Drugs / Trastuzumab
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Trastuzumab

Monoclonal antibody targets ERBB2

Developed for
breast cancer · HER2 positive breast carcinoma · female breast carcinoma · gastric cancer · breast neoplasm · gastroesophageal junction adenocarcinoma · colorectal cancer · non-small cell lung carcinoma
+128 more · cancer · breast carcinoma · esophageal cancer · gastric adenocarcinoma · male breast carcinoma · metastatic malignant neoplasm · estrogen-receptor positive breast cancer · hormone receptor-positive breast cancer · triple-negative breast carcinoma · gastroesophageal adenocarcinoma · inflammatory breast carcinoma · malignant pancreatic neoplasm · metastatic malignant neoplasm in the brain · cancer of unknown primary site · invasive breast carcinoma · biliary tract cancer · carcinoma · endometrial cancer · esophageal adenocarcinoma · gastroesophageal cancer · Her2-receptor negative breast cancer · lung cancer · metastatic neoplasm · neoplastic meningitis · ovarian cancer · urothelial carcinoma · cholangiocarcinoma · endometrial carcinoma · gastric carcinoma · hematopoietic and lymphoid cell neoplasm · neoplasm · plasma cell myeloma · progesterone-receptor positive breast cancer · rectum adenocarcinoma · bladder transitional cell carcinoma · breast adenocarcinoma · breast carcinoma by gene expression profile · cervical carcinoma · estrogen-receptor negative breast cancer · head and neck cancer · head and neck squamous cell carcinoma · melanoma · non-Hodgkin lymphoma · ovarian carcinoma · prostate carcinoma · renal pelvis/ureter urothelial carcinoma · sarcoma · urinary bladder carcinoma · adenocarcinoma · biliary tract neoplasm · breast carcinoma in situ · carcinoma of esophagus · cervical cancer · colon adenocarcinoma · colorectal neoplasm · ductal breast carcinoma in situ · esophageal squamous cell carcinoma · extrahepatic bile duct carcinoma · gallbladder cancer · gallbladder carcinoma · gastric neoplasm · high grade malignant neoplasm · metastasis from malignant tumor of colon · posterior fossa ependymoma · progesterone-receptor negative breast cancer · prostate cancer · refractory malignant neoplasm · salivary gland cancer · small cell lung carcinoma · urethra cancer · urinary bladder cancer · uterine corpus cancer · acute myocardial infarction · bladder squamous cell carcinoma · breast ductal adenocarcinoma · carcinosarcoma of the corpus uteri · castration-resistant prostate carcinoma · central nervous system cancer · childhood acute myeloid leukemia · colorectal adenocarcinoma · colorectal carcinoma · digestive system cancer · digestive system neoplasm · ductal breast carcinoma in situ and lobular carcinoma in situ · endometrial clear cell adenocarcinoma · endometrial endometrioid adenocarcinoma · endometrial mixed adenocarcinoma · endometrial serous adenocarcinoma · endometrial undifferentiated carcinoma · endometrium adenocarcinoma · extrahepatic bile duct adenocarcinoma · gallbladder adenocarcinoma · gallbladder neoplasm · Hodgkins lymphoma · invasive lobular breast carcinoma · lung neoplasm · malignant colon neoplasm · malignant epithelial tumor of ovary · malignant leptomeningeal tumor · malignant tumor of meninges · malignant urinary system neoplasm · metastatic carcinoma · mycosis fungoides · myeloproliferative neoplasm · neoplasm of esophagus · nodal marginal zone B-cell lymphoma · oral cavity squamous cell carcinoma · osteosarcoma · ovarian neoplasm · pancreatic adenocarcinoma · pancreatic ductal adenocarcinoma · pancreatic large cell neuroendocrine carcinoma · pancreatic neoplasm · precursor lymphoblastic lymphoma/leukemia · prostate neoplasm · salivary duct carcinoma · salivary gland acinic cell carcinoma · salivary gland carcinoma · salivary gland mucoepidermoid carcinoma · skin neoplasm · soft tissue sarcoma · transitional cell carcinoma · triple-positive breast carcinoma · tumor of salivary gland · urinary bladder neoplasm · urothelial neoplasm · vulval Paget disease · central nervous system neoplasm
Investigated by
National Cancer Institute (NCI) · Hoffmann-La Roche · Genentech, Inc. · Fudan University · Novartis Pharmaceuticals · Dana-Farber Cancer Institute
+464 more · GlaxoSmithKline · Memorial Sloan Kettering Cancer Center · Pfizer · Sanofi · Eli Lilly and Company · Seagen Inc. · Novartis · Roche Pharma AG · AstraZeneca · Bristol-Myers Squibb · M.D. Anderson Cancer Center · SCRI Development Innovations, LLC · UNICANCER · Brigham and Women's Hospital · City of Hope Medical Center · Jiangsu HengRui Medicine Co., Ltd. · Massachusetts General Hospital · Merck Sharp & Dohme LLC · NSABP Foundation Inc · Alliance for Clinical Trials in Oncology · Beth Israel Deaconess Medical Center · Eisai Inc. · European Organisation for Research and Treatment of Cancer - EORTC · GBG Forschungs GmbH · NYU Langone Health · Puma Biotechnology, Inc. · SOLTI Breast Cancer Research Group · Spanish Breast Cancer Research Group · Translational Breast Cancer Research Consortium · UNC Lineberger Comprehensive Cancer Center · Washington University School of Medicine · Amgen · Aventis Pharmaceuticals · Chinese Academy of Medical Sciences · H. Lee Moffitt Cancer Center and Research Institute · Henan Cancer Hospital · Institut Curie · Jonsson Comprehensive Cancer Center · NRG Oncology · SWOG Cancer Research Network · The Netherlands Cancer Institute · West German Study Group · Asan Medical Center · Breast International Group · Cancer Research UK · Celgene Corporation · Daiichi Sankyo · Fate Therapeutics · Guangdong Provincial People's Hospital · Mayo Clinic · MedSIR · Pfizer · Samsung Medical Center · Shanghai Jiao Tong University School of Medicine · Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Susan G. Komen Breast Cancer Foundation · Tianjin Medical University Cancer Institute and Hospital · University Hospital of Crete · University of California, Irvine · University of Washington · Yale University · Yonsei University · Aarhus University Hospital · Academic Medical Center - University of Amsterdam · Bayer · Boehringer Ingelheim · Breast Cancer Research Foundation · Canadian Cancer Trials Group · Cancer Trials Ireland · Case Comprehensive Cancer Center · Cephalon · First Affiliated Hospital of Zhejiang University · Hellenic Oncology Research Group · all 470 on the full record

Regulatory milestones approvals, filings & regulatory actions · 12 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Label expansion US (FDA) PHESGO 2024-11-22 fda.gov
Label expansion US (FDA) HERCEPTIN HYLECTA 2024-06-18 fda.gov
Label expansion US (FDA) HERZUMA 2019-05-16 fda.gov
Label expansions (7) US (FDA) HERCEPTIN 2001-12-11 – 2014-03-07 fda.gov
Approved EU (EMA) Herceptin 2000-08-28 europa.eu
Approved US (FDA) HERCEPTIN 1998-09-25 fda.gov

