
Ogivri440 mg/20
Beximco Pharmaceuticals Ltd.
Trastuzumab is a HER2-targeted monoclonal antibody indicated for the treatment of certain HER2-overexpressing cancers, confirmed by an approved HER2 test prior to initiation.
Trastuzumab is a HER2-targeted monoclonal antibody indicated for the treatment of certain HER2-overexpressing cancers, confirmed by an approved HER2 test prior to initiation.
Trastuzumab must only be used in patients whose tumors have confirmed HER2 overexpression or gene amplification, as efficacy depends entirely on HER2-positive status.
Trastuzumab dosing is indication-specific and must be individualized by the treating oncologist. It is given as an intravenous infusion only — never as an intravenous push or bolus.
| Indication | Loading dose | Maintenance dose | Duration |
|---|---|---|---|
| Adjuvant breast cancer (Regimen A) | 4 mg/kg IV over 90 minutes | 2 mg/kg IV weekly over 30 minutes (with paclitaxel/docetaxel), then 6 mg/kg every 3 weeks | Total of 52 weeks |
| Adjuvant breast cancer (Regimen B) | 8 mg/kg IV over 90 minutes | 6 mg/kg IV every 3 weeks over 30–90 minutes | Total of 52 weeks |
| Metastatic breast cancer | 4 mg/kg IV over 90 minutes | 2 mg/kg IV weekly over 30 minutes | Until disease progression or unacceptable toxicity |
| Metastatic gastric/GEJ adenocarcinoma | 8 mg/kg IV over 90 minutes | 6 mg/kg IV every 3 weeks over 30–90 minutes | Until disease progression or unacceptable toxicity |
If a scheduled dose is missed or delayed, the treating physician determines whether a reloading dose is required based on the interval since the last dose. See Administration for infusion technique and monitoring, and Reconstitution for preparation of the intravenous powder for injection.
Serious adverse effects of Trastuzumab — cardiomyopathy, infusion reactions, pulmonary toxicity, and embryo-fetal toxicity — are described fully in Precautions and Warnings and are not repeated here.
Patients should promptly report shortness of breath, swelling of the legs, palpitations, unusual bruising or bleeding, or persistent fever to their treating physician.
Trastuzumab is contraindicated in patients with:
Trastuzumab should not be initiated in patients who are pregnant or planning pregnancy because of confirmed risk of fetal harm (see Pregnancy and Lactation); this is a strict avoidance rather than a formal labeled contraindication in all regulatory labels, so the treating physician must weigh this carefully before use.
Disclaimer
The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.