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Global R&D Pipeline
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Global R&D Pipeline

CD20
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Total number of drugs
337
Phase II and later clinical stages
16.3%
Involving companies
462
Main therapeutic areas
Neoplasms
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Molecule Info
R&D and Market Info
ADC Info
DrugDrug Name EnDrug TypeTreatment FieldMechanism of ActionOriginatorDeveloperIndicationHighest Development StageHighest Development Stage (China)Approved Countries/RegionsApproved TimeApproved Time (China)Special ReviewADC TypeADC LinkerADC PayloadADC DARDrug NameAntibody TypeADC Linking SiteOperation
EpcoritamabEpcoritamabBispecific T-cell Engager (BiTE)Neoplasms Immune System Diseases Hemic and Lymphatic Diseases Other Diseases Infectious Diseases Cardiovascular DiseasesCD20 inhibitors CD3 stimulantsGenmab A/SAbbVie, Inc. Genmab, Inc. Genmab A/S AbbVie Pharmaceutical Trading (Shanghai) Co. Ltd. AbbVie Deutschland GmbH & Co. KG Vetter Pharma-Fertigung GmbH & Co. KG Genmab BVApprovedNDA/BLAUnited States European Union Japan United Kingdom Canada Iceland South Korea Liechtenstein Norway2023-05-19-Accelerated Approval(United States) Breakthrough Therapy(United States) Conditional marketing approval(European Union) Orphan Drug(Australia) Orphan Drug(European Union) Orphan Drug(United States) Priority Review(China) Priority Review(United States)----Epcoritamab--
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OdronextamabOdronextamabBispecific T-cell Engager (BiTE)Neoplasms Immune System Diseases Hemic and Lymphatic Diseases Other DiseasesCD20 inhibitors CD3 stimulants ADCC CD20-directed cytolytic effectsRegeneron Pharmaceuticals, Inc.Regeneron Pharmaceuticals, Inc. Zai Lab (Shanghai) Co., Ltd. Regeneron Ireland DACApprovedPhase 3European Union Iceland Liechtenstein Norway2024-08-22-Fast Track(United States) Orphan Drug(European Union) Orphan Drug(United States) Priority Review(United States)----Odronextamab--
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Ibritumomab TiuxetanIbritumomab TiuxetanRadiolabeled antibody Therapeutic radiopharmaceuticalsNeoplasms Immune System Diseases Hemic and Lymphatic DiseasesCD20 inhibitorsBiogen, Inc.Ceft Biopharma s.r.o. CASI PHARMACEUTICALS INC Mundipharma KK Spectrum Pharmaceuticals, Inc.ApprovedPending (in IND Approval)United States European Union Japan Hong Kong Iceland Liechtenstein Norway2002-02-19-Accelerated Approval(United States) Orphan Drug(United States)IbritumomabMX-DTPA90 Y-Ibritumomab TiuxetanIgG1 - kappa-
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OfatumumabOfatumumabMonoclonal antibodyNeoplasms Immune System Diseases Nervous System Diseases Hemic and Lymphatic Diseases Other DiseasesCD20 inhibitors ADCC CD20-directed cytolytic effects Complement dependent cytotoxicity (CDC) effectsGenmab A/SNovartis AG Novartis Pharma AG Novartis Pharmaceuticals Corp. GSK Plc Novartis Europharm Ltd. Celgene Corp. Novartis Pharmaceuticals Canada, Inc.ApprovedApprovedUnited States China European Union Japan Canada Iceland Liechtenstein Norway2009-10-262021-12-20Accelerated Approval(United States) Breakthrough Therapy(United States)----Ofatumumab--