Trials 686 · started per year

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EU approved 2000
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19971998199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020212022202320242025202620272028
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 07 trials
Phase 0 NCT06098898 Nov 2023 → Nov 2024 gastric cancer Base Therapeutics (Shanghai) Co., Ltd. Unknown No outcome recorded
Phase 0 NCT05238831 Jan 2023 → May 2026 female breast carcinoma, ovarian carcinoma, pancreatic ductal adenocarcinoma, pancreatic large cell neuroendocrine carcinoma +2 OHSU Knight Cancer Institute Withdrawn No outcome recorded
Phase 0 NCT04958486 Jul 2021 → Sep 2023 posterior fossa ependymoma The University of Texas Health Science Center, Houston Completed No outcome recorded
Phase 0 NCT04102618 Mar 2019 → Apr 2022 breast cancer Oncolytics Biotech Terminated No outcome recorded
Phase 0 NCT03321045 Nov 2017 → Oct 2028 expected breast cancer University of Alabama at Birmingham Recruiting No outcome recorded
Phase 0 NCT02735798 Apr 2016 → Jun 2017 metastatic malignant neoplasm in the brain Pamela Munster Withdrawn No outcome recorded
Phase 0 NCT00949247 Dec 2009 → Jan 2013 breast cancer Case Comprehensive Cancer Center Completed No outcome recorded
Phase 169 trials
Phase 1 NCT07299955 Feb → Jun 2026 overdue Biocon Biologics UK Ltd Recruiting No outcome recorded
Phase 1 NCT07216105 Nov 2025 → Jan 2028 expected breast cancer, colorectal cancer, endometrial carcinoma, head and neck squamous cell carcinoma +2 Fate Therapeutics Recruiting No outcome recorded
Phase 1 NCT05733689 Jun 2025 → Jun 2027 expected gastroesophageal adenocarcinoma University of California, Irvine Recruiting No outcome recorded
Phase 1 NCT05553522 Jan 2024 → Dec 2025 HER2 positive breast carcinoma, metastatic malignant neoplasm in the brain Baptist Health South Florida Terminated No outcome recorded
Phase 1 NCT06886659 Jan → Dec 2024 breast cancer Incepta Pharmaceuticals Ltd Completed No outcome recorded
Phase 1 NCT06162559 Dec 2023 → Aug 2026 overdue breast cancer The Netherlands Cancer Institute Recruiting No outcome recorded
Phase 1 NCT05187182 Jun 2023 → Jul 2028 expected esophageal cancer, gastric cancer, gastroesophageal cancer Washington University School of Medicine Recruiting No outcome recorded
Phase 1 NCT05395052 May 2022 → Aug 2023 breast cancer, colorectal cancer, gastroesophageal cancer, head and neck cancer +3 Fate Therapeutics Terminated No outcome recorded
Phase 1 NCT05378464 May 2022 → Aug 2026 HER2 positive breast carcinoma H. Lee Moffitt Cancer Center and Research Institute Suspended No outcome recorded
Phase 1 NCT05275010 May 2022 → May 2023 Hoffmann-La Roche Completed No outcome recorded
Phase 1/265 trials
Phase 1/2 NCT06027983 Nov → Dec 2026 expected HER2 positive breast carcinoma National University Hospital, Singapore Not yet recruiting No outcome recorded
Phase 1/2 NCT07136428 Jul 2026 → Nov 2030 expected HER2 positive breast carcinoma Duke University Not yet recruiting No outcome recorded
Phase 1/2 NCT07612215 May 2026 → May 2029 expected triple-positive breast carcinoma NYU Langone Health Recruiting No outcome recorded
Phase 1/2 NCT07140393 Oct 2025 → Oct 2027 expected neoplasm Jiangsu HengRui Medicine Co., Ltd. Recruiting No outcome recorded
Phase 1/2 NCT06686394 Feb 2025 → Apr 2030 expected breast cancer Merck Sharp & Dohme LLC Recruiting No outcome recorded
Phase 1/2 NCT06572319 Sep 2024 → Aug 2026 overdue gastroesophageal junction adenocarcinoma Zhejiang Cancer Hospital Recruiting No outcome recorded
Phase 1/2 NCT06650332 Jul 2024 → Aug 2026 overdue gastroesophageal cancer Zhejiang Cancer Hospital Recruiting No outcome recorded
Phase 1/2 NCT05785741 Aug 2023 → Dec 2027 expected neoplasm DualityBio Inc. Recruiting No outcome recorded
Phase 1/2 NCT05749900 May 2023 → Feb 2026 overdue Yonsei University Recruiting No outcome recorded
Phase 1/2 NCT05640830 Jan 2023 → Dec 2025 overdue carcinoma Kangbuk Samsung Hospital Recruiting No outcome recorded
Phase 2416 trials
Phase 2 NCT07694986 Aug 2026 → Aug 2029 expected breast cancer, neoplastic meningitis H. Lee Moffitt Cancer Center and Research Institute Recruiting No outcome recorded
Phase 2 NCT07565324 Apr 2026 → Dec 2029 expected HER2 positive breast carcinoma National Taiwan University Hospital Not yet recruiting No outcome recorded
Phase 2 NCT07402473 Mar 2026 → Dec 2027 expected HER2 positive breast carcinoma Rutgers, The State University of New Jersey Recruiting No outcome recorded
Phase 2 NCT07647263 Mar 2026 → Jun 2029 expected HER2 positive breast carcinoma The First Affiliated Hospital of Soochow University Recruiting No outcome recorded
Phase 2 NCT07393425 Feb 2026 → Sep 2027 expected HER2 positive breast carcinoma Shanghai Jiao Tong University School of Medicine Recruiting No outcome recorded
Phase 2 NCT07193394 Jan 2026 → Dec 2028 expected Her2-receptor negative breast cancer Institut Curie Recruiting No outcome recorded
Phase 2 NCT07290166 Dec 2025 → Oct 2027 expected breast cancer Fudan University Not yet recruiting No outcome recorded
Phase 2 NCT07340398 Dec 2025 → Dec 2028 expected HER2 positive breast carcinoma Second Affiliated Hospital, School of Medicine, Zhejiang University Recruiting No outcome recorded
Phase 2 NCT07299890 Dec 2025 → Nov 2027 expected breast cancer Anhui Provincial Cancer Hospital Not yet recruiting No outcome recorded
Phase 2 NCT07300215 Dec 2025 → Nov 2027 expected breast cancer The First Affiliated Hospital of Bengbu Medical University Not yet recruiting No outcome recorded
Show all 416 trials opens the full record — a long page
Phase 2/311 trials
Phase 2/3 NCT07000253 Apr 2026 → Jun 2031 expected carcinoma of esophagus, gastric adenocarcinoma Academic Medical Center - University of Amsterdam Recruiting No outcome recorded
Phase 2/3 NCT07366840 Jan 2026 → Jan 2028 expected HER2 positive breast carcinoma Fudan University Not yet recruiting No outcome recorded
Phase 2/3 NCT07332533 Dec 2025 → Jun 2032 expected carcinoma Shanghai JMT-Bio Inc. Not yet recruiting No outcome recorded
Phase 2/3 NCT05980481 Aug 2023 → Jul 2025 overdue gastric cancer RemeGen Co., Ltd. Active not recruiting No outcome recorded
Phase 2/3 NCT05786716 Mar 2023 → Oct 2029 expected cancer, colorectal neoplasm, gallbladder neoplasm, hematopoietic and lymphoid cell neoplasm +7 Cancer Research UK Recruiting No outcome recorded
Phase 2/3 NCT05722886 Mar 2023 → Oct 2029 expected cancer, hematopoietic and lymphoid cell neoplasm Cancer Research UK Recruiting No outcome recorded
Phase 2/3 NCT05002127 Jan 2022 → May 2024 overdue gastric adenocarcinoma, gastroesophageal junction adenocarcinoma ALX Oncology Inc. Active not recruiting No outcome recorded
Phase 2/3 NCT04499924 Mar 2021 → Apr 2024 esophageal adenocarcinoma, gastric adenocarcinoma, gastroesophageal junction adenocarcinoma Seagen Inc. Completed No outcome recorded
Phase 2/3 NCT03085368 Mar 2017 → May 2018 HER2 positive breast carcinoma Peking Union Medical College Hospital Unknown No outcome recorded
Phase 2/3 NCT02581462 Jun 2016 → Jul 2020 gastric cancer, gastroesophageal junction adenocarcinoma Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest Completed No outcome recorded
Phase 388 trials
Phase 3 NCT07683754 Sep 2026 → Jul 2030 expected HER2 positive breast carcinoma, female breast carcinoma, hormone receptor-positive breast cancer Daiichi Sankyo Not yet recruiting No outcome recorded
Phase 3 NCT06876714 Sep 2025 → Mar 2028 expected HER2 positive breast carcinoma Alliance for Clinical Trials in Oncology Recruiting No outcome recorded
Phase 3 NCT06992882 Jul 2025 → Jun 2028 expected HER2 positive breast carcinoma Fudan University Recruiting No outcome recorded
Phase 3 NCT06731478 Feb 2025 → Jun 2028 expected gastric cancer, gastroesophageal junction adenocarcinoma Daiichi Sankyo Recruiting No outcome recorded
Phase 3 NCT06490536 Oct 2024 → Mar 2026 overdue colorectal cancer IFOM ETS - The AIRC Institute of Molecular Oncology Recruiting No outcome recorded
Phase 3 NCT05615818 Jul 2024 → Jun 2027 expected biliary tract neoplasm UNICANCER Recruiting No outcome recorded
Phase 3 NCT06278870 Sep 2023 → Jun 2031 expected HER2 positive breast carcinoma Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University Recruiting No outcome recorded
Phase 3 NCT07062263 Jul 2023 → Jul 2029 expected HER2 positive breast carcinoma, biliary tract cancer Tata Memorial Centre Recruiting No outcome recorded
Phase 3 NCT05883852 Jun 2023 → Jul 2031 expected HER2 positive breast carcinoma Fudan University Recruiting No outcome recorded
Phase 3 NCT05388500 Dec 2022 → Dec 2030 expected HER2 positive breast carcinoma Institut de cancérologie Strasbourg Europe Not yet recruiting No outcome recorded
Phase 411 trials
