie Announces Phase 3 Study of VENCLEXTA™/ VENCLYXTO™ (venetoclax) in Combination with Rituxan® (rituximab) Meets its Primary Endpoint abbvie.com ↗ |
| 2017-12-10 | Roche Global Development | Phase II data showed Roche’s investigational polatuzumab vedotin plus bendamustine and MabThera/Rituxan (BR) increased complete response rates compared to BR alone in previously treated aggressive lymphoma roche.com ↗ |
| 2017-12-05 | AbbVie | IMBRUVICA® (ibrutinib) Plus Rituximab Phase 3 iNNOVATE Trial in Rare Waldenström's Macroglobulinemia Met Primary Endpoint abbvie.com ↗ |
| 2017-09-18 | Roche Global Development | Phase III data showed that Venclexta/Venclyxto plus MabThera/Rituxan helped people with previously treated chronic lymphocytic leukaemia live longer without their disease worsening compared to bendamustine plus MabThera/Rituxan roche.com ↗ |
| 2017-09-18 | AbbVie | AbbVie Announces Positive Topline Results from Phase 3 Trial Evaluating VENCLEXTA™/VENCLYXTO™ (Venetoclax) Tablets in Combination with Rituxan® (rituximab) for the Treatment of Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia abbvie.com ↗ |
| 2017-09-12 | Novartis Pharmaceuticals | Sandoz proposed biosimilar rituximab accepted for review by the FDA novartis.com ↗ |
| 2017-06-29 | Teva Branded Pharmaceutical Products R&D, Inc. | Celltrion and Teva Announce U.S. FDA Acceptance of Biologics License Application for Proposed Biosimilar to Rituxan® (rituximab) tevapharm.com ↗ |
| 2017-06-23 | Roche Global Development | FDA approves Rituxan Hycela (rituximab and hyaluronidase human) for subcutaneous injection in certain blood cancers roche.com ↗ |
| 2017-06-19 | Novartis Pharmaceuticals | Sandoz receives approval in Europe for Rixathon® (biosimilar rituximab) to treat blood cancers and immunological diseases novartis.com ↗ |
| 2017-04-21 | Novartis Pharmaceuticals | Sandoz proposed biosimilars rituximab and etanercept recommended for approval in Europe* novartis.com ↗ |
| 2016-12-05 | Roche Global Development | Roche’s Gazyva/Gazyvaro Helped People With Previously Untreated Follicular Lymphoma Live Significantly Longer Without Their Disease Worsening Compared to MabThera/Rituxan roche.com ↗ |
| 2016-12-05 | Novartis Pharmaceuticals | New interim data demonstrate Sandoz proposed biosimilar rituximab has equivalent efficacy to reference product novartis.com ↗ |
| 2016-06-09 | Novartis Pharmaceuticals | New data demonstrates Sandoz' etanercept and rituximab biosimilar candidates bioequivalent to originator products novartis.com ↗ |
| 2016-05-31 | Roche Global Development | Roche's subcutaneous formulation of MabThera receives approval in Europe for people with chronic lymphocytic leukaemia roche.com ↗ |
| 2016-05-27 | Roche Global Development | Roche’s Gazyva/Gazyvaro showed superior progression-free survival compared to MabThera/Rituxan in people with previously untreated follicular lymphoma roche.com ↗ |
| 2016-05-24 | Novartis Pharmaceuticals | Sandoz' biosimilar rituximab regulatory submission accepted by European Medicines Agency novartis.com ↗ |
| 2016-01-20 | AbbVie | AbbVie's Venetoclax Receives Breakthrough Therapy Designation from FDA in Combination with Rituximab for the Treatment of Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia abbvie.com ↗ |
| 2015-12-08 | Gilead Sciences | Phase 3 Results for Zydelig® With Bendamustine and Rituximab for Relapsed Chronic Lymphocytic Leukemia (CLL) Presented at American Society of Hematology Annual Meeting gilead.com ↗ |
| 2015-11-16 | Gilead Sciences | Gilead’s Zydelig® Combined with Bendamustine and Rituximab Shows Superior Efficacy to Bendamustine/Rituximab in Phase 3 Study of Patients with Relapsed Chronic Lymphocytic Leukemia gilead.com ↗ |
| 2015-06-17 | AbbVie | ImmunoGen's IMGN529 for B-Cell Malignancies Demonstrates Synergistic Activity with Rituximab in Preclinical Models of Non-Hodgkin Lymphoma abbvie.com ↗ |
| 2015-06-12 | AbbVie | Phase 1b Study of Investigational Treatment Venetoclax with Rituximab Shows Clinical Response in Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia abbvie.com ↗ |
| 2013-12-09 | AbbVie | ImmunoGen, Inc. Announces Activity Reported with SAR3419 Plus Rituxan In Difficult-to-Treat Patient Population abbvie.com ↗ |
Evidence & citations 52 cited values
Every value below carries the sentence it was read from. 2,360 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | rituximab | “Patients initially received one 21-day cycle of standard rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP; rituximab 375 mg/m2, cyclophosphamide...” PMID 30948276 ↗ Apr 20192288“All enrolled patients will first complete a total of 6-8 cycles (21 days per cycle) of Standard R-CHOP chemotherapy (Rituximab + Cyclophosphamide + Doxorubicin + Prednisolone)...” NCT05874778 ↗ “A Phase 3 Open Label Multicenter, Randomized Study to Compare the Efficacy and Safety of the Zevalin (Ibritumomab Tiuxetan) Therapeutic Regimen Following Cyclophosphamide,...” NCT00384111 ↗ “Assess the CR and ORR following treatment with VELCADE (bortezomib), Nipent (pentostatin) and Rituxan (rituximab) (VNR) in subjects with follicular lymphoma (FL), marginal zone...” NCT01460602 ↗ “This study evaluates the addition of Acalabrutinib to current standard therapy of Rituximab, Cyclophosphamide, Doxorubicin, Vincristine and Prednisolone (R-CHOP) for patients...” NCT04546620 ↗ “The purpose of the study is to assess the efficacy of the association of Lenalidomide (Revlimid) and R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, vincristine and...” NCT01393756 ↗ “All patients will receive 8 cycles of R-CHOEP immunochemotherapy every two weeks with the following doses per cycle: rituximab 375 mg/m², cyclophosphamide 750 mg/m²,...” NCT03399513 ↗ “R-IDARAM comprised of rituximab 375 mg/m2 (day 1), idarubicin 10 mg/m2(day 2 and 3); dexamethasone 100 mg/m2 (12 h.infusion in day 2, 3 and 4); cytarabine 1 g/m2 (1 h. infusion...” NCT02657785 ↗ “Intrathecal administration of 2nd, 3rd, and 4th doses of methotrexate 15 mg and hydrocortisone 50mg on day 2 or 3 of 2nd, 3rd, and 4th cycles of immunochemotherapy with...” NCT03123718 ↗ “rituximab and modified hyperfractionated cyclophosphamide, vincristine doxorubicin, dexamethasone (hyperCVAD) administered every 28 days for 4-6 cycles followed by rituximab...” NCT00581854 ↗ “Four cycles of Induction therapy: Rituximab 375mg/m2 d1; Methotrexate 3.5g/m2 d2;Temozolomide 100mg/m2 d2-6; for patients who reach a CR, PR, or SD, will proceed to autologous...” NCT02399189 ↗ “R-IDARAM comprised of rituximab 375 mg/m2 (day 1), idarubicin 10 mg/m2(day 2); dexamethasone 100 mg/m2 (12 h.infusion in day 2, 3 and 4); cytarabine 1 g/m2 (1 h. infusion in...” NCT02836158 ↗ “zanubrutinib combined with Pola-R-CHP regimen: zanubrutinib 160mg bid d1-d21/C1-C6; polatuzumab 1.8mg/kg d1/C1-C6; rituximab 375mg/㎡, iv, d1/C1-C6; cyclophosphamide 750mg/㎡,...” NCT07371923 ↗ “This is a phase 1/2 open label study to assess the safety and efficacy of pixantrone in combination with bendamustine, etoposide and , for CD20 positive B-cell lymphomas,...” NCT02678299 ↗ “A Randomized, Double-blind, Parallel-arm, Phase I Study to Evaluate the Pharmacokinetics and Pharmacodynamics of BI 695500 vs. Rituximab (MabThera) Induction Immunotherapy as a...” NCT01950273 ↗ “standard doses of R-CHOP21 