EUCTR2015-004914-79-ES进行中(未招募)1 期
A Phase 1/2a Study of BMS-986205 Administered in Combination With Nivolumab (BMS-936558, Anti-PD-1 Monoclonal Antibody) in Advanced Malignant Tumors
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 288
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients must have been diagnosed with cancer and had at least 1 prior standard treatment
- •Must be able to swallow pills or capsules
- •Eastern Cooperative Oncology Group(ECOG) Performance Status 0-1
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 173
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 115
排除标准
- •Any prior ongoing clinical study with Nivolumab with overall survival as an endpoint
- •Requirement for daily supplemental oxygen
- •Myocardial infarction or stroke/transient ischemic attack within the past 6 months
- •Uncontrolled angina within the past 3 months
- •History of any chronic Hepatitis, active Hepatitis B or C, human immunodeficiency virus(HIV), or acquired immune deficiency syndrome(AIDS)
研究者
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