Phase 4 NCT07695259 May 2026 → Dec 2027 expected HER2 positive breast carcinoma Wen-Ming Cao Recruiting No outcome recorded
Phase 4 NCT06217185 Jan 2024 → Dec 2025 overdue HER2 positive breast carcinoma Hebei Medical University Fourth Hospital Recruiting No outcome recorded
Phase 4 NCT06031233 Sep 2023 → Jul 2028 expected Isala Recruiting No outcome recorded
Phase 4 NCT04928261 Dec 2021 → Dec 2025 overdue breast cancer Ottawa Hospital Research Institute Active not recruiting No outcome recorded
Phase 4 NCT05036005 Jul 2021 → Apr 2023 HER2 positive breast carcinoma, female breast carcinoma Institut fuer Frauengesundheit Unknown No outcome recorded
Phase 4 NCT02419742 Aug 2015 → Jun 2021 breast cancer Hoffmann-La Roche Completed No outcome recorded
Phase 4 NCT02380131 Feb 2013 → Dec 2017 gastroesophageal adenocarcinoma Hebei Medical University Unknown No outcome recorded
Phase 4 NCT01260194 Jun 2011 → Jan 2015 gastric cancer Hoffmann-La Roche Terminated No outcome recorded
Phase 4 NCT01301729 Mar 2011 → Jul 2014 breast cancer Hoffmann-La Roche Completed No outcome recorded
Phase 4 NCT00127933 Aug 2005 → Apr 2009 breast cancer Hoffmann-La Roche Completed No outcome recorded
Phase not applicable17 trials
NCT07589972 Apr 2026 → Dec 2027 expected breast carcinoma by gene expression profile Tianjin Medical University Cancer Institute and Hospital Not yet recruiting No outcome recorded
NCT07187752 Sep 2025 → Dec 2026 expected breast cancer Shandong Cancer Hospital and Institute Not yet recruiting No outcome recorded
NCT07095023 Aug 2025 → Dec 2026 expected breast cancer Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University Recruiting No outcome recorded
NCT06854523 Apr 2025 → Dec 2026 expected acute myocardial infarction Yun Dai Chen Not yet recruiting No outcome recorded
NCT06035679 Aug 2023 → Nov 2026 expected female breast carcinoma Youzhi Zhu Recruiting No outcome recorded
NCT05656079 Jul 2021 → Sep 2024 breast cancer Shanghai Pudong Hospital Unknown No outcome recorded
NCT06907082 Dec 2020 → Mar 2024 breast cancer Fundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia Completed No outcome recorded
NCT03947242 Jun 2019 → Jun 2020 HER2 positive breast carcinoma Henan Cancer Hospital Unknown No outcome recorded
NCT03847818 Mar 2019 → Mar 2020 HER2 positive breast carcinoma Shandong University Unknown No outcome recorded
NCT02563925 Sep 2015 → Jul 2021 breast cancer Memorial Sloan Kettering Cancer Center Completed No outcome recorded
Phase not stated2 trials
NCT04220203 HER2 positive breast carcinoma Pfizer Approved for marketing No outcome recorded
NCT04395508 HER2 positive breast carcinoma Genentech, Inc. Approved for marketing No outcome recorded
Also used as a comparator or background therapy in 343 trials
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 02 trials
Phase 0 NCT03387553 Background Jun 2018 → Aug 2023 HER2 positive breast carcinoma, female breast carcinoma, invasive breast carcinoma, male breast carcinoma H. Lee Moffitt Cancer Center and Research Institute Completed No outcome recorded
Phase 0 NCT01875666 Comparator Aug 2013 → Dec 2016 breast neoplasm UNC Lineberger Comprehensive Cancer Center Completed No outcome recorded
Phase 155 trials
Phase 1 NCT06687928 Comparator Mar → Aug 2025 Celltrion Completed No outcome recorded
Phase 1 NCT06770296 Background Nov 2024 → Nov 2026 expected breast cancer The First Affiliated Hospital with Nanjing Medical University Recruiting No outcome recorded
Phase 1 NCT06625775 Background Oct 2024 → Nov 2028 expected HER2 positive breast carcinoma, colorectal cancer, hormone receptor-positive breast cancer, lung carcinoma TheRas, Inc., d/b/a BBOT (BridgeBio Oncology Therapeutics) Recruiting No outcome recorded
Phase 1 NCT06328738 Background May 2024 → Jan 2027 expected HER2 positive breast carcinoma, colorectal cancer Enliven Therapeutics Active not recruiting No outcome recorded
Phase 1 NCT06253871 Background Mar 2024 → Dec 2027 expected HER2 positive breast carcinoma, gastroesophageal cancer, metastatic malignant neoplasm in the brain, non-small cell lung carcinoma +1 Iambic Therapeutics, Inc Recruiting No outcome recorded
Phase 1/233 trials
Phase 1/2 NCT07040059 Comparator Mar → Dec 2025 gastroesophageal junction adenocarcinoma Aurigene Discovery Technologies Limited Terminated No outcome recorded
Phase 1/2 NCT06771622 Background Mar 2025 → Jan 2028 expected FBD Biologics Limited Active not recruiting No outcome recorded
Phase 1/2 NCT06324357 Background Jun 2024 → Jan 2029 expected breast cancer, colorectal cancer, esophageal adenocarcinoma, gastric adenocarcinoma +1 Boehringer Ingelheim Recruiting No outcome recorded
Phase 1/2 NCT07334431 Background Feb 2024 → Dec 2025 overdue gastric adenocarcinoma, gastroesophageal junction adenocarcinoma Henan Cancer Hospital Recruiting No outcome recorded
Phase 1/2 NCT05256745 Background Jun 2023 → Dec 2026 expected breast cancer, subjective cognitive decline Georgetown University Recruiting No outcome recorded
Phase 2122 trials
Phase 2 NCT07679269 Background Jan 2027 → Jun 2031 expected PIK3CA-related overgrowth spectrum, breast neoplasm Novartis Pharmaceuticals Not yet recruiting No outcome recorded
Phase 2 NCT07610720 Background Jun 2026 → Nov 2028 expected HER2 positive breast carcinoma Sun Yat-sen University Recruiting No outcome recorded
Phase 2 NCT07581795 Background Jun 2026 → Feb 2029 expected HER2 positive breast carcinoma Fudan University Not yet recruiting No outcome recorded
Phase 2 NCT07545044 Comparator May 2026 → May 2027 expected HER2 positive breast carcinoma Shanghai JMT-Bio Inc. Not yet recruiting No outcome recorded
Phase 2 NCT07616427 Background May 2026 → May 2028 expected HER2 positive breast carcinoma Second Affiliated Hospital, School of Medicine, Zhejiang University Recruiting No outcome recorded
Show all 122 trials opens the full record — a long page
Phase 2/313 trials
Phase 2/3 NCT07413939 Background May 2026 → May 2029 expected HER2 positive breast carcinoma Hoffmann-La Roche Recruiting No outcome recorded
Phase 2/3 NCT07294508 Comparator Feb 2026 → Jan 2028 expected HER2 positive breast carcinoma Shanghai Henlius Biotech Recruiting No outcome recorded
Phase 2/3 NCT07294534 Comparator Jan 2026 → Sep 2028 expected HER2 positive breast carcinoma Shanghai Henlius Biotech Not yet recruiting No outcome recorded
Phase 2/3 NCT06504732 Comparator Aug 2024 → Jul 2028 expected gastric neoplasm SUNHO(China)BioPharmaceutical CO., Ltd. Recruiting No outcome recorded
Phase 2/3 NCT05426486 Comparator May 2022 → Dec 2025 overdue HER2 positive breast carcinoma Caigang Liu Active not recruiting No outcome recorded
Phase 3101 trials
Phase 3 NCT07578116 Background Mar 2027 → May 2032 expected HER2 positive breast carcinoma, female breast carcinoma SWOG Cancer Research Network Not yet recruiting No outcome recorded
Phase 3 NCT07508956 Background Jun 2026 → Mar 2029 expected gastroesophageal adenocarcinoma Shanghai Zhongshan Hospital Not yet recruiting No outcome recorded
Phase 3 NCT07528716 Background May 2026 → Dec 2027 expected breast cancer Fudan University Recruiting No outcome recorded
Phase 3 NCT07518173 Comparator Apr 2026 → Dec 2029 expected HER2 positive breast carcinoma Sichuan Baili Pharmaceutical Co., Ltd. Recruiting No outcome recorded
Phase 3 NCT07441460 Comparator Mar 2026 → Aug 2034 expected HER2 positive breast carcinoma Shanghai JMT-Bio Inc. Recruiting No outcome recorded
Phase 46 trials
Phase 4 NCT07093931 Background Aug 2025 → Aug 2027 expected breast cancer Shandong Cancer Hospital and Institute Not yet recruiting No outcome recorded
Phase 4 NCT05376878 Background Dec 2022 → Apr 2027 expected invasive breast carcinoma, metastatic malignant neoplasm in the brain City of Hope Medical Center Recruiting No outcome recorded
Phase 4 NCT05420454 Background Jul 2022 → Jun 2027 expected breast cancer Second Affiliated Hospital, School of Medicine, Zhejiang University Recruiting No outcome recorded
Phase 4 NCT05420467 Background Jul 2022 → Jul 2027 expected breast cancer Second Affiliated Hospital, School of Medicine, Zhejiang University Recruiting No outcome recorded
Phase 4 NCT02445586 Background Aug 2015 → Sep 2018 breast cancer Hoffmann-La Roche Completed No outcome recorded
Phase not applicable11 trials
NCT07115095 Background Jan 2021 → Jan 2023 HER2 positive breast carcinoma Nanlin Li Completed No outcome recorded
NCT04281576 Background Dec 2019 → Jun 2024 gastric cancer, gastroesophageal cancer NovoCure Ltd. Completed No outcome recorded
NCT03756064 Background Aug 2019 → Jul 2020 breast cancer Zhejiang Cancer Hospital Unknown No outcome recorded
NCT03843749 Background Jul 2019 colorectal cancer Shanghai Changzheng Hospital Unknown No outcome recorded
NCT06190600 Background Oct 2018 → Mar 2020 overdue female breast carcinoma The Greater Poland Cancer Centre Active not recruiting No outcome recorded