chemotherapy (375 mg/m(2) intravenous rituximab, 750 mg/m(2) intravenous cyclophosphamide, 50 mg/m(2) intravenous doxorubicin, and 1·4 mg/m(2)...” PMID 24831981 ↗ May 2014 “At present, the only treatment option is Rituximab (an anti-cluster of differentiation antigen 20 (CD20) monoclonal antibody), which effectuates a limited but clinically...” NCT05939037 ↗ “Eligible patients received intravenous rituximab 375 mg/m2, cyclophosphamide 750 mg/m2, doxorubicin 50 mg/m2, and vincristine 1·4 mg/m2 (maximum 2 mg/m2), and oral prednisone...” PMID 34022150 ↗ May 2021 “A Phase 1, Multi-center, Open-label, Uncontrolled, Dose-escalation Trial to Evaluate the Safety of OPB-111077 in Combination With Bendamustine and Rituximab in Patients With...” NCT04049825 ↗ “Prior to or within 2 weeks after initiation of TPO-RAs therapy, a single dose of Rituximab at 375mg/m2 or divided doses of Rituximab at 100mg once a week for 2-4 weeks, or a...” NCT04915482 ↗ “Evaluation of the efficacy, tolerance, quality of life and cost effectiveness of the association of Oxaliplatin, Gemcitabine, Rituximab and Dexamethasone for treatment of...” NCT01019863 ↗ “PL-doxorubicin 35-40 mg/m(2) and epirubicin 70 mg/m(2) were given in combination with standard dosage of prednisone, vincristine, cyclophosphamide, rituximab (according to...” NCT03022123 ↗ “OBJECTIVE To test whether Rituximab (RTX) is efficacious to achieve complete renal response (CR) in Lupus Nephritis (LN) patients with persistent proteinuria (≥1g/d) despite at...” NCT01673295 ↗ “The purpose of the study is to determine the recommended dose (RD) of lenalidomide (Revlimid) when administered in association with R-CHOP (rituximab (R), cyclophosphamide,...” NCT00901615 ↗ “Torisel in association with Rituximab-Cyclophosphamide-Doxorubicin-Vincristine-Prednisone (R-CHOP) administered every 3 weeks (21 days) for 6 cycles for patients in...” NCT01389427 ↗ “short-course chemoimmunotherapy with cyclophosphamide, doxorubicin, vincristine, prednisone, and rituximab (CHOP-R) followed by 90-Y ibritumomab tiuxetan (RIT) with extended...” PMID 18981007 ↗ Nov 2008 “Study on the Treatment of Double/Triple-hit Diffuse Large B-cell Lymphoma With Chidamide and Lisaftoclax in Combination With Vepesidil, Rituximab, Cyclophosphamide, Adriamycin,...” NCT07552324 ↗ “Treatment with [90Y]-ibritumomab tiuxetan is preceded by an infusion of rituximab (Rituxan, Mabthera) in order to optimize the biodistribution of radiolabeled antibody by...” NCT00850512 ↗ “Cyclophosphamide (800 mg/m2 IV over 1 hour)+ vincristine (1.5 mg/m2 IV PUSH)+ doxorubicin (40 mg/m2 IV)+ high-dose methotrexate (2,700 mg/m2 IV over 23 hours)+ rituximab (500...” NCT00392990 ↗ “R-HCVAD - Rituximab (375 mg/m2), Cyclophosphamide (300 mg/m2), Mesna (600 mg/m2), Doxorubicin (50 mg/m2), Vincristine (2 mg total), Dexamethasone (40 mg total), Methotrexate...” NCT01854372 ↗ “Group one (control group) received R-CHOP standard chemotherapy {Rituximab, Cyclophosphamide, Hydroxyldaunorubicin (Doxorubicin)®, Vincristine (oncovin)®, prednisolone in the...” PMID 33394214 ↗ Jan 2021 “Patients with a persistently positive interim-PET scan assigned to arm B1 will receive another six cycles of the (R-)CHOP regimen (rituximab, cyclophosphamide, doxorubicine,...” NCT00554164 ↗ “GP2013, a biosimilar rituximab, and innovator rituximab (RTX) in patients with rheumatoid arthritis (RA) with inadequate response or intolerance to tumour necrosis factor...” PMID 28637670 ↗ Jun 2017 “By sequentially combining Rituximab and Abatacept, we thus aim to enhance the tolerogenic potential of these drugs and seek to eliminate autoantibody production and...” NCT04120831 ↗ “with varied cycles, including Daunorubicin, Vincristine, Prednisone, Pegaspargase, Rituximab, Cytarabine, Mercaptopurine, Cyclophosphamide, Methotrexate, Doxorubicin,...” NCT04845035 ↗ “Switching to a non-TNFi-biologic (choice from non-TNFi-biologics; currently available are rituximab, abatacept, tocilizumab, or sarilumab) in people with active RA despite...” NCT04692493 ↗ “All applications of 90Y-Ibritumomab-Tiuxetan will be preceded by rituximab infusions at a dose of 250 mg/m2 at days -21 and day -14 (DL1) or day -12 (DL2) or day -10 (DL3-5),...” NCT00521560 ↗ “Day 1 of each cycle will consist of an infusion of rituximab followed by the initiation of a 96-hour continuous infusion of etoposide, doxorubicin, and vincristine and oral prednisone.” NCT00799136 ↗ “Rituximab 375 mg/m2 d0; Lenalidomide 25mg/d d1-10; Ifosfamide 5g/m2 d2; Carboplatin calculate according to AUC=5 (single dose ≤800 mg); Etoposide 100mg/m2 d1-3; Tirelizumab 200mg d6.” NCT05050630 ↗ “Etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (EPOCH-R) followed by idiotype vaccine and granulocyte-macrophage colony-stimulating factor (GM-CSF).” NCT00005780 ↗ “Participants who experience life-threatening toxicities caused by uncontrollable proliferation of fhB7H3.CAR-Ts will receive infusion of Rituximab (Rituxan or Ruxience or Halpryza)” NCT05211557 ↗ “ZR2:Rituximab 375mg/m2, D1, Lenalidomide 24mg qd D1-14, zebutinib 160mg bid RDHAP:Rituximab 375mg/m2 D0, dexamethasone 40mg D1-4, cytarabine 2g/m2 q12h D2, cisplatin 25mg/m2 D1-3.” NCT05992597 ↗ “Patients received 375 mg/m(2) rituximab, 400 mg/m(2) cyclophosphamide, 25 mg/m(2) doxorubicin, and 1 mg vincristine on day 1 of each cycle, and 40 mg/m(2) prednisone on days 1-5.” PMID 21482186 ↗ Apr 2011 “This multi-center clinical study will evaluate the efficacy of Rituximab maintenance treatment of newly diagnosed follicular lymphoma after induction therapy of BR, RCHOP or R2.” NCT04842318 ↗ “Approximately four weeks after the completion of the last cyclophosphamide dose, patients will receive rituximab 375mg/m2 as an intravenous infusion once weekly for four doses.” NCT00003659 ↗ “Rituximab 375 mg/m2, Cyclophosphamide 750 mg/m2, Doxorubicin 50 mg/m2 and Vincristine 1.4 mg/m2 (maximum total 2 mg) administered by IV infusion on Day 1 of each 21-day cycle.” NCT05189197 ↗ “Temozolomide, Etoposide, Doxil, Dexamethasone, Ibrutinib, and Rituximab (TEDDI-R) in Aggressive B-cell Lymphomas With Secondary Involvement of the Central Nervous System (CNS)” NCT03964090 ↗ “R2: Drug: Rituximab 2 doses of Rituximab (375 mg/m²) before the start of the first chemotherapy cycle, 2 doses of Rituximab before the start of the second chemotherapy cycle” NCT05518383 ↗ “Rituximab 375mg/m2 at day 0, Meththylprednisolone 500mg IV at days 1 to 5, Etoposide 40mg/m2 at days 1 to 4, Cisplatin 25mg/m2 at days 1 to 4, Cytarabine 2000mg/m2 at day 5.” NCT01278602 ↗ “Drug: Rituximab Rituximab:Participants with previously untreated DLBCL will receive rituximab at a dose of 375 mg/m\^2 IV on Day 1 of Cycle 1-8, during induction treatment.” NCT04023916 ↗ “Rituximab, an anti-CD20 monoclonal antibody, and prednisone, a glucocorticoid, further enhance anti-lymphoma activity and are established components of immunochemotherapy.” NCT07159906 ↗ “Subsequent to durvalumab infusion, rituximab was administered by IV. Rituximab administration could be split over 2 consecutive days according to local clinical practice.” NCT03003520 ↗ “azacitidine S.C 25 mg/m2 D1,2,3,4,5 rituximab I.V. 375 mg/m2 D8 gemcitabine I.V. 1,000 mg/m2, D8,15 dexamethasone I.V. or P.O. 40 mg D8,9,10,11 cisplatin 70 mg/m2 I.V. D8” NCT03719989 ↗ “This is a phase II (2 parts), open-label, single arm, multicenter study to evaluate the efficacy and safety of nemtabrutinib in combination with bortezomib and rituximab” NCT07464210 ↗ “Patients will receive in addition to ciclosporine A and corticosteroids (prednisone) 1 mg/kg/day, Rituximab at 375 mg/m²/infusion once a week for 4 consecutive weeks.” NCT01135641 ↗ “Rituximab 375mg/m2 D1; cyclophosphamide 750mg/m2 D2; adriamycin 50 mg/m2 D2 vincristine 1.4mg/m(Max 2mg) D2; prednisone 100mg/d D2-6; Zanubrutinib 160 mg, bid D1-21” NCT06005870 ↗ “Rituximab 375mg/ m2 IV day 1 Cyclophosphamide 750mg/ m2 IV day 1 Adriamycin 50mg/ m2 IV day 1 Vincristine 1.4mg/ m2 (max 2mg) IV day 1 Prednisone 100mg po days 1-5” NCT00530179 ↗ “we evaluated safety and efficacy of minimal residual disease (MRD)-driven venetoclax, lenalidomide, and rituximab (venetoclax-R2) in relapsed/refractory (R/R) MCL” PMID 38113470 ↗ Jan 2024 “Intravenous administration: Rituximab 375 mg/m2, Cyclophosphamide 400 mg/m2, Doxorubicin 25 mg/m2, Vincristine 1 mg, and Oral administration: Prednisone 40 mg/m2” NCT07215585 ↗ “sequential intravenous administration of Rituximab, Cyclophosphamide (specifically dose-adjusted for end-stage renal disease), and rabbit Thymoglobulin (rATG)” NCT07607197 ↗ “Preclinical data demonstrate enhanced antitumor effect when lumiliximab, an anti-CD23 monoclonal antibody, is combined with fludarabine or rituximab.” PMID 19843887 ↗ Oct 2009 “This phase 1b study evaluated safety and efficacy of acalabrutinib, venetoclax, and rituximab (AVR) in treatment-naive mantle cell lymphoma (TN MCL).” PMID 38781315 ↗ Sep 2024 “Brentuximab Vedotin, 1.8mg/kg/dose, d0、Rituximab, 375 mg/m2, d0、Cyclophosphamide, 750 mg/m2, d1、Doxorubicin, 50 mg/m2, d1、Prednisone, 60mg/m2, d1-5” NCT06925555 ↗ “The desensitization regimen consisted of 2 doses of IVIG (2 g/kg), a single dose of rituximab (375 mg/m), and 4 doses of bortezomib (1.3 mg/m).” PMID 26844479 ↗ Feb 2016 “Rituximab will be administered within 24 hours of the infusion in an effort to prevent post transplantation lymphoproliferative disorders (PTLPD).” NCT00145587 ↗ “Dose Adjusted - Etoposide Prednisone Vincristine Cyclophosphamide Doxorubicin - Rituximab (DA-EPOCH-R) and nivolumab are both feasible treatments.” NCT03620578 ↗ “In this research study, the investigators are adding the drug rituximab (Rituxan) to the drug cytarabine for the stem cell mobilization process.” NCT01182415 ↗ “Glofitamab plus gemcitabine and oxaliplatin (GemOx) versus rituximab-GemOx for relapsed or refractory diffuse large B-cell lymphoma (STARGLO)” PMID 39550172 ↗ Nov 2024 “Induction (2 cycles): Vincristine, Prednis(ol)one, Methotrexate, Leucovorin, Cyclophosphamide, Doxorubicin, IT medications, G-CSF, Rituximab” NCT01046825 ↗ “1 bag containing 1000 mg of rituximab* in 500 ml of NaCl 0.9% * Mabthera® and all registered biosimilars are likely to be used in this trial” NCT05211401 ↗ “Rituximab: 375 mg/m2, endovenous, according to the protocol of the service, day 1 (except in the first cycle, in which it will be on day 5).” NCT01066429 ↗ “Nivolumab 40 mg (Day 2), Rituximab 375 mg/m2 (Day 1) and Prednisolone 60 mg/m2 (Days 1-5) are administered at constant unchangeable doses.” NCT06871007 ↗ “polatuzumab vedotin x1; dexamethasone x 5; vincristine x1, cyclophosphamide x 3; doxorubicin x1; methotrexate x; rituximab 2x; ITT x1” NCT05253495 ↗ “R: (Rituximab): Day 1 50 mg/m2, Day 3 325 mg/m2, for the first week, then single doses of 500 mg/m2 every four weeks, for 21 weeks” NCT00391066 ↗ “R: (Rituximab): Day 1 50 mg/m2, Day 3 325 mg/m2, for the first week, then single doses of 500 mg/m2 every four weeks, for 21 weeks” NCT00801060 ↗ “A) Rituximab 375 mg/sqm on day 1 every 90 days for 8 cycles B) Lenalidomide (10 mg daily on days 1-21 every 28 days) for 24 cycles” NCT02390869 ↗ “3 Cycles(1 Cycle:4weeks) of Rituximab Plus CHOP (Cyclophosphamide, Adriamycin, Vincristine, and Prednisolone) Immunochemotherapy” NCT03399747 ↗ “Rituximab is a so-called direct-targeting mAb, which binds to the CD20 molecule on the surface of normal and malignant B cells.” NCT03307746 ↗ “R-GemOx regimen includes Rituximab Injection, Gemcitabine Hydrochloride for Injection, Gemcitabine Hydrochloride for Injection.” NCT06601504 ↗ “Rituximab is a genetically engineered chimeric murine/human monoclonal IgG1 kappa antibody directed against the CD20 antigen.” NCT06334991 ↗ “either Rituximab 375mg/m², intravenous infusion, Day 1 of each cycle, C1-C6; or Obinutuzumab 1000mg, intravenous infusion” NCT07355699 ↗ “During Zevalin treatment, rituximab 250 mg/m2 will be administered with the same methods mentioned above on days 1 and 8” NCT01157988 ↗ “At least 1 hour after motexafin gadolinium administration, patients receive rituximab IV over 3-4 hours on days 1 and 8.” NCT00089284 ↗ “Cyclophosphamide 750 mg/m2, pixantrone 150 mg/m2, vincristine 1.4 mg/m2, rituximab 375 mg.m2 on Day 1 of a 21 day cycle” NCT00268853 ↗ “Impact of Rituximab (RTx) Induction and Living Donation on Immunoregulation and Virus Control in Renal Transplantation” NCT01136395 ↗ “R-CHOP is a combination regimen consisting of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone.” NCT04661007 ↗ “Rituximab: 375 mg/mq day 1 Ciclofosfamide: 750 mg/mq day 1, Vincristina: 1,4 mg/mq day 1 Prednisone: 40 mg/mq day 1-5,” NCT00774826 ↗ “rituximab 375 mg/m2 on day 1 in addition to bendamustine 90 mg/m2 intravenously over 30-60 minutes on days 1 and 2” NCT00864942 ↗ “D1 : Rituximab 375 mg/m² IV + Cyclophosphamide 750 mg/m² IV + Doxorubicin 50 mg/m² IV + Vincristine 1.4 mg/m² IV.” NCT03931642 ↗ “3 cycles of lenalidomide 5mg, etoposide, methylprednisolone, cisplatin, cytarabine and rituximab every 3 weeks.” NCT02340936 ↗ “Polatuzumab Vedotin in Combination With Zanubrutinib, Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone” NCT07608978 ↗ “First-line Treatment of PCNSL With the Combination of Orelabrutinib, Rituximab, and Methotrexate (ORM Regimen)” NCT06454266 ↗ “Rituximab 375 mg/m2 IV 0 day, Dexamethasone 10 mg/m2/day IV 1 - 5 days, Methotrexate 1000 mg/m2 12 h IV 1 day” NCT02842931 ↗ “Pola-R-CHP is a combination of rituximab, cyclophosphamide, doxorubicin, prednisone, and polatuzumab vedotin” NCT06743945 ↗ “80 mg of AT-101 once daily for three days every other week, 375 mg/m2 of rituximab weekly for up to 12 weeks” NCT00286780 ↗ “* tocilizumab * rituximab * HSCT from the haploidentical donor, ex vivo depleted of alpha/beta T lymphocytes” NCT04000698 ↗ “Two kinds of anti-CD 20 monoclonal antibody could be used in this study, including Rituximab and Ortuzumab.” NCT05718856 ↗ “Doses of iv rituximab (1 g) were given on d 1 and 15, after pretreatment with 125 mg iv methylprednisolone.” PMID 22767640 ↗ Jul 2012 “dose-adjusted etoposide, doxorubicin, cyclophosphamide, vincristine, prednisone, and rituximab (DA-EPOCH-R)” PMID 32453640 ↗ May 2020 “Efficacy and Safety of Rituximab in Reducing Relapses in Children With Steroid-Sensitive Nephrotic Syndrome” NCT07049172 ↗ “Rituximab: One gm i.v. will be administered on day 6 and day 15 after completion of the TPE on those days.” NCT03286556 ↗ “Rituximab, HD-MTX, HD-Ara C, Cyclophosphamide, Iphosphamide, Vincristin, Vindesin, Temozolomide, Depocyte” NCT01458730 ↗ “Rituximab and other anti-CD20 according to the respective site's standard procedure for