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These highlights do not include all the information needed to use OGIVRI safely and effectively. See full prescribing information for OGIVRI. OGIVRI® (trastuzumab-dkst) for injection, for intravenous use Initial U.S. Approval: 2017 OGIVRI® (trastuzumab-dkst) is biosimilar* to HERCEPTIN (trastuzumab).
Medication labelWhy this: Advisory · dailymed-prescription
Ogivri is indicated for adjuvant treatment of HER2 overexpressing node positive or node negative (ER/PR negative or with one high risk feature [see Clinical Studies (14.1)]) breast cancer •as part of a treatment regimen consisting of doxorubicin, cyclophosphamide, and either paclitaxel or docetaxel •as part of a treatment regimen with docetaxel and carboplatin •as a single agent following multi-modality anthracycline based therapy. Select patients for therapy based on an FDA-approved companion diagnostic for a trastuzumab product [see Dosage and Administration (2.1)]. Ogivri is indicated: •In combination with paclitaxel for first-line treatment of HER2-overexpressing metastatic breast cancer •As a single agent for treatment of HER2-overexpressing breast cancer in patients who have received one or more chemotherapy regimens for metastatic disease. Select patients for therapy based on an FDA-approved companion diagnostic for a trastuzumab product [see Dosage and Administration (2.1)]. Ogivri is indicated, in combination with cisplatin and capecitabine or 5-fluorouracil, for the treatment of patients with HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma who have not received prior treatment for metastatic disease. Select patients for therapy based on an FDA-approved companion diagnostic for a trastuzumab product [see Dosage and Administration (2.1)].
- generic_name
- trastuzumab-dkst
- brand_name
- trastuzumab, BACTERIOSTATIC WATER
- product_names
- trastuzumab-dkst, trastuzumab, BACTERIOSTATIC WATER
- ndc
- 67457-847, 67457-847-44, 67457-845, 67457-845-50, 67457-846, 67457-846-20, 67457-991, 67457-991-15
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en