JPRN-jRCT2080223428已完成1 期
A Phase 1 Study of the Safety, Tolerability, and Efficacy of Anti-LAG-3 Monoclonal Antibody (BMS-986016) Administered Alone and in Combination with Anti-PD-1 Monoclonal Antibody (Nivolumab, BMS-936558) in Advanced Solid Tumors
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 27
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
- 年龄范围
- >= 20age old 至 ot applicable(—)
- 性别
- All
入选标准
- •Must have histologic or cytologic confirmation of an incurable solid malignancy that is advanced (metastatic and/or unresectable)
- •Must have received, and then progressed or been intolerant to, standard treatment regimen in the advanced or metastatic setting, if such a therapy exists
- •Presence of at least one lesion with measurable disease as defined by RECIST v1.1 criteria for response assessment
排除标准
- •Known or suspected CNS (central nervous system) metastases or with the CNS as the only site of active disease
- •Other concomitant malignancies (with some exceptions per protocol)
- •Any active autoimmune disease or history of known or suspected autoimmune disease
- •History of uncontrolled or significant cardiovascular disease
研究者
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