desensitization.” NCT04935177 ↗ “Rituximab will be administered intravenously at 375 mg/m2 at Day -13 and 1000 mg/m2 at Days -6, +1, +8.” NCT01208896 ↗ “The antibody Rituximab was administered within 24 hours of the infusion in an effort to prevent PTLPD.” NCT00143559 ↗ “Rituximab (Mabthera®) will be given as 1000mg at weeks 0 and 2, and then repeated at weeks 24 and 26.” NCT01638715 ↗ “Investigators choice single agent - Chlorambucil, Rituximab, Cytarabine, Gemcitabine, or Fludarabine” NCT00875667 ↗ “Patients with active RA were randomly assigned to rituximab (1,000 mg on days 1 and 15) or placebo.” PMID 18512710 ↗ Jun 2008 “Cyclophosphamide (Cy) + Doxorubicin (ADM) + Vincristine (VDS) + Prednisone (Pred) ]± Rituximab (R)” NCT06520163 ↗ “treatment with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP)” NCT00466258 ↗ “Rituximab (if given) will be 375 mg/m2 on Days 3 and 13 of Cycle A and on Days 4 and 9 of cycle B” NCT01184885 ↗ “Rituxan (Rituximab) Treatment in Patients With CD20+, B-Cell Follicular Non-Hodgkin's Lymphoma.” NCT00251394 ↗ “Drug: Rituximab Rituximab will be given at a dose of 375 mg/m2 by IV on day 1 in a 21-day cycle” NCT06890585 ↗ “Efficacy and Safety of Rituximab in the Treatment of Anti-Vimentin Antibody-associated Diseases” NCT07051070 ↗ “Rituximab will be administered as an IV infusion at the standard dose of 375 mg/m2 for 4 doses” NCT00774202 ↗ “Treatment included eight doses of rituximab and four doses of intrathecal liposomal cytarabine” PMID 26282634 ↗ Aug 2015 “Methylprednisolone, Equine ATG, Cyclosporine, Fludarabine, Melphalan, Thiotepa and Rituximab.” NCT00582816 ↗ “Rituximab will be administered on day 1 of courses 1-6 at 375 mg/m2 concurrently with CHOP-R.” NCT01527422 ↗ “Acalabrutinib, lenalidomide, rituximab will be given as described in the "Arms" decriptions.” NCT04094142 ↗ “R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (or prednisolone))” NCT02054559 ↗ “Etoposide, Prednisone, Doxorubicin, Cyclophosphamide, Vincristine, Rituximab, Pegfilgrastim” NCT02142049 ↗ “Zevalin study treatment regimen consisted of 2 rituximab i.v. infusions (Day 1 and Day 7-9)” NCT00322218 ↗ “Rituximab was administered within 24 hours of the transplant in an effort to prevent PTLPD.” NCT00145613 ↗ “SHR-A1912 combined with R-Chemo: SHR-A1912 + R-Chemo (Rituximab + Chemotherapy) (Phase 1b)” NCT06104553 ↗ “Rituximab: A monoclonal antibody that binds to the CD20 antigen on the surface of B cells.” NCT06829771 ↗ “Chidamide Plus R-CHOP (Rituximab、Cyclophosphamide、Doxorubicin、Vincristine and Prednisone)” NCT06891157 ↗ “Rituximab (375mg/m\^2) on day 1, every 3 weeks, only used in patients with CD20+ lymphoma” NCT05299164 ↗ “either rituximab + gemcitabine + oxaliplatin [R-GemOx], or bendamustine + rituximab [BR]” NCT04628494 ↗ “Patients with negative CSF-ctDNA results will continue with one more cycle of Rituximab.” NCT06594432 ↗ “either rituximab + gemcitabine + oxaliplatin [R-GemOx], or bendamustine + rituximab [BR]” NCT07226752 ↗ “The R-CHOP include rituximab, cyclophosphamide, doxorubicin, vincristine, and prednison.” NCT05234684 ↗ “some patients will respond to treatment with the chimeric anti-CD 20 antibody Rituximab” NCT01134432 ↗ “CD20mab is recommened as Rituximab as per the protocol, other CD20mab is also allowed.” NCT06463691 ↗ “In the R-CHOP50 group, patients were given rituximab 375 mg/m2 intravenously on day 0” PMID 31126528 ↗ Jun 2019 “patients received 375 mg/m2 of Rituximab once every 4 weeks by intravenous injection” NCT07505849 ↗ “Proposed rituximab biosimilar, 100mg or 500mg, concentrate for solution for infusion” NCT04268771 ↗ “Rituximab 375 mg/m2 intravenously (IV) starting on Day 8, Cycle 1 of lenalidomide.” NCT00765245 ↗ “Rituximab will be given by intravenous infusion for 1 day out of each 28 day cycle” NCT00868413 ↗ “Prevention of EBV reactivation Rituximab 150mg/m2 intravenously at Day+5 post HSCT” NCT06646497 ↗ “Lymphoma Protocol consisting of four weekly doses of 375 mg/m2 of rituximab (RTX)” NCT06680349 ↗ “Rituximab, Gemcitabine, Oxaliplatin, Polatuzumab vedotin, Bendamustine, Rituximab” NCT04844866 ↗ “NB02 (Poseltinib) combined with Rituximab and lenalidomide as a Salvage Therapy” NCT06737250 ↗ “R-CHOP (Rituximab, Cyclophosphamide, doxorubicin, vincristine, and prednisone)” NCT00582725 ↗ “Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP)” NCT05051891 ↗ “Rituximab 375 mg/m2 iv, day 1, cycle 1. 1400 mg s c OR 375 mg/m2 iv cycles 2-6” NCT04332822 ↗ “Rituximab is designed to attach to cancer cells, which may cause them to die.” NCT01983761 ↗ “R-CHOP (Rituximab , Cyclophosphamide ,Doxorubicine ,Vincristine , Prednisone)” NCT02858258 ↗ “rituximab, cyclophosphamide, doxorubicin, etoposide, vincristine, prednisone” NCT03293173 ↗ “Chlorambucil orally administered and Rituximab via IV infusion for 6 cycles.” NCT04578613 ↗ “* rituximab (R): 375 mg/m² IV D1 cycle 1 and 500 mg/m² IV D1 cycles 2 to 6.” NCT04010968 ↗ “Lenalidomide 25mg once daily for 21 days and rituximab 375mg/m2 for 7 days” NCT05014100 ↗ “antibody administration (Siplizumab (or ATGAM), rituximab and tegoprubart)” NCT06972069 ↗ “Patients obtain the standard of care: combination rituximab and venetoclax” NCT05069051 ↗ “R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine,prednisone)” NCT03023878 ↗ “fludarabine/cyclophosphamide/rituximab (FCR), bendamustine/rituximab (BR)” NCT03836261 ↗ “Rituximab: 375mg/m2, d6; Gemcitabine: 1g/m2, d7 Oxaliplatin: 100mg/m2, d7” NCT06778902 ↗ “Rituximab (Mabthera/Rituxan®) will be administered as per local practice” NCT04833114 ↗ “Rituximab 100mg per vial 375mg/m2, intravenous drip, Day 1 of each cycle” NCT07072208 ↗ “Introduction treatment: Rituximab, lenalidomide, chidamide for 2 cycles:” NCT06674096 ↗ “Efficiency and Tolerance of Rituximab (mabthéra) in Bullous Pemphigoid” NCT00525616 ↗ “rituximab, 375 mg per square meter of body-surface area days -7 and -2” NCT00063817 ↗ “R(Rituximab):375mg/m2 d0(first course),500mg/m2 d0(subsequent courses)” NCT03980002 ↗ “rituximab (R, 375 mg/m²) is given as an intravenous infusion on day 0” NCT07604987 ↗ “Rituximab, Cyclophosphamide, Doxorubicin, Vincristine and Prednisone” NCT06549595 ↗ “AlloNK, dosed after a conditioning regimen, combined with Rituximab.” NCT06991114 ↗ “cyclophosphamide. doxorubicin, vincristine , prednisone + Rituximab” NCT04243434 ↗ “rituximab, Two infusions separated by 2 weeks, Intravenous infusion” NCT01682512 ↗ “R-ICE consists of rituximab, etoposide, carboplatin and ifosfamide.” NCT03450343 ↗ “combined with R-EPOCH Rituximab, IV infusion on day 1 of each cycle” NCT02700022 ↗ “Prednison 100 mg absolute p.o. d 1-5 + Rituximab 375 mg/m² d 1 q3w” NCT00991211 ↗ “Rituximab, Cyclophosphamide, Adriamycin, Vincristine, Prednisolone” NCT02890602 ↗ “Rituximab was provided prior to transplant for PTLPD prophylaxis.” NCT00186823 ↗ “Rituximab, Cyclophosphamide, doxorubicin, vincristine, prednisone” NCT03995147 ↗ “either PF-05280586 or Rituxan (Rituximab) or MabThera (Rituximab)” NCT01526057 ↗ “Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisone” NCT06517511 ↗ “Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisone” NCT06647940 ↗ “Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisone” NCT07398638 ↗ “Rituximab 375 mg/m2 was administered intravenously every 28 days” PMID 35796785 ↗ Jul 2022 “Rituximab Doxorubicin Vincristine Cyclophosphamide Prednisolone” NCT01843868 ↗ “Rituximab is a chimeric human/murine IgG1 monoclonal antibody.” NCT00859001 ↗ “drug Nivolumab before and in combination with drug Rituximab” NCT03245021 ↗ “Rituximab: 375 mg/m2, intravenous drip, Day 1 of each cycle” NCT07499271 ↗ “rituximab 375 mg/m2 day 1 cyclophosphamide 750 mg/m2 day 1” NCT01502982 ↗ “Esc.R-BEACOPP as above plus Rituximab 375 mg/m2/ev/ die 1°” NCT00795613 ↗ “Rituximab by intravenous infusion over 6-8 hours on day 1” NCT00836173 ↗ “The antibody rituximab is given on the day of admission.” NCT01702961 ↗ “Rituximab in combination with idelalisib or bendamustine” NCT02970318 ↗ “another medication called rituximab may be used instead” NCT01275287 ↗ “rituximab (given intravenously at a dose of 500mg once)” NCT02834468 ↗ “Rituximab: 375 mg/m2 given intravenously (IV) on day 0” NCT04992377 ↗ “Rituximab 375 mg/m2 IV is given on Day 1 of each cycle” NCT07409428 ↗ “the anti-CD20 antibody Rituximab (375 mg/m2 d0 or d1)” NCT03129828 ↗ “Rituximab intravenous infusion dosage 375 mg/m² day 1” NCT01457144 ↗ “Revlimid 25mg PO d1-10 Plus Rituximab 375 mg/m2 IV d0” NCT03715309 ↗ “Rituximab 375 mg/m2 IV on Day 0 of each 21-day cycle.” NCT05933967 ↗ “Rituximab-ifosfamide, carboplatin, etoposide (R-ICE)” NCT03391466 ↗ “Rituximab 375 mg/m\^2 IVPB with premedications Day 1” NCT02633137 ↗ “Rituximab:375 mg/m2/ time, once a week for 4 times;” NCT05969522 ↗ “Rituximab with 12 x 2 Gy involved site radiotherapy” NCT05045664 ↗ “rituximab + dexamethasone + cytarabine + cisplatin” NCT02055924 ↗ “rituximab and/or dexamethasone and/or vincristine” NCT03236857 ↗ “Rituximab: 375 mg/m², intravenous infusion, Day 1” NCT07680933 ↗ “Rituximab 375mg/m2 i.v. on day 1 of every cycle.” NCT07570017 ↗ “Rituximab 375mg/m2 IV weekly x 4, start day -7” NCT01181258 ↗ “rituximab 375 mg/m2 IV Weekly x 4 1 cycle only” NCT00166439 ↗ “of rituximab (RTX) (Mabthera®) is non-inferior” NCT05116228 ↗ “Rituximab 375 mg/m²,intravenous ( iv ), day 0” NCT00946374 ↗ “rituximab (IV, 250 mg/m2 on days -21 and -14)” NCT00336843 ↗ “Rituximab: 375 mg/m2, IV, day 1 of each cycle” NCT03650933 ↗ “Rituximab 375mg/m² IV day 1 per 21-day cycle” NCT07538180 ↗ “Rituximab 375 mg/m2 on D1 (on D1/8/15 in C1)” NCT04066920 ↗ “375 mg/m2 intravenous on day 1 for rituximab” PMID 37011643 ↗ Mar 2023 “rituximab: 375 mg/m2 intravenously on day 7” NCT06445257 ↗ “Rituximab IV if LNH type B (375 mg/m²) day1” NCT00863460 ↗ “the anti-CD20 monoclonal antibody rituximab” NCT02012088 ↗ “steroids, IVIG, azathioprine, and rituximab” NCT03412188 ↗ “Methotrexate or leflunomide + rituximab or” NCT02714634 ↗ “Rituximab 375 mg/m2 IV Day 1, Cycles 1-6;” NCT02747732 ↗ “combined with rituximab 375mg/m2 IV day 0” NCT00854568 ↗ “Mabthera -Rituximab (375 mg/sm, D1)/cycle” NCT00842114 ↗ “Rituximab, 250 mg/m2 on days -21 and -14.” NCT00644371 ↗ “Rituximab (Innovent) 375 mg/m², iv Day 1” NCT07494565 ↗ “Rituximab,375mg/㎡, d1,intravenous drip” NCT06412068 ↗ “Rituximab vs DPP/DCEP-G vs observation” NCT03695055 ↗ “treatment rituximab 375 mg/m2,ivgtt D0” NCT03373019 ↗ “Day +90: rituximab (375mg/m2 IV once)” NCT03128996 ↗ “Rituximab (375 mg/m²) pre-operatively” NCT07519005 ↗ “RITUXIMAB Dosage: 375mg/m2, IV, day 1” NCT01361191 ↗ “Rituximab(B-NHL) 375 mg/m2/day IV d0” NCT01818908 ↗ “Venetoclax and rituximab association” NCT03455517 ↗ “Drug: RiTUXimab Injection [Rituxan]” NCT04542629 ↗ “Rituximab 375 mg/m2 IV on D0 or D1” NCT05966233 ↗ “Rituximab 375 mg/sqm iv day 0 or 1” NCT01805557 ↗ “* Rituximab 375 mg/m2, e.v. day 1” NCT02371161 ↗ “Rituximab Gemcitabine Oxaliplatin” NCT01670370 ↗ “Rituximab 375 mg/m²/d i.v. (d0,5)” NCT02531841 ↗ “EU-sourced rituximab (Mabthera®)” NCT04671420 ↗ “Rituximab (375mg/m\^2) on day 1;” NCT06244368 ↗ “* Rituximab i.v.: 375 mg/m2 (D0)” NCT05820841 ↗ “Rituximab: 375mg/m2 iv.drip D1;” NCT05577364 ↗ “CHOP-14- Rituximab x 8 courses” NCT00561379 ↗ “Rituximab at 375mg/m2 on day 1” NCT06290817 ↗ “Rituximab 375 mg/m² i.v. d0,14” NCT06830421 ↗ “(rituximab 375mg/m2 d0 ivgtt)” NCT03513601 ↗ “R-CHOP: Rituximab 375mg/m2 d0” NCT05164770 ↗ “Rituximab 375mg//m2, ivgtt,d1” NCT03201471 ↗ “Rituximab: 375 mg/m² day 1 iv” NCT02063685 ↗ “Rituximab (R) 375mg/m2 IV d0” NCT06158399 ↗ “Rituximab 375 mg/m2 D1, I.V.” NCT06255704 ↗ “rituximab 375 mg/m2 on day 1” NCT03392714 ↗ “R-CHOP:Rituximab 375mg/m2 d0” NCT05097443 ↗ “Rituximab 375 mg/m2 IV 0 day” NCT03479918 ↗ “* Rituximab 375 mg / m\^2,D1” NCT05257018 ↗ “Rituximab: 375 mg/m2 IV day0” NCT04432402 ↗ “rituximab 375 mg/m2,ivgtt D1” NCT03318835 ↗ “rituximab 375 mg/m2,ivgtt D1” NCT04164368 ↗ “rituximab infusion [Rituxan]” NCT05025423 ↗ “Rituximab 375 mg/m2 D1, I.V.” NCT04736914 ↗ “Rituximab: 375 mg/m2, IV, d1” NCT07059650 ↗ “* Rituximab 375mg/m2, IV, D1” NCT05245656 ↗ “Rituximab 375mg/m2, ivd, D1” NCT05093140 ↗ “Rituximab: 375 mg/m², Day 0” NCT07677813 ↗ “rituximab 375mg/m2 IV day 0” NCT01914718 ↗ “Rituximab:375mg/m2,ivgtt,D0” NCT02526823 ↗ “Rituximab:375mg/m2,ivgtt,D0” NCT04152577 ↗ “Rituximab intravenous drip” NCT06760039 ↗ “rituximab 500 mg/m2 day -1” NCT01582048 ↗ “rituximab 375mg/m2, iv d1” NCT06062641 ↗ “Drug: Rituximab Rituximab” NCT06486337 ↗ “Rituximab 375 mg/m2 d0 iv” NCT05347641 ↗ “Rituximab (375 mg/m2,d0)” NCT06569485 ↗ “* Rituximab * Cytarabine” NCT00801580 ↗ “rituximab 375mg/m2 day 0” NCT01804127 ↗ “Rituximab: 375 mg/m2, d0” NCT05974085 ↗ “rituximab: 375 mg/m2, D0” NCT06901999 ↗ “Rituximab-375 mg/m2 : D1” NCT01285765 ↗ “Rituximab 375mg/m2 IV D0” NCT05348213 ↗ “rituximab or biosimilar” NCT05468320 ↗ “incorporating rituximab” NCT04684979 ↗ “Rituximab 375 mg/m² Q3W” NCT04980859 ↗ “Rituximab 375 mg/m2 D1” NCT06750991 ↗ “Rituximab 375 mg/m2 D1” NCT06701357 ↗ “Rituximab 375mg/m2, D0” NCT05040555 ↗ “Rituximab 375mg/m2,d0” NCT04134247 ↗ “Rituximab (MabThera):” NCT00568477 ↗ “MabThera (rituximab)” NCT02371096 ↗ “rituximab (Rituxan®)” NCT04047628 ↗ “Rituximab Injection” NCT04083014 ↗ “rituximab 375 mg/m²” NCT04263584 ↗ “Rituximab: 375mg/m2” NCT07122609 ↗ “Rituxan (rituximab)” NCT03535298 ↗ “Drug: Rituximab” NCT01253460 ↗ “Drug: Rituximab” NCT03777085 ↗ “dd 2, Rituximab” NCT01516593 ↗ “• Rituximab” NCT07124078 ↗ “• Rituximab” NCT06821542 ↗ “* Rituximab” NCT02171104 ↗ “Rituximab” NCT03161457 ↗ “Rituximab” NCT03571308 ↗ |
| Known as | ABP 798 | “ABP 798” NCT03096782 ↗ |
| Known as | Acellbia | ClinicalTrials.gov intervention name — accepted as the source's own label NCT02744196 ↗ |
| Known as | CT-P10 | ClinicalTrials.gov intervention name — accepted as the source's own label NCT02149121 ↗ |
| Known as | EU-rituximab | “Reference product US- rituximab (Rituxan®) or EU-rituximab (MabThera®), 100mg or 500mg, concentrate for solution for infusion” NCT04268771 ↗ |
| Known as | EU-RTX | “Adults with active RA were treated with CT-P10, United States-sourced RTX (US-RTX; Rituxan®), or European Union-sourced RTX (EU-RTX; MabThera®) at weeks 0 and 2.” PMID 30010481 ↗ Jul 2018 |
| Known as | Halpryza | “Participants who experience life-threatening toxicities caused by uncontrollable proliferation of fhB7H3.CAR-Ts will receive infusion of Rituximab (Rituxan or Ruxience or Halpryza)” NCT05211557 ↗ |
| Known as | IDEC-102 | “Effect of Rituximab (IDEC-102) on Primary Humoral Response, Recall Response, and Maintenance of Acquired Immunity to Specific Antigens” NCT00090038 ↗1“Treatment of Relapsed Low-Grade or Follicular Lymphoma With Rituximab (Also Known as Rituxan, IDEC-C2B8, IDEC-102)” NCT00168740 ↗ |
