JPRN-UMIN000047230尚未招募未知
Treatment effect and prediction survival of Immune checkpoint inhibitors by FDG-PET: A multicenter prospective study - Treatment effect and prediction survival of Immune checkpoint inhibitors by PET: A multicenter prospective study
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 100
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
- 20years-old 至 100years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •- That cannot keep a posture of facing upward because of pains in succession for around 30 minutes - During the pregnancy or pregnancy with the possibility - The extreme claustrophobia - The one where progress after treatment being refused, and curing became unidentified - In addition, the person who judges that a manager for study is inappropriate
研究者
相似试验
招募中
Unknown
Study on host immune response during treatment of patients with pulmonary nontuberculous mycobacterial diseasepulmonary nontuberculous mycobacterial diseaseJPRN-UMIN000049658Department of Respiratory Medicine, University of Tsukuba100
进行中（未招募）
1 期
The ability to induce an immune response, efficacy and safety of treatment with Human-cl rhFVIII in previously Untreated Patients, affected by inherited gender-related coagulation disorder ,in which affected males do not produce functional coagulation factor VIII (FVIII) in sufficient quantities to achieve satisfactory blood clotting.Severe Haemophilia AMedDRA version: 20.0Level: LLTClassification code 10018938Term: Haemophilia A (Factor VIII)System Organ Class: 100000004850EUCTR2012-002554-23-ITOCTAPHARMA AG108
进行中（未招募）
1 期
The ability to induce an immune response, efficacy and safety of treatment with Human-cl rhFVIII in previously Untreated Patients ,affected by inherited gender-related coagulation disorder ,in which affected males do not produce functional coagulation factor VIII (FVIII) in sufficient quantities to achieve satisfactory blood clotting.Severe Haemophilia AMedDRA version: 20.0Level: LLTClassification code 10018938Term: Haemophilia A (Factor VIII)System Organ Class: 100000004850EUCTR2012-002554-23-PLOCTAPHARMA AG108
进行中（未招募）
1 期
The ability to induce an immune response, efficacy and safety of treatment with Human-cl rhFVIII in previously Untreated Patients ,affected by inherited gender-related coagulation disorder ,in which affected males do not produce functional coagulation factor VIII (FVIII) in sufficient quantities to achieve satisfactory blood clotting.Severe Haemophilia AMedDRA version: 15.1Level: LLTClassification code 10018938Term: Haemophilia A (Factor VIII)System Organ Class: 100000004850EUCTR2012-002554-23-ESOCTAPHARMA AG100
进行中（未招募）
1 期
The ability to induce an immune response, efficacy and safety of treatment with Human-cl rhFVIII in previously Untreated Patients ,affected by inherited gender-related coagulation disorder ,in which affected males do not produce functional coagulation factor VIII (FVIII) in sufficient quantities to achieve satisfactory blood clotting.Severe Haemophilia AMedDRA version: 18.0Level: LLTClassification code 10018938Term: Haemophilia A (Factor VIII)System Organ Class: 100000004850EUCTR2012-002554-23-HROCTAPHARMA AG108