Press releases naming this drug 66 releases

DateIssuerRelease
2023-09-18 Novartis Pharmaceuticals Sandoz receives positive CHMP opinion for breast and gastric cancer biosimilar trastuzumab novartis.com
2021-12-22 Novartis Pharmaceuticals Sandoz submits Marketing Authorization Application for proposed biosimilar trastuzumab to EMA novartis.com
2021-12-20 Novartis Pharmaceuticals Sandoz submits Biologics License Application for proposed biosimilar trastuzumab to US FDA novartis.com
2020-12-23 Roche Global Development European Commission approves Roche’s Phesgo (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection) for people with HER2-positive breast cancer roche.com
2020-12-14 Daiichi Sankyo Trastuzumab Deruxtecan Recommended for Approval in the EU by CHMP for HER2 Positive Metastatic Breast Cancer daiichisankyo.com
2020-11-13 Roche Global Development CHMP recommends EU approval of Roche’s Phesgo (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection) for HER2-positive breast cancer roche.com
2020-07-07 Daiichi Sankyo EMA Validates and Grants Accelerated Assessment for Trastuzumab Deruxtecan for the Treatment of HER2 Positive Metastatic Breast Cancer daiichisankyo.com
2020-06-29 Roche Global Development FDA approves Roche’s Phesgo (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection) for HER2-positive breast cancer roche.com
2020-05-07 Daiichi Sankyo Daiichi Sankyo Submits Supplemental New Drug Application for Trastuzumab Deruxtecan in Japan for Treatment of Patients with HER2 Positive Metastatic Gastric Cancer daiichisankyo.com
2020-03-16 Teva Branded Pharmaceutical Products R&D, Inc. Teva and Celltrion Healthcare Announce U.S. Availability of HERZUMA® (trastuzumab-pkrb) for Injection tevapharm.com
2020-02-25 Roche Global Development FDA accepts Roche’s Biologics License Application for fixed-dose subcutaneous combination of Perjeta and Herceptin for HER2-positive breast cancer roche.com
2019-12-12 Roche Global Development Roche’s fixed-dose subcutaneous combination of Perjeta and Herceptin comparable to intravenous formulations in people with HER2-positive breast cancer roche.com

Evidence & citations 35 cited values

Every value below carries the sentence it was read from. 1,037 sources stand behind the page.

FieldValueCited text
Known as trastuzumab “Patients with measurable/evaluable HER2-positive LR/MBC who had not received trastuzumab or chemotherapy for LR/MBC were stratified by prior adjuvant trastuzumab, prior...” PMID 23569311 Apr 2013
953

“Patient must have received continuous anti-HER2 targeted therapy (including Trastuzumab, Trastuzumab/Pertuzumab, Trastuzumab-Deruxtecan, T-DM1) for at least 2 years in any line...” NCT06450314

“This first-in-human study with SB3 was designed to evaluate the pharmacokinetic (PK) equivalence between SB3 and trastuzumab sourced in the European Union (EU trastuzumab),...” PMID 27368117 Jun 2016

“In this study, the investigators plan multicenter phase II clinical trial to test the efficacy, safety and immunogenicity of trastuzumab biosimilar, Herzuma® in combination...” NCT03755141

“In patients with ER-positive and HER2-positive breast cancer, the therapeutic potential of combining trastuzumab, pertuzumab, and pyrotinib-representing a triple-targeted...” NCT07290166

“IAM1363 monotherapy OR IAM1363 in combination with capecitabine + trastuzumab OR IAM1363 in combination with capecitabine + zanidatamab OR IAM1363 in combination with T-Dxd OR...” NCT06253871

Trastuzumab 8 mg/kg will be administered as in IV infusion over a 90-minute period on Day 1 of Cycle 1. Thereafter, trastuzumab 6 mg/kg will be administered as an IV infusion...” NCT01269346

“Patients received neoadjuvant chemotherapy consisting of paclitaxel (80 mg/m2, day 1 and 8 of each 21-day cycle, intravenous), trastuzumab (6 mg/kg on day 1 of each cycle...” PMID 41713473 Feb 2026

