JPRN-jRCT2071220068招募中1 期
A Single Ascending Dose Study of DSP-0378 in Healthy Japanese Adult Male Subjects
Ishikawa Tatsuya0 个研究点目标入组 88 人开始时间: 2022年11月7日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 88
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 <= 50age old(—)
- 性别
- Male
入选标准
- •1. Healthy Japanese adult male subject between 20 and 50 years of age (inclusive) at time of informed consent.
- •2. Subject's body weight is between 50.0 kg and 80.0 kg, and body mass index (BMI) is at least 18 kg/m2 but no more than 25 kg/m2.
排除标准
- •1. Subject with a history of clinically significant cardiovascular, hepatic, renal, endocrine, gastrointestinal, hematological, respiratory, psychiatric, neurologic disease, and who considered ineligible for the study by the Principal Investigator or Sub-Investigator.
- •2. Subject who has a presence or history of any medically diagnosed psychiatric disorder (including
- •intellectual disability and substance-related disorders).
- •3. Subject who answers ''yes'' to ''Suicidal Ideation'' Items 4 or 5 on the Columbia-Suicide Severity
- •Rating Scale (C-SSRS) at clinic admission.
- •4. Subject with a history of substance abuse, drug abuse, or a positive urine drug screening at screening
- •visit or clinic admission.
- •5. Subject who has clinical symptoms suggestive of infection with a positive severe acute respiratory
- •syndrome coronavirus 2 (SARS-CoV-2), or has a positive SARS-CoV-2 nucleic acid amplification
- •test at clinic admission.
- •6. Subject who has received a vaccine within 7 days prior to screening visit or clinic admission.
- •7. Subject who is in the opinion of the Principal Investigator or Sub-Investigator, unsuitable in any other
- •way to participate in this study.
研究者
相似试验
进行中(未招募)
1 期
A Single and Multiple Dose Study of DSP-9632PJPRN-jRCT2071210088akamura Hiroki80
已完成
1 期
A phase 1 Multiple Ascending Dose Study of DS-3201b in Subjects with LymphomasRelapsed non-hodgkin lymphomaJPRN-jRCT2080223118DAIICHI SANKYO CO., LTD.100
已完成
不适用
PC-SOD NE (Phase I) -Repeated Dose Study in healthy volunteersidiopathic pulmonary fibrosisJPRN-UMIN000008921TT Bio Pharma Co., LTD.8
进行中(未招募)
不适用
Single-Dose, Dose Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics and Bronchodilatory Effects of Glycopyrrolate Inhalation Solution (GIS) Using a High Efficiency Nebulizer in Patients with COPDChronic Obstructive Pulmonary Disease (COPD)MedDRA version: 9.1Level: LLTClassification code 10010952Term: COPDEUCTR2009-010821-38-GBElevation Pharmaceuticals, Inc12
已完成
不适用
A phase 1 single ascending dose study in healthy subjects to evaluate safety, tolerability, and pharmacokinetics of XVR011COVID-1910047438NL-OMON49939ExeVir Bio BV30
