CTRI/2018/11/016306Other未知
Multicenter, Observational Registry to Study the Safety and Efficacy of Biosimilar Trastuzumab Intravenous Infusion in Patients with Early Breast Cancer
试验速览
- 阶段
- 未知
- 状态
- Other
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Patient aged ââ?°Â¥ 18 years
- •Patients who are willing to provide written and signed informed consent for collecting health data into the registry
- •Patients with EBC who are eligible to receive treatment with Trastuzumab as per the approved prescribing information and clinical judgment of the treating oncologist
排除标准
- •1.Have a history of hypersensitivity to Trastuzumab or other components of the product
- •2.Patient with any contraindication as mentioned in approved prescribing information of Trastuzumab biosimilar
- •3.Any other reason (concurrent disease or condition) in the opinion of the oncologist that would make the patient unsuitable for participation in the registry
研究者
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