“Patients, for whom concurrent HER2 directed therapy trastuzumab is indicated, as determined by the treating investigator, will be enrolled in a parallel HER2 directed therapy...” NCT02563925

“Phase I/II Clinical Study of the Combination of Disitamab Vedotin and Trastuzumab in the Treatment of HER2 Positive Gastric/Gastroesophageal Junction Tumors With Previous...” NCT06572319

“Neoadjuvant Trastuzumab and Pertuzumab Plus Endocrine Therapy Versus Chemotherapy in Hormone Receptor-Positive/Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer” PMID 42150145 May 2026

Trastuzumab 4 mg/kg loading dose on Day 1 of the first cycle, then 2 mg/kg on Days 8 and 15 of the first cycle and on Days 1, 8, and 15 of the subsequent cycles, every 3 weeks” NCT01669239

“capecitabine (1000-1250mg/m2, orally, bid, D1-14, q3w) and trastuzumab (first dose 8mg/kg, q3w; Follow-up maintenance 6 mg/kg, q3w, subcutaneous or intravenous for 1 year)” NCT06992882

Trastuzumab plus docetaxel was chosen as the comparator in the control group,as it represents a common first-line treatment option used in HER2+ MBC population in China.” NCT04385563

“Single dose group: lyophilized powder of Trastuzumab Injection; strength 440 mg/bottle; 6 mg/kg for one dose, intravenous infusion, completed for over 90 minutes” NCT04170595

Trastuzumab (8mg/kg first dose, 6mg/kg sequential) and Patuzumab (840mg first dose, 420mg/kg sequential) were administered intravenously every 3 weeks” NCT06276868

“Lapatinib in combination with paclitaxel, letrozole, capecitabine, capecitabine/oxaliplatin, gemcitabine, docetaxel, trastuzumab, FOLFOX4, or FOLFIRI” NCT00790816

“Patients with HER2-neu positive breast cancer, will receive the same chemotherapy in combination with intravenous (iv) Herceptin (trastuzumab).” NCT00127933

“A phase I trial of escalating doses of trastuzumab combined with daily subcutaneous interleukin 2: report of cancer and leukemia group B 9661.” PMID 12473581 Dec 2002

“Docetaxel, carboplatin, trastuzumab, and pertuzumab (TCHP)for 6 cycles, administered per USPI (Unites States Prescribing Information) Label” NCT05256745

“with (for patients with positive HER-2) or without Trastuzumab (loading dose of 6 mg/kg followed by 4 mg/kg every 2 weeks for four cycles)” NCT03242551

“According to the results of the genetic mutation status, HER2-positive patients are administered trastuzumab in combination every cycle.” NCT07655024

“TCH-P Taxotere (docetaxel), Carboplatin, Herceptin (trastuzumab), Perjeta (pertuzumab) standard of care neoadjuvant chemotherapy regimen” NCT03387553

“The primary amino acid sequences of trastuzumab in CT-P6 SC are identical to those of the reference drug (EU-approved Herceptin SC).” NCT06687928

Trastuzumab will be administered concurrently with any anthracycline-containing regimen for breast cancer adjuvant chemotherapy.” NCT01413828

Trastuzumab (only for HER2-positive patients): Loading dose: 8 mg/kg, Maintenance dose: 6 mg/kg, day 1 q day 22 for 6 cycles.” NCT01426880

Trastuzumab: initial loading dose 8 mg/kg, maintenance dose 6 mg/kg, intravenous infusion, administered once every 3 weeks.” NCT07589972

“FOLFOX plus anti-HER2 antibody trastuzumab as a second-line or third-line treatment for HER2-positive biliary tract cancer.” PMID 36328033 Oct 2022

Trastuzumab initial dose of 4 mg/kg over 90 minute IV infusion, then 2 mg/kg over 30 minute IV infusion weekly for 52 weeks” NCT01501487

“Pyrotinib combined with docetaxel, carboplatin and trastuzumab (TCbHPy) for neoadjuvant therapy of HR+/HER2+ breast cancer” NCT05430347

Trastuzumab 4 mg/kg iv wk 1 → Trastuzumab 2 mg/kg iv for 17 wks → Trastuzumab 6 mg/kg iv every 3 wks to complete 1 year” NCT01917578

“Drug: Trastuzumab Trastuzumab 8mg/kg \[loading dose\] once then 6mg/kg IV every 21 days for 3 cycles plus docetaxel.” NCT01472146

“the neoadjuvant treatment regimen of trastuzumab dual-target combined with exemestane and palbociclib for 4 cycles.” NCT07300215

“EirGenix' Trastuzumab and Herceptin® (Trastuzumab) Sourced From US and EU Administered to Healthy Male Volunteers” NCT03180242

Trastuzumab 8 mg/kg loading dose iv on day 2, followed by 6 mg/kg iv on day 2 of each subsequent 3 weekly cycle” NCT02411344

“The patient used Trastuzumab 150mg within 24 hours before or after PCI, and then every two weeks for 12 months” NCT06854523

Trastuzumab: 4mg/kg IV load dose (TRO 90) minutes followed by 2 mg/kg TRO 60 minutes every week for 18 weeks” NCT01163929

Trastuzumab: 8mg/Kg in the first cycle, 6mg/Kg in the subsequent cycle, intravenous(iv), every 3 weeks(q3w)” NCT06254690

Trastuzumab: 8mg/Kg in the first cycle, 6mg/Kg in the subsequent cycle, intravenous(iv), every 3 weeks(q3w)” NCT06770296

“include Trastuzumab (Herceptin) as part of the neoadjuvant treatment in patients who are Her-2 positive.” NCT00830544

“sequence of Trastuzumab,pyrotinib and Nab-Paclitaxel in first line followed by SHR-A1811 in second line” NCT06975475

“for HER-2 positive patients: trastuzumab loading dose 4mg/kg, then 2mg/kg, day 1, 8, 15, 22, q4w.” NCT01625429

“RATIONALE: Monoclonal antibodies, such as trastuzumab, can block tumor growth in different ways.” NCT00943410

Trastuzumab: 8 mg/kg i.v. loading dose on day 1, followed by 6 mg/kg i.v.infusion every 3 weeks” NCT01396707

trastuzumab 8 mg/kg loading, then 6 mg/kg, pertuzumab 840 mg loading, then 420 mg, iv, q3w” NCT05346107

“combined with subcutaneous (SC) fixed dose combination (FDC) of pertuzumab and trastuzumabNCT04675827

“CDK 4/6 inhibitor and endocrine therapy combined with Trastuzumab ( without chemotherapy)” NCT07213206

Trastuzumab Biosimilar (Herzuma®) in Patients with HER2 Mutated Advanced Solid Cancers” NCT06083662

“Prior to surgery: trastuzumab, HS627, and docetaxel for 4 cycles (1 cycle = 21 days).” NCT04514419

“Monoclonal antibodies, such as trastuzumab, can block tumor growth in different ways.” NCT00118053

“Monoclonal antibodies, such as trastuzumab, can block tumor growth in different ways.” NCT00138125

“HER2-Positive: Trastuzumab combined with chemotherapy, with or without immunotherapy.” NCT07257380

“Targeted therapy: trastuzumab (HER2-positive) or zolbetuximab (Claudin 18.2-positive)” NCT07000253

“HER2-Positive: Trastuzumab combined with chemotherapy, with or without immunotherapy.” NCT07508956

Trastuzumab was administered at 2 mg/kg weekly after a loading dose of 4 mg/kg.” PMID 20705560 Aug 2010

“containing 15 mL solution of 1200 mg of pertuzumab and 600 mg of trastuzumab.” NCT06172127

“nab-paclitaxel + carboplatin + trastuzumab + pertuzumab (PCbHP, control arm)” NCT07528716

Trastuzumab (iv) will be administered as weekly use or tri-weekly use.” NCT01432886

trastuzumab (8 mg/kg loading dose followed by 6 mg/kg Q3W on Day 1)” NCT06548178

“Paclitaxel, and Trastuzumab in Patients With Operable Breast Cancer” NCT00518583