| Known as | IDEC-C2B8 | “The double-blind, parallel-group comparison, investigators initiated phase II clinical trial of IDEC-C2B8 (Rituximab) in patients with Systemic sclerosis (DesiReS) trial showed...” PMID 35136981 ↗ Nov 20229“A Randomized, Phase III Trial to Determine the Effect of Consolidation With Rituximab (IDEC C2B8-Mabthera) in Patients With CD20+ Follicular or Mantle Cell Lymphoma Having...” NCT00003280 ↗ “Rituximab (IDEC-C2B8, Mabthera) in Patients With Hairy Cell Leukemia Relapsing After Treatment With 2-Chlorodeoxyadenosine (CDA)” NCT00003757 ↗ “Treatment of Relapsed Low-Grade or Follicular Lymphoma With Rituximab (Also Known as Rituxan, IDEC-C2B8, IDEC-102)” NCT00168740 ↗ “Rituximab (IDEC-C2B8) Plus GM-CSF in Patients With Follicular B-Cell Lymphoma” NCT01939730 ↗ “rituximab (IDEC-C2B8 monoclonal antibody; anti-CD20 monoclonal antibody)” NCT00003397 ↗ “chimeric anti-CD20 monoclonal antibody IDEC-C2B8 (rituximab) induction.” NCT00003248 ↗ “rituximab (IDEC-C2B8 monoclonal antibody)” NCT00003605 ↗ “Drug: rituximab / IDEC-C2B8” NCT02265731 ↗ “IDEC-C2B8 (rituximab)” NCT00298272 ↗ |
| Known as | intrathecal rituximab (Mabthera) | “intrathecal rituximab (Mabthera)” NCT02545959 ↗ |
| Known as | LD-RTX | “all-trans retinoic acid (ATRA) plus low-dose rituximab (LD-RTX) with LD-RTX monotherapy” PMID 34665865 ↗ Jan 2022 |
| Known as | MabThera | “An Open Label, Multicenter, Non Randomized Phase II Study to Evaluate Antitumor Efficacy and Safety of GM-CSF (Sargramostim, Leukine®) Associated With RCHOP Chemotherapy and...” NCT00896519 ↗91“This is an open label, phase II study to evaluate the capacity of Rituximab (Mabthera®) plus Lenalidomide (Revlimid®) to induce objective responses in patients with Mucosa...” NCT01611259 ↗ “A Randomized, Phase III Trial to Determine the Effect of Consolidation With Rituximab (IDEC C2B8-Mabthera) in Patients With CD20+ Follicular or Mantle Cell Lymphoma Having...” NCT00003280 ↗ “Subjects were offered ≤3 additional courses of treatment of PF-05280586, with or without a single transition from rituximab in Europe (rituximab-EU; MabThera) or the US...” PMID 29692005 ↗ Nov 2018 “Treatment with \[90Y\]-ibritumomab tiuxetan is preceded by an infusion of rituximab (Rituxan, Mabthera) in order to optimize the biodistribution of radiolabeled antibody by...” NCT00859001 ↗ “Advanced Follicular Lymphoma Evaluating the Benefit of Maintenance Therapy With Rituximab (MabThera®) After Induction of Response With Chemotherapy Plus Rituximab in Comparison...” NCT00140582 ↗ “Treatment with [90Y]-ibritumomab tiuxetan is preceded by an infusion of rituximab (Rituxan, Mabthera) in order to optimize the biodistribution of radiolabeled antibody by...” NCT00850512 ↗ “OBJECTIVE: This study aimed to compare the pharmacokinetic, pharmacodynamic and safety profiles of HLX01 (a rituximab biosimilar) and reference rituximab sourced from China...” PMID 34321836 ↗ Jun 2021 “Randomized Study of Rituximab (Mabthera) in Patients With Relapsed Follicular Lymphoma Prior to High-Dose Therapy as In Vivo Purging and to Maintain Remission Following...” NCT00005589 ↗ “The CD20-specific monoclonal antibody rituximab (MabThera(®), Rituxan(®)) is widely used as the backbone of treatment for patients with hematologic disorders.” PMID 24265828 ↗ Nov 2013 “Treatment: Controlled ovarian hyperstimulation before and four months after an infusion of 1-gram rituximab (Mabthera®) twice with two weeks interval.” NCT05586737 ↗ “A course of MabThera® (Rituximab, Roche) in rheumatoid arthritis patients consists of two 1000 mg intravenous infusions with two weeks interval.” NCT02468791 ↗ “High Dose Dexamethasone in Combination With Rituximab (MabThera®)in Patients With Newly Diagnosed Idiopathic Thrombocytopenic Purpura (ITP)” NCT00909077 ↗ “Rituximab (MabThera, F. Hoffmann-La Roche Ltd., Basel, Switzerland) 375 mg/m² every 3 months for 24 months (8 infusions) or observation” NCT01118234 ↗ “patients will receive 375 mg/m2 of rituximab (US, Canada - Rituxan®; EU - Mabthera®), given as an IV infusion once weekly for 4 weeks.” NCT00078598 ↗ “Rituximab (IDEC-C2B8, Mabthera) in Patients With Hairy Cell Leukemia Relapsing After Treatment With 2-Chlorodeoxyadenosine (CDA)” NCT00003757 ↗ “different treatment regimens of rituximab (MabThera®/Rituxan®), corticosteroids, and placebo, combined with methotrexate (MTX)” NCT00074438 ↗ “Reference product US- rituximab (Rituxan®) or EU-rituximab (MabThera®), 100mg or 500mg, concentrate for solution for infusion” NCT04268771 ↗ “A Study of MabThera (Rituximab) in Patients With Rheumatoid Arthritis Who Have Failed on One Prior Anti-TNF Therapy (RESET)” NCT01272908 ↗ “systemic treatment with the anti CD20 antibody Rituximab (Mabthera(R)) in combination with involved field radiotherapy” NCT00509184 ↗ “Patients will receive Rituximab (Mabthera) at 375 mg/m2, once a week during 4 weeks, administered in IV infusion” NCT00180895 ↗ “Randomization between Mabthera (rituximab) or no Mabthera during all induction and consolidation courses.” NCT00327678 ↗ “Rituximab (Mabthera®) will be given as 1000mg at weeks 0 and 2, and then repeated at weeks 24 and 26.” NCT01638715 ↗ “Safety and Efficacy of Revlimid® (Lenalidomide) With Mabthera® (Rituximab) in Non-Hodgkin's Lymphoma” NCT01939327 ↗ “NIST and Rituximab: 500 Mg and 100Mg in solution to be diluted for IV infusion (Mabthera®)” NCT01508468 ↗ “Rituximab (Mabthera) is a chimeric monoclonal antibody directed against CD20 antigen” NCT00892827 ↗ “The Chimeric Anti-CD20 Monoclonal Antibody (Mabthera) During Sequential Chemotherapy” NCT00012051 ↗ “Phase II Study of Rituximab (Rituxan, Mabthera) in Waldenstrom's Macroglobulinemia” NCT00004889 ↗ “Two intravenous perfusions of 1 g of Rituximab (Mabthera ®) at W0 and W2” NCT03154385 ↗ “MabThera® 500 mg/m\^2 or 1000 mg administered by IV on Day 1 and Day 15” NCT01390441 ↗ “Efficiency and Tolerance of Rituximab (mabthéra) in Bullous Pemphigoid” NCT00525616 ↗ “Combination Rituxan (Rituximab, Mabthera) and Fludarabine Therapy” NCT00020800 ↗ “Rituximab (Mabthera®, Roche Pty Ltd, Basel, Switzerland)” NCT01482754 ↗ “rituximab (Mabthera®), 1000 mg at day 1 and day 15” NCT01181154 ↗ “Maintenance Treatment With Rituximab (MabThera®)” NCT00662948 ↗ “Originator rituximab - Rituxan ® or MabThera ®” NCT02514772 ↗ “of rituximab (RTX) (Mabthera®) is non-inferior” NCT05116228 ↗ “Mabthera -Rituximab (375 mg/sm, D1)/cycle” NCT00842114 ↗ “Drug: rituximab [MabThera/Rituxan]” NCT02013817 ↗ “Drug: rituximab [MabThera/Rituxan]” NCT02006706 ↗ “Mabthera, Rituximab 1000 mg I.V.” NCT00936546 ↗ “Rituximab (mabthera) Injection” NCT00740948 ↗ “Rituximab (MabThera or CT-P10)” NCT01873443 ↗ “Rituximab (Mabthera) 500mg/m2” NCT00504491 ↗ “rituximab [MabThera/Rituxan]” NCT00502840 ↗ “rituximab [MabThera/Rituxan]” NCT01117129 ↗ “rituximab [MabThera/Rituxan]” NCT00422942 ↗ “rituximab [MabThera/Rituxan]” NCT01998893 ↗ “MabThera/Rituxan (rituximab)” NCT01388959 ↗ “rituximab [MabThera/Rituxan]” NCT00738374 ↗ “rituximab [MabThera/Rituxan]” NCT00422383 ↗ “rituximab [MabThera/Rituxan]” NCT00430352 ↗ “rituximab [MabThera/Rituxan]” NCT00269113 ↗ “rituximab [MabThera/Rituxan]” NCT01000610 ↗ “rituximab [MabThera/Rituxan]” NCT00472420 ↗ “rituximab [MabThera/Rituxan]” NCT01392716 ↗ “rituximab [MabThera/Rituxan]” NCT00576433 ↗ “rituximab [MabThera/Rituxan]” NCT00502996 ↗ “rituximab (MabThera/Rituxan)” NCT01938001 ↗ “rituximab [MabThera/Rituxan]” NCT01332994 ↗ “Rituximab [MabThera/Rituxan]” NCT00503425 ↗ “rituximab [MabThera/Rituxan]” NCT00517699 ↗ “rituximab [Mabthera/Rituxan]” NCT01144364 ↗ “Drug: Rituximab (Mabthera)” NCT00344149 ↗ “Rituximab (MabThera):” NCT00568477 ↗ “rituximab [MabThera]” NCT02079532 ↗ “Rituximab (Mabthera)” NCT06714838 ↗ “Rituximab (Mabthera)” NCT07035561 ↗ “MabThera (rituximab)” NCT00426543 ↗ “Mabthera (Rituximab)” NCT01277172 ↗ “Rituximab (mabthéra)” NCT00784589 ↗ “Mabthera i.v.: 200/0” NCT03963024 ↗ |
