CTRI/2016/01/006493进行中(未招募)3 期
A Phase 3, Randomised, Parallel-Group, Active-Controlled, Double Blind Study to Compare Efficacy and Safety between CT P10 and Rituxan in Patients with Low Tumour Burden Follicular Lymphoma - CT-P10 3.4
试验速览
- 阶段
- 3 期
- 状态
- 进行中(未招募)
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Key brief inclusion criteria:
- •Confirmed diagnosis of low tumour burden, CD20+ follicular lymphoma grade 1 to 3a according to the World Health Organization 2008 classification
- •Ann Arbor Stage II, III or IV
排除标准
- •Key brief exclusion criteria:
- •Has received rituximab
- •Allergies or hypersensitivity to murine, chimeric, human or humanised proteins
- •Previous treatment for NHL
- •Any malignancy, patient has known central nervous system involvement or any evidence of spinal cord compression by lymphoma
- •Current or recent treatment with any other investigational medicinal product or device
- •pregnant or lactating
研究者
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招募中
不适用
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