“Herceptin® (US-licensed Trastuzumab and EU-licensed Trastuzumab)” NCT03242239

“Pertuzumab + Trastuzumab + Taxane (docetaxel or paclitaxel)” NCT06135714

“All participants will received trastuzumab and pertuzumab.” NCT04750122

“pyrotinib combined with trastuzumab and albumin paclitaxel” NCT05429294

“HER2-positive patients will also receive trastuzumab.” PMID 40953882 Sep 2025

“docetaxel, carboplatin, trastuzumab, and pertuzumab” NCT07239271

“Drug: Cetuximab Drug: Trastuzumab Drug: Gefitinib” NCT03768375

“Docetaxel +Carboplatin+Trastuzumab+Pertuzumab+” NCT07294534

Trastuzumab 6 mg/kg IV over 60 minutes day -14” NCT00617942

Trastuzumab 2mg/kg IV QW (first dose 4 mg/kg)” NCT03085368

“docetaxel/carboplatin/trastuzumab/Pertuzumab” NCT04094896

trastuzumab (6 mg/kg, loading dose 8 mg/kg)” NCT01996267

“Pyrotinib in Combination With TrastuzumabNCT03843749

“either avelumab, trastuzumab or cetuximab” NCT05069935

Trastuzumab 6mg/kg(initial dose 8mg/kg)” NCT05871918

trastuzumab reference product (TRZ)” PMID 29448072 Feb 2018

“Pertuzumab+ Trastuzumab+Docetaxel” NCT07294508

Trastuzumab 40 mg/m2,po bid” NCT06036745

“* Trastuzumab (600mg, SC)” NCT03881878

“Biological: TrastuzumabNCT04034823

trastuzumab (Herceptin)” NCT00095706

trastuzumab, 8 cycles” NCT01206881

Trastuzumab * Dose:” NCT02226757

“Drug: TrastuzumabNCT06650332

Trastuzumab (T)” NCT03262935

TrastuzumabNCT02142036

NCT05318339

NCT05143970

NCT01472029

NCT01674062

NCT01275677

NCT01340430

NCT05346861

NCT04639271

NCT00088985

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NCT01364493

NCT05800275

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NCT04307329

NCT00427427

NCT01427244

NCT01810393

NCT04215159

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NCT00182793

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NCT00712140

NCT04789096

NCT07307287

NCT02091960

NCT05985187

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NCT02654119

NCT03994107

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NCT06731478

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NCT03847818

NCT03112590

NCT00821886

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NCT01816594

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NCT06190600

NCT07612215

NCT01205217

NCT03365882

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NCT05188313

NCT04309578

NCT04088110

NCT00243503

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NCT00533936

NCT02586025

NCT04819971

NCT01565083

NCT06625775

NCT04512261

NCT01402401

NCT06130007

NCT00364611

NCT03457896

NCT04419181

NCT06239467

NCT07441460

NCT00971737

NCT00629499

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NCT00006228

NCT03014076

NCT00912340

NCT00006825

NCT05187182

NCT00258960

NCT00820872

NCT01204372

NCT05800756

NCT02004769

NCT06730373

NCT01764022

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NCT07335081

NCT02448420

NCT00194779

NCT05189067

NCT06145308

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NCT01772472

NCT00134680

NCT02638428

NCT00428922

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NCT06832904

NCT01276041

NCT06771622

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NCT06589830

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NCT06439693

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NCT03498521

NCT06532006

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NCT03448042

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NCT06886659

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NCT03947242

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NCT02843126

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NCT00093808

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NCT04733118

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NCT00003995

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NCT07047365

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NCT04917900

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NCT04888663

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NCT05002127

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NCT02131064

NCT06121700

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NCT02213042

NCT00303108

NCT00005033

NCT07413939

NCT01235897

NCT00811993

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NCT06468280

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NCT07003074

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NCT01041404

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NCT06881017

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NCT05408845

NCT07407920

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NCT00103233

NCT06035679

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NCT04717531

NCT02726399

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NCT03101748

NCT02465060

NCT00550771

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NCT04236310

NCT00781612

NCT04900311

NCT01132664

NCT00434031

NCT05076695

NCT01730833

NCT01042925

NCT05228951

NCT00053339

NCT00006123

NCT03125928

NCT04499924

NCT06245356

NCT00085020

NCT01855828

NCT06907082

NCT02003209

NCT00392392

NCT03273595

NCT00667251

NCT01880385

NCT00036868

NCT04481932

NCT01387373

NCT00251433

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NCT03716180

NCT02214004

NCT05605509

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NCT02390427

NCT00077376

NCT02725424

NCT00717405

NCT02907918

NCT01104571

NCT07545044

NCT02260531

Known as Aryogen Trastuzumab “A Phase III, Randomized, Two-armed, Triple Blinded, Parallel, Active Controlled Non-Inferiority Clinical Trial of AryoTrust (AryoGen Trastuzumab) Efficacy and Safety in...” NCT03425656
Known as AryoTrust “Comparing Efficacy and Safety of AryoGen Pharmed Biosimilar Trastuzumab (AryoTrust) Versus Herceptin® in Breast Cancer” NCT03425656
Known as CT-P6 “Combination of pertuzumab and the trastuzumab biosimilar CT-P6 (Herzuma®) in Her2-positive breast cancer susceptible to neoadjuvant chemotherapy.” NCT06907082
2

NCT01084876

NCT01084863

Known as EU-Herceptin ClinicalTrials.gov intervention name — accepted as the source's own label NCT03776240
Known as FDC of Pertuzumab and Trastuzumab ClinicalTrials.gov intervention name — accepted as the source's own label NCT03493854
Known as H SC “BACKGROUND: This SafeHer subgroup analysis assessed the safety of fixed-dose subcutaneous trastuzumab (H SC) as an adjuvant therapy in HER2-positive early breast cancer (EBC)...” PMID 30018134 Jul 2018
Known as Hanquyou “Trastuzumab (Hanquyou): on the first day of the 21 day cycle, the initial dose was 8mg/kg” NCT05969184
Known as Her Herceptin™ (Her) loading dose 4 mg/kg iv, followed by 2 mg/kg iv weekly or loading dose 8 mg/kg iv, followed by 6 mg/kg iv every 3 weeks; at time of progression add chemotherapy” NCT00004935
Known as Herceptin “The AVEREL trial [A Study of Avastin (Bevacizumab) in Combination With Herceptin (Trastuzumab)/Docetaxel in Patients With HER2-Positive Metastatic Breast Cancer] evaluated...” PMID 23569311 Apr 2013
177

“This randomized, open-label, parallel, 2-arm, multicenter study will compare the administration of Herceptin (trastuzumab) with a single-use injection device versus a handheld...” NCT01344863

“Arm I (control arm, 12-month therapy): Patients continue to receive trastuzumab (Herceptin®) IV until a total of 12 months of therapy is completed in the absence of disease...” NCT00381901

“A Phase I/II Study of Suberoylanilide Hydroxamic Acid (SAHA) in Combination With Trastuzumab (Herceptin) in Patients With Advanced Metastatic and/or Local Chest Wall Recurrent...” NCT00258349

“Trastuzumab for injection is a biosimilar of Herceptin ® produced by Chia Tai Tianqing Biotechnology Co., LTD, which is a humanized IgG1 monoclonal antibody produced by chinese...” NCT05765357

“One is called trastuzumab (Herceptin®) and it is commonly given to women with early HER2 positive breast cancer or with advanced HER2 positive breast cancer that has spread to...” NCT01276041

“A Randomized Phase III Study of Trastuzumab (Herceptin) in Combination With Either Vinorelbine (Navelbine), or Taxane-based Chemotherapy in Patients With HER2 Overexpressing...” NCT00146549

“The purpose of the study is to investigate the effects (good and bad) that the combination of the drugs letrozole (also called Femara™) and trastuzumab (also called Herceptin®)...” NCT00134680