| Known as | mabthera equals Rituximab | “mabthera equals Rituximab” NCT01134432 ↗ |
| Known as | MabThera for Rituximab | “MabThera for Rituximab” NCT05063513 ↗ |
| Known as | Mabthera(R) | “systemic treatment with the anti CD20 antibody Rituximab (Mabthera(R)) in combination with involved field radiotherapy” NCT00509184 ↗ |
| Known as | MabThera/Rituxan | “MabThera/Rituxan (rituximab) in combination with CHOP chemotherapy” NCT01649856 ↗1“MabThera/Rituxan” NCT01126541 ↗ |
| Known as | NSC #687451 | “Randomized Phase III Trial Of Rituximab (NSC #687451) And Autologous Stem Cell Transplantation For B Cell Diffuse Large Cell Lymphoma” NCT00052923 ↗1“Chimeric Anti-CD20 Monoclonal Antibody IDEC-C2B8 (Rituximab) [NSC# 687451] Induction” NCT00003248 ↗ |
| Known as | PBO-326 | “PBO-326 (Rituximab)” NCT01277172 ↗ |
| Known as | Radiotherapy, rituximab and DC | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01926639 ↗ |
| Known as | Ristova | “Participants will be treated with rituximab (Ristova) and glucocorticoids.” NCT02115997 ↗ |
| Known as | RIT | “We aimed to compare the efficacy of azathioprine (AZA) and rituximab (RIT) as maintenance therapy in NMOSD patients.” PMID 28831548 ↗ Aug 2017 |
| Known as | Rituxan | “Subjects were offered ≤3 additional courses of treatment of PF-05280586, with or without a single transition from rituximab in Europe (rituximab-EU; MabThera) or the US...” PMID 29692005 ↗ Nov 201883“Treatment with \[90Y\]-ibritumomab tiuxetan is preceded by an infusion of rituximab (Rituxan, Mabthera) in order to optimize the biodistribution of radiolabeled antibody by...” NCT00859001 ↗ “The goal of this clinical research is to see if Rituxan (rituximab) therapy given after high dose chemotherapy and transplant of a patients own stem cells will prevent or delay...” NCT01103388 ↗ “This is a Phase I/II , single agent study which will evaluate the safety and feasibility of subcutaneous rituximab (Rituxan) administered at 20 mg/day three times a week for 12...” NCT00366418 ↗ “Treatment with [90Y]-ibritumomab tiuxetan is preceded by an infusion of rituximab (Rituxan, Mabthera) in order to optimize the biodistribution of radiolabeled antibody by...” NCT00850512 ↗ “The treatment combination of Rituxan® (rituximab) and fludarabine has previously been reported to produce a high percentage of responses with less toxicity than other...” NCT00078234 ↗ “Participants who experience life-threatening toxicities caused by uncontrollable proliferation of fhB7H3.CAR-Ts will receive infusion of Rituximab (Rituxan or Ruxience or Halpryza)” NCT05211557 ↗ “The purpose of this study is to reduce the symptoms of OMS by testing rituximab (Rituxan®), to remove B lymphocytes that make antibodies and trigger brain inflammation.” NCT00244361 ↗ “Rituximab (Rituxan) for the Prevention of EBV-LPD Epstein Barr Virus (EBV) Lymphoproliferative Disorder Post T Cell Depleted Unrelated and HLA Mis-matched Related HSCT” NCT00648037 ↗ “The CD20-specific monoclonal antibody rituximab (MabThera(®), Rituxan(®)) is widely used as the backbone of treatment for patients with hematologic disorders.” PMID 24265828 ↗ Nov 2013 “A Phase I/II Trial of IDEC-114 (Anti-CD80 Monoclonal Antibody) in Combination With Rituxan® for Patients With Relapsed or Refractory, Follicular Lymphoma” NCT00048555 ↗ “In this research study, the investigators are adding the drug rituximab (Rituxan) to the drug cytarabine for the stem cell mobilization process.” NCT01182415 ↗ “patients will receive 375 mg/m2 of rituximab (US, Canada - Rituxan®; EU - Mabthera®), given as an IV infusion once weekly for 4 weeks.” NCT00078598 ↗ “Comparing Interleukin-2 (IL-2) Combined With Rituximab (Rituxan) to Rituximab Alone in Subjects With Non-Hodgkin's Lymphoma (NHL)” NCT00100737 ↗ “different treatment regimens of rituximab (MabThera®/Rituxan®), corticosteroids, and placebo, combined with methotrexate (MTX)” NCT00074438 ↗ “Reference product US- rituximab (Rituxan®) or EU-rituximab (MabThera®), 100mg or 500mg, concentrate for solution for infusion” NCT04268771 ↗ “A Randomized Trial Comparing Higher Doses of Rituximab (Rituxan) With Standard Doses of Rituxan in Combination With CVP” NCT00161564 ↗ “Treatment of Relapsed Low-Grade or Follicular Lymphoma With Rituximab (Also Known as Rituxan, IDEC-C2B8, IDEC-102)” NCT00168740 ↗ “A Phase II Trial of Alemtuzumab (Campath-1H) and Rituximab (Rituxan) in Patients With Previously Untreated CLL” NCT00858117 ↗ “Prevention of Cardiac Allograft Vasculopathy Using Rituximab (Rituxan) Therapy in Cardiac Transplantation” NCT01278745 ↗ “Rituxan is a mouse/human monoclonal antibody and reacts with the CD20 antigens found on lymphoma cells” NCT00005592 ↗ “Rituximab (Mabthera/Rituxan®) will be administered as per local practice” NCT04833114 ↗ “Combination Rituxan (Rituximab, Mabthera) and Fludarabine Therapy” NCT00020800 ↗ “Bevacizumab (Bevacizumab™)- Rituximab (Rituxan®)-CHOP (RA-CHOP)” NCT00401817 ↗ “Originator rituximab - Rituxan ® or MabThera ®” NCT02514772 ↗ “Anti-CD20 Moab (IDEC C2B8, Rituximab, Rituxan)” NCT00003397 ↗ “Drug: RiTUXimab Injection [Rituxan]” NCT04542629 ↗ “Drug: rituximab [MabThera/Rituxan]” NCT02013817 ↗ “Drug: rituximab [MabThera/Rituxan]” NCT02006706 ↗ “rituximab [MabThera/Rituxan]” NCT00422383 ↗ “rituximab [MabThera/Rituxan]” NCT01117129 ↗ “rituximab [MabThera/Rituxan]” NCT01998893 ↗ “rituximab [Mabthera/Rituxan]” NCT01144364 ↗ “MabThera/Rituxan (rituximab)” NCT01388959 ↗ “rituximab [MabThera/Rituxan]” NCT00738374 ↗ “rituximab [MabThera/Rituxan]” NCT00269113 ↗ “rituximab [MabThera/Rituxan]” NCT00472420 ↗ “rituximab [MabThera/Rituxan]” NCT01000610 ↗ “rituximab [MabThera/Rituxan]” NCT01392716 ↗ “rituximab [MabThera/Rituxan]” NCT00576433 ↗ “rituximab [MabThera/Rituxan]” NCT00502840 ↗ “rituximab [MabThera/Rituxan]” NCT00502996 ↗ “rituximab [MabThera/Rituxan]” NCT01332994 ↗ “rituximab [MabThera/Rituxan]” NCT00422942 ↗ “Rituximab [MabThera/Rituxan]” NCT00503425 ↗ “rituximab [MabThera/Rituxan]” NCT00517699 ↗ “rituximab [MabThera/Rituxan]” NCT00430352 ↗ “Drug: Rituximab (Rituxan)” NCT00724971 ↗ “rituximab (Rituxan )” NCT00022971 ↗ “Rituxan (rituximab)” NCT00057343 ↗ “Ruxience or Rituxan” NCT03530683 ↗ “Rituxan” NCT00331006 ↗ |
| Known as | Rituxan (rituximab) | “Rituxan (rituximab)” NCT03535298 ↗ |
| Known as | RITUXAN (Trademark) | “This study will test whether rituximab (RITUXAN (Trademark)) can relieve symptoms of stiff person syndrome (SPS), a progressive disease that causes stiffness of the muscles and...” NCT00091897 ↗ |
| Known as | Rituxan(R), MabThera(R) = Rituximab | “Rituxan(R), MabThera(R) = Rituximab” NCT00991211 ↗ |