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ObinutuzumabObinutuzumabMonoclonal antibodyNeoplasms Immune System Diseases Hemic and Lymphatic Diseases Skin and Musculoskeletal Diseases Urogenital Diseases Other Diseases Nervous System Diseases Digestive System Disorders Infectious DiseasesCD20 inhibitors ADCC CD20-directed cytolytic effects Complement dependent cytotoxicity (CDC) effectsRoche Glycart AGAbbVie, Inc. F. Hoffmann-La Roche Ltd. Roche Diagnostics GmbH Celgene Corp. Acerta Pharma BV Genentech, Inc. Janssen-Cilag Ltd. Hoffmann-La Roche, Inc. Roche China Holding Ltd. Biogen, Inc. Pharmacyclics LLC Roche Pharma AG Nippon Shinyaku Co., Ltd. Bristol Myers Squibb Co. Roche Registration GmbH Chugai Pharmaceutical Co., Ltd. Shanghai Roche Pharmaceuticals Ltd. Roche Holding AG Janssen LP Roche Pharma (Schweiz) AGApprovedApprovedUnited States China European Union Japan Canada Australia Iceland South Korea Liechtenstein Norway2013-11-012021-06-01Breakthrough Therapy(United States) Orphan Drug(European Union) Orphan Drug(United States) Priority Review(China)----Obinutuzumab--
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Rituximab/HyaluronidaseRituximab/HyaluronidaseMonoclonal antibody EnzymeNeoplasms Immune System Diseases Hemic and Lymphatic Diseases Other DiseasesCD20 inhibitors Hyaluronic acid modulators ADCC CD20-directed cytolytic effects Complement dependent cytotoxicity (CDC) effectsRoche Holding AGGenentech, Inc. Roche Holding AGApprovedApprovedUnited States China Canada2016-11-222024-04-07-----Rituximab/Hyaluronidase--
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OcrelizumabOcrelizumabMonoclonal antibodyImmune System Diseases Nervous System Diseases Other DiseasesCD20 inhibitors ADCC CD20-directed cytolytic effects Complement dependent cytotoxicity (CDC) effectsGenentech, Inc. Biogen Idec Ltd.Hoffmann-La Roche, Inc. Hoffmann-La Roche Ltd. Roche Registration GmbH Roche Products Ltd. Roche Pharma (Schweiz) AG Roche Holding AG Genentech, Inc. Roche Korea Co., Ltd. Roche Pharma AGApprovedApprovedUnited States China European Union United Kingdom Canada Australia United Arab Emirates Switzerland Iceland South Korea Liechtenstein Norway2017-03-282025-03-25Breakthrough Therapy(United States) Fast Track(United States)----Ocrelizumab--
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RipertamabRipertamabMonoclonal antibodyNeoplasms Immune System Diseases Hemic and Lymphatic DiseasesCD20 inhibitors ADCC CD20-directed cytolytic effects Complement dependent cytotoxicity (CDC) effectsSinocelltech Group Ltd.Sinocelltech Group Ltd.ApprovedApprovedChina2022-08-232022-08-23-----Ripertamab--
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MosunetuzumabMosunetuzumabBispecific T-cell Engager (BiTE)Neoplasms Immune System Diseases Hemic and Lymphatic Diseases Other Diseases Skin and Musculoskeletal DiseasesCD20 inhibitors CD3 stimulantsGenentech, Inc.Hoffmann-La Roche, Inc. Genentech, Inc. F. Hoffmann-La Roche Ltd. Roche Registration GmbH Chugai Pharmaceutical Co., Ltd. Roche Holding AG Roche China Holding Ltd. Biogen, Inc. Hoffmann-La Roche Ltd. Adaptive Biotechnologies Corp. Roche Pharma (Schweiz) AGApprovedApprovedUnited States China European Union Japan Iceland Liechtenstein Norway2022-06-032024-12-17Accelerated Approval(United States) Breakthrough Therapy(United States) Conditional marketing approval(European Union) Orphan Drug(European Union) Orphan Drug(United States) Priority Review(China) Priority Review(United States) Conditional marketing approval(China)----Mosunetuzumab--
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ZuberitamabZuberitamabMonoclonal antibodyNeoplasms Immune System Diseases Hemic and Lymphatic Diseases Urogenital Diseases Other Diseases Skin and Musculoskeletal DiseasesCD20 inhibitors ADCC Complement dependent cytotoxicity (CDC) effectsBioRay Biopharmaceutical Co., Ltd.BioRay Biopharmaceutical Co., Ltd.ApprovedApprovedChina Macao2023-05-122023-05-12-----Zuberitamab--
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Total 337 data
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