“A Study to Compare Subcutaneous (SC) Versus Intravenous (IV) Administration of Herceptin (Trastuzumab) in Women With Human Epidermal Growth Factor Receptor (HER) 2-Positive...” NCT00950300

“The drug, docetaxel, is combined with another drug, trastuzumab (Herceptin), because at this time this combination appears to be promising in metastatic breast cancer research.” NCT00146042

“Prospective Randomised Clinical Trial Testing the Role of Prophylactic Cranial Radiotherapy in Patients Treated With Trastuzumab (Herceptin®) for Metastatic Breast Cancer” NCT00639366

“Patients receive trastuzumab (Herceptin\^®) IV over 30-90 minutes on days 1, 8, 15, and 22 and docetaxel IV over 1 hour and carboplatin IV over 30-60 minutes on day 8.” NCT00118053

“Patients then receive paclitaxel IV over 60 minutes and trastuzumab (Herceptin®) IV over 90 minutes on days 1, 8, and 15 and oral lapatinib ditosylate on days 1-21.” NCT00436566

“Patients receive paclitaxel IV over 3 hours followed by carboplatin IV over 30 minutes and then trastuzumab (Herceptin) IV over 90 minutes on day 1 of week 1.” NCT00003612

“Patients receive trastuzumab (Herceptin) IV over 30-90 minutes on days 1, 8, and 15; paclitaxel IV over 3 hours on day 2; and oral capecitabine on days 3-16.” NCT00006108

“To evaluate if 3 months of trastuzumab (Herceptin®) administered according to the Finnish protocol (9-weekly administrations) is not inferior to 12 months” NCT00629278

“Those who are Her2+ will initially also receive TEC but subsequent therapy will include Trastuzumab(Herceptin) whether thet respond wellor not to TEC.” NCT01641406

“Phase II and Pharmacokinetic Study of CPT-11 and Trastuzumab (RhuMab HER2, Herceptin) in Advanced Colo-Rectal Cancer With p185 HER 2 Overexpression” NCT00003995

“characterize the pharmacokinetic, safety and immunogenicity of CMAB809 versus Trastuzumab(Herceptin) in healthy male subjects after a single dose.” NCT04049409

“OBJECTIVES: I. Assess the activity of trastuzumab (Herceptin) in patients with progressive androgen dependent and independent prostate cancer.” NCT00003740

“i.v. Trastuzumab (Herceptin®) and i.v. Paclitaxel as Treatment for Adult Female Patients With HER2 Overexpressing Metastatic Breast Cancer” NCT00788931

“Patients with HER-2/neu-positive tumors also receive trastuzumab (Herceptin®) IV over 90 minutes on day 1 of each course of chemotherapy” NCT00288002

“TCH-P Taxotere (docetaxel), Carboplatin, Herceptin (trastuzumab), Perjeta (pertuzumab) standard of care neoadjuvant chemotherapy regimen” NCT03387553

“Patients receive docetaxel IV over 30 minutes weekly for 6 weeks plus trastuzumab (Herceptin) IV over 30-90 minutes weekly for 8 weeks.” NCT00006104

Herceptin:Lyophilized powder of Trastuzumab Injection; strength 440 mg/bottle; 2mg/kg, the first infusion is completed over 90 minutes.” NCT04170595

“Patients receive trastuzumab (Herceptin) IV over 90 minutes on days 1, 8, 15, and 22 plus oral R115777 twice daily for 3 weeks.” NCT00005842

“Patients receive a loading dose of trastuzumab (Herceptin) IV over 90 minutes followed by paclitaxel IV over 3 hours on day 0.” NCT00005635

“Patients receive a loading dose of trastuzumab (Herceptin®) IV over 90 minutes on day 1 and over 30 minutes on days 8 and 15.” NCT00068757

“One is called trastuzumab (Herceptin) and it is commonly given to women with advanced and early HER2 positive breast cancer.” NCT02252887

“Patients then receive trastuzumab (Herceptin®) IV over 30-90 minutes and paclitaxel IV over 1 hour once a week for 12 weeks.” NCT00533936

“A Safety and Pharmacokinetic Study Between HLX02 and Herceptin®(U.S. and German Sourced) in Healthy Chinese Male Subjects” NCT02581748

“Patients receive trastuzumab (Herceptin) IV over 30-90 minutes followed by paclitaxel IV over 60 minutes on day 1.” NCT00009997

“in combination with trastuzumab (Herceptin®) in patient with non-resectable liver metastases from breast cancer.” NCT01387295

“versus Herceptin® (Trastuzumab-EU) approved in the EU in combination with Taxotere® and Carboplatin (Paraplatin)” NCT02187744

“Trastuzumab (INN; trade name Herceptin) is a monoclonal antibody that interferes with the HER2/neu receptor.” NCT00014430

“Trastuzumab (Herceptin ®): 6 mg/kg every 3 weeks (8 mg/kg as loading dose at 1st administration), iv, d1.” NCT03185988

“include Trastuzumab (Herceptin) as part of the neoadjuvant treatment in patients who are Her-2 positive.” NCT00830544

“Patients receive trastuzumab (Herceptin) IV over 30-90 minutes on day 1 and oral exemestane once daily.” NCT00057993

“Patients receive trastuzumab (Herceptin®) IV over 30-90 minutes once in weeks 1-3 OR once in week 1.” NCT00238290

“Patients also receive trastuzumab (Herceptin®) IV over 30-90 minutes once weekly beginning on day 1.” NCT00036868

“Patients continue or restart trastuzumab (Herceptin) IV over 30-90 minutes weekly or every 3 weeks.” NCT00006381

“combination of the proteasome inhibitor bortezomib (PS-341, Velcade) with trastuzumab (Herceptin)” NCT00199212

“irinotecan hydrochloride and trastuzumab (Herceptin®) after prior first- or second-line therapy” NCT00303992

“Patients are stratified according to prior treatment with trastuzumab (Herceptin®) (yes vs no)” NCT00107393

“Arm II: Patients receive trastuzumab (Herceptin) IV over 30-90 minutes weekly for 8 weeks.” NCT00005857

“Patients then receive docetaxel in week 13 and trastuzumab (Herceptin®) in weeks 13-15.” NCT00379015

Herceptin: 4 mg/kg (loading dose 8mg/kg) ivgtt d1,8,15, 22, 28 days per cycle,6 cycles.” NCT04215003

“Trastuzumab (Herceptin) is an FDA-approved treatment for HER2 positive breast cancer.” NCT02066532

“trastuzumab (Herceptin), docetaxel, and vinorelbine with filgrastim (G-CSF) support.” NCT00041067

“Trastuzumab (Herceptin®) is a recombinant DNA-derived humanized monoclonal antibody” NCT05385705

“trastuzumab (Herceptin) in the treatment of advanced or metastatic breast cancer.” NCT03085368

“Patients receive high-dose melphalan IV with or without trastuzumab (Herceptin®).” NCT00182793

“a drug called trastuzumab (also known as Herceptin®; Roche, Basel, Switzerland).” PMID 32880572 Aug 2020

“For patients with Her2 positive, add Herceptin 4mg/kg(6mg/kg first cycle) D1” NCT03691454

“paclitaxel, Herceptin® (trastuzumab), carboplatin, and pertuzumab (PTC-Ptz)” NCT03820063

“and plus Herceptin 2mg/kg qw, 6mg/kg q3w after chemotherapy until 1 year” NCT02934828

“trastuzumab (Herceptin®) IV over 30-90 minutes once weekly for 3 weeks” NCT00301730

“Patients receive trastuzumab (Herceptin) IV over 30-90 minutes weekly.” NCT00005033

“trastuzumab (Herceptin) IV over 30-90 minutes on days 1, 8, and 15.” NCT00006825