| Known as | Rituximab (Mabthera; Rituxan) 375 mg/m² | “Rituximab (Mabthera®; Rituxan®) 375 mg/m²” NCT02157181 ↗ |
| Known as | Rituximab Biosimilar | ClinicalTrials.gov intervention name — accepted as the source's own label NCT06890884 ↗ |
| Known as | Rituximab Biosimilar RTXM83 | “Rituximab Biosimilar RTXM83” NCT03096782 ↗ |
| Known as | rituximab biosimilar TQB2303 | “rituximab biosimilar TQB2303” NCT02727803 ↗ |
| Known as | rituximab IDEC-C2B8 | “rituximab IDEC-C2B8” NCT00089284 ↗ |
| Known as | RiTUXimab Injection | “Drug: RiTUXimab Injection” NCT06341205 ↗ |
| Known as | rituximab-abbs | “rituximab-abbs” NCT02727803 ↗ |
| Known as | rituximab-CN | “OBJECTIVE: This study aimed to compare the pharmacokinetic, pharmacodynamic and safety profiles of HLX01 (a rituximab biosimilar) and reference rituximab sourced from China...” PMID 34321836 ↗ Jun 2021 |
| Known as | rituximab-EU | “MabThera® (rituximab-EU) concentrate for solution for infusion 375mg/m2 administered via IV infusion on Days 1, 8, 15, and 22” NCT02213263 ↗ |
| Known as | Rituximab-pvvr | ClinicalTrials.gov intervention name — accepted as the source's own label NCT03929601 ↗ |
| Known as | Rituximab-US | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01643928 ↗ |
| Known as | Rituximab: MABTHERA | “Rituximab (MabThera)” NCT00937131 ↗4“Rituximab (MabThera)” NCT01307605 ↗ “Rituximab (Mabthera)” NCT00646750 ↗ “Rituximab (Mabthera)” NCT00644371 ↗ “Rituximab: MABTHERA” NCT01185262 ↗ |
| Known as | Rituximab:Rituxan | “rituximab (Rituxan®)” NCT04047628 ↗4“Rituximab - Rituxan” NCT01001780 ↗ “Rituximab (Rituxan)” NCT01527422 ↗ “Rituximab (Rituxan)” NCT00250926 ↗ “Rituximab:Rituxan” NCT01449344 ↗ |
| Known as | Rituximab=CT-P10 | “Rituximab=CT-P10” NCT01873443 ↗ |
| Known as | RTX | “In vitro, immune complexes (ICx) trigger NET formation while NET-derived DNA is a postulated autoantigen for anti-nuclear autoantibodies (ANAs), found in SLE. Based on these...” PMID 29636274 ↗ Apr 201829“Both rituximab (RTX) and cyclophosphamide (CYC) are effectively used in combination with steroids as remission induction therapy for patients with antineutrophil cytoplasmic...” PMID 36130755 ↗ Sep 2022 “OBJECTIVE To test whether Rituximab (RTX) is efficacious to achieve complete renal response (CR) in Lupus Nephritis (LN) patients with persistent proteinuria (≥1g/d) despite at...” NCT01673295 ↗ “A pilot study previously demonstrated that thrice-weekly, fractionated-dose intravenous rituximab (RTX) limits CD20 loss from chronic lymphocytic leukemia (CLL) B cells,...” PMID 19679883 ↗ Aug 2009 “To assess the maximum tolerated dose (MTD) of temozolomide (TMZ) in combination with methotrexate (MTX) and rituximab (RTX) when administered prior to twice daily fractionated...” NCT00068250 ↗ “Rituximab (RTX) is a chimeric anti-CD20 monoclonal antibody that depletes B cells and is effective in numerous autoimmune diseases including antineutrophil cytoplasmic antibody...” PMID 21325353 ↗ Feb 2011 “CT-P10 is a biosimilar of innovator rituximab (RTX), a biological therapy used to treat patients with rheumatoid arthritis (RA) who have responded inadequately to anti-tumor...” PMID 28612179 ↗ Aug 2017 “OBJECTIVE: To characterize the safety of rituximab (RTX) in combination with biologic disease-modifying antirheumatic drugs (DMARD) in patients with rheumatoid arthritis (RA).” PMID 23547218 ↗ Apr 2013 “prospectively evaluate the efficacy and safety of rituximab (RTX) versus placebo in a broad range of progressive ILD outside sarcoidosis and connective tissue diseases.” PMID 39693827 ↗ Nov 2024 “Patients were randomized to either TNFi (infliximab, INF), anti-IL-6 (tocilizumab, TCZ), CTLA4-Ig (abatacept, ABA) or anti-CD20 (rituximab, RTX) in addition to MTX.” PMID 34792562 ↗ Jul 2022 “Those with an MSD underwent allogeneic HCT (n = 8) with the FCR preparative regimen (fludarabine, cyclophosphamide [Cy], rituximab [RTX])” PMID 21073974 ↗ Nov 2010 “Rituximab (RTX) is a monoclonal antibody directed against CD20 antigen on B cells which has been successfully employed in anti-MuSK-Ab+MG” PMID 32098874 ↗ Feb 2020 “Rituximab (RTX) has been used off-label for years to treat ITP but there are limited studies about its efficacy and safety in children.” PMID 34962697 ↗ Dec 2021 “clinical efficacy and safety of rituximab (RTX) treatment in 40 patients with vimentin antibody (VIMA)-related diseases.” NCT07051070 ↗ “Rituximab (RTX) effectively prevents relapses in patients with complicated steroid-sensitive nephrotic syndrome (SSNS).” PMID 36223961 ↗ Oct 2022 “Impact of Rituximab (RTx) Induction and Living Donation on Immunoregulation and Virus Control in Renal Transplantation” NCT01136395 ↗ “Rituximab (Rtx) antibody infusions will be administered on Day 1, 2, 3 (cycle 1) and Day 1 (cycles 2 to 4).” NCT01576588 ↗ “Lenalidomide (LEN) and rituximab (RTX) have independently improved progression-free survival (PFS) in CLL” PMID 38856101 ↗ Jun 2024 “Rituximab (RTX) improves the outcome in patients with systemic diffuse large B-cell lymphoma (DLBCL)” PMID 27123138 ↗ Mar 2016 “anti-CD20 biotherapeutics (especially Rituximab, RTX)) is gaining popularity as first-line therapy” NCT05532111 ↗ “Lymphoma Protocol consisting of four weekly doses of 375 mg/m2 of rituximab (RTX)” NCT06680349 ↗ “Rituximab (RTX) will be given as a single intravenous (IV) dose of 375 mg/m2.” NCT05679336 ↗ “Rituximab (RTX) is an effective second-line treatment.” PMID 41741872 ↗ Feb 2026 “of rituximab (RTX) (Mabthera®) is non-inferior” NCT05116228 ↗ “Rituximab (RTX) and Azathioprine (AZA)” NCT02789397 ↗ “innovator rituximab (RTX)” PMID 28600696 ↗ Aug 2017 “Rituximab (RTX)” NCT07694414 ↗ “rituximab (RTX)” PMID 34164952 ↗ Dec 2021 “rituximab (RTX)” NCT02900976 ↗ “Rituximab (RTX)” NCT02763319 ↗ |
| Known as | RTX-EU | “Rituxan® [RTX-US] and MabThera® [RTX-EU]” PMID 32052313 ↗ Apr 2020 |
| Known as | RTX-US | “Rituxan® [RTX-US] and MabThera® [RTX-EU]” PMID 32052313 ↗ Apr 2020 |
| Known as | RTXM83 | “RTXM83” NCT02727803 ↗ |
| Known as | Ruxience | “Participants who experience life-threatening toxicities caused by uncontrollable proliferation of fhB7H3.CAR-Ts will receive infusion of Rituximab (Rituxan or Ruxience or Halpryza)” NCT05211557 ↗ |
| Known as | Truxima | “Rituximab (Truxima) 375mg/m2 IV Weekly (X4)” NCT03578198 ↗5“Drug: RiTUXimab Injection [Truxima]” NCT05191225 ↗ “TRUXIMA®” NCT07634471 ↗ “Truxima” NCT02727803 ↗ “Truxima” NCT04189588 ↗ |
| Known as | US-rituximab | “Reference product US- rituximab (Rituxan®) or EU-rituximab (MabThera®), 100mg or 500mg, concentrate for solution for infusion” NCT04268771 ↗ |
| Known as | US-RTX | “Adults with active RA were treated with CT-P10, United States-sourced RTX (US-RTX; Rituxan®), or European Union-sourced RTX (EU-RTX; MabThera®) at weeks 0 and 2.” PMID 30010481 ↗ Jul 2018 |
| Known as | ◦Drug: Rituximab | “◦Drug: Rituximab” NCT01983761 ↗ |
| Action | Deplete | “Rituximab, a CD20 monoclonal antibody, may result in eradication of the monoclonal B cells.” PMID 18067008 ↗ Dec 2007 |
| Modality | Monoclonal antibody | “rituximab, the humanized monoclonal antibody against the CD20 receptor” NCT00001337 ↗ |
| Route | Intravenous | “Rituximab 375 mg/m\^2 intravenous (IV) on day 1” NCT00001337 ↗ |
| Target | CD20 | “Chimeric Anti-CD20 Antibody” NCT05052528 ↗ |