“Abraxane (nab-paclitaxel), Herceptin (trastuzumab) and carboplatin” NCT00617942

“trastuzumab [Herceptin] doses when administered with docetaxel” NCT01120184

“AC-PH (4+4) \[Adriamycin + Cytoxan + Paclitaxel + Herceptin\]” NCT02457039

“and HER-2 positive patients were added with Herceptin therapy” NCT04510064

“* Group A: Trastuzumab (Herceptin) + Vinorelbine (Navelbine)” NCT03414658

“subjects will receive a dose of trastuzumab (Herceptin®).” NCT00726180

“trastuzumab (Herceptin\^®) IV over 30-90 minutes on day 1” NCT00093808

“Trastuzumab (Herceptin®) IV over 30-90 minutes on day 1.” NCT00796978

“who failed one prior trastuzumab (Herceptin®) treatment” NCT01125566

“trastuzumab (Herceptin) IV over 30-90 minutes on day 1.” NCT00003992

“trastuzumab (Herceptin) IV over 30-90 minutes on day 1” NCT00054470

“trastuzumab (Herceptin) IV over 60-90 minutes on day 1” NCT00053339

“Anti-HER-2 Monoclonal Antibody Trastuzumab (Herceptin)” NCT00006228

“trastuzumab (Herceptin®)-naive vs trastuzumab-failure” NCT00086957

“anthracyclines and taxotere with or without HerceptinNCT02679040

“trastuzumab (Herceptin®) IV over 90 minutes on day 1” NCT00084513

“trastuzumab (Herceptin®) IV over 30-90 minutes” NCT00820872

“trastuzumab (Herceptin®) IV over 30-90 minutes” NCT00301899

“trastuzumab (Herceptin \^®) IV over 90 minutes” NCT00088985

“trastuzumab (Herceptin) IV over 30-90 minutes” NCT00019812

“trastuzumab (Herceptin\^®) IV over 90 minutes” NCT00085020

“trastuzumab (Herceptin®) IV over 90 minutes” NCT00103233

“Trastuzumab (Herceptin®) IV once weekly” NCT00674414

“Patients receive trastuzumab (HerceptinNCT00104949

“monoclonal antibody HER2 (Herceptin)” NCT00003539

Herceptin (Trastuzumab fpr Her2 pos)” NCT01426880

“EU-sourced Trastuzumab (Herceptin®)” NCT04670796

“Trastuzumab (also called Herceptin)” NCT01205217

“Drug: trastuzumab (Herceptin®)” NCT00022672

“* Trastuzumab (Herceptin®)” NCT03765983

“trastuzumab (Herceptin®)” NCT00138125

“trastuzumab (Herceptin®)” NCT01104571

“traztuzumab (Herceptin®)” NCT02167854

“trastuzumab (Herceptin®)” NCT00433407

Herceptin (trastuzumab)” NCT04109391

“trastuzumab [Herceptin]” NCT02402712

“Trastuzumab (Herceptin)” NCT07193394

“Trastuzumab (Herceptin)” NCT07565324

“trastuzumab (Herceptin)” NCT00095706

“Trastuzumab [Herceptin]” NCT01130337

“trastuzumab [Herceptin]” NCT00964704

Herceptin (trastuzumab)” NCT00724360

“trastuzumab [Herceptin]” NCT01290718

“trastuzumab [Herceptin]” NCT00717405

“Trastuzumab (Herceptin)” NCT07527806

“trastuzumab (Herceptin)” NCT00251433

“Trastuzumab (Herceptin)” NCT07610720

“trastuzumab [Herceptin]” NCT00811135

“trastuzumab (Herceptin)” NCT00004925

Herceptin (trastuzumab)” NCT01548677

“trastuzumab [Herceptin]” NCT00885755

“trastuzumab [Herceptin]” NCT01260194

“trastuzumab [Herceptin]” NCT01363986

“Trastuzumab (Herceptin)” NCT06876714

“trastuzumab [Herceptin]” NCT00444587

“Drug: HerceptinNCT00493649

NCT01450696

NCT03084237

NCT00337649

NCT00440622

NCT00129896

NCT04905667

NCT00429104

NCT00496808

NCT00800436

NCT03013504

NCT01566721

NCT03013881

NCT00545688

NCT01004172

NCT02380131

NCT00189579

NCT03989037

NCT02015156

NCT01401166

NCT00004067

NCT00041470

NCT03180242

NCT03433313

NCT00133796

NCT01649271

NCT01503905

NCT00372424

NCT02748213

NCT00470704

NCT00127933

NCT03058939

NCT00043394

NCT00021255

NCT01570036

NCT02581748

NCT00004935

NCT00470847

NCT00453635

NCT05301530

NCT05301010

NCT01603264

NCT05629949

NCT00148681

NCT00045032

NCT02581462

NCT00031278

NCT00433095

NCT03238495

NCT03879577

NCT02721641

NCT01084876

NCT01989676

NCT01084863

NCT03161353

NCT05593094

NCT03907800

NCT00148668

NCT00191451

NCT03242239

NCT01097460

NCT00136539

NCT00005926

NCT00038402

Known as Herceptin (trastuzumab) “Herceptin® (trastuzumab)” NCT00365365
1

Herceptin (trastuzumab)NCT00412412

Known as Herceptin EU ClinicalTrials.gov intervention name — accepted as the source's own label NCT02594761
Known as Herceptin Hylecta ClinicalTrials.gov intervention name — accepted as the source's own label NCT07299955
Known as Herceptin US ClinicalTrials.gov intervention name — accepted as the source's own label NCT02594761
Known as Herzuma “D1 Nanoxel 75 mg/m2 + D5W 100mL MIV over 1hr D1 Herzuma 8mg/kg (loading dose) + N/S 250mL miv over 90mins 6mg/kg (maintenance) + N/S 250mL MIV over 30mins (since 2 cycle)...” NCT03614364
4

“Combination of pertuzumab and the trastuzumab biosimilar CT-P6 (Herzuma®) in Her2-positive breast cancer susceptible to neoadjuvant chemotherapy.” NCT06907082

Herzuma (Trastuzumab-pkrb) 4mg/kg after 6mg/kg loading D1” NCT04722133

NCT03755141

NCT04817540

Known as NSC-688097 “Docetaxel (NSC-628503) And Vinorelbine (NSC-608210) Plus Filgrastim (NSC-614629) With Weekly Trastuzumab (NSC-688097) For HER-2 Positive, Stage IV Breast Cancer” NCT00041067
1

“Trastuzumab (Herceptin®) (NSC-688097)” NCT00103233

Known as Ontruzant ClinicalTrials.gov intervention name — accepted as the source's own label NCT05036005
Known as QL1701 QL1701 (Trastuzumab for Injection): First dose 8mg/kg, then 6mg/kg, every 3 weeks, for a total of 6 cycles” NCT07299890
1

NCT05629949

Known as QL1701 (A trastuzumab biosimilar produced by Qilu Pharmaceutical Co., Ltd) QL1701 (A trastuzumab biosimilar produced by Qilu Pharmaceutical Co., Ltd)NCT07187752
Known as RhuMab HER2 “Phase II and Pharmacokinetic Study of CPT-11 and Trastuzumab (RhuMab HER2, Herceptin) in Advanced Colo-Rectal Cancer With p185 HER 2 Overexpression” NCT00003995
Known as SB3 “Thereafter, SB3 6 mg/kg will be infused over 30 minutes on day 1 of each subsequent 21-day cycle until progression or unacceptable toxicity.” NCT05530057
1

NCT02149524

Known as Tmab “Trastuzumab (Tmab), pertuzumab (Pmab), and taxane has been a standard first-line treatment for recurrent or metastatic human epidermal growth factor (HER2)-positive breast...” PMID 32381018 May 2020
Known as Tras Trastuzumab (Tras) was administered as an open-label, commercial product at an initial dose of 8 mg/kilograms (kg) over a 90-minute intravenous infusion, followed by 6 mg/kg...” NCT02393248
Known as trastuzumab (Herceptine) trastuzumab (Herceptine)NCT02059876
Known as Trastuzumab (T) Trastuzumab (T)NCT03262935