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临床试验/NCT04914520
NCT04914520已完成1 期

A Phase 1 Study to Assess the Safety, Tolerability, and Immunogenicity of VN-0200 After Intramuscular Injections in Japanese Healthy Adults and Elderly Subjects

Daiichi Sankyo Co., Ltd.2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2021年6月11日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
48
试验地点
2
主要终点
Number of Participants Reporting Treatment-emergent Adverse Events

研究概览

简要总结

This study will assess the safety, tolerability, and immunogenicity of VN-0200 after intramuscular injections in Japanese healthy adults and elderly subjects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adults aged ≥20 and ≤50 years (Step 1) or healthy elderly aged ≥65 and ≤80 years (at the time of informed consent)
  • Body mass index (BMI) is ≥18.0 and <30.0 kg/m^2 (at screening)

排除标准

  • Participants with a history of anaphylaxis or severe allergies due to food, medicine, insect bites, cosmetics, or vaccination
  • Having alcohol or drug dependence, etc.

结局指标

主要结局

Number of Participants Reporting Treatment-emergent Adverse Events

时间窗: From first administration through 28 days post second administration

Number of Participants Reporting Local and Systemic Adverse Events

时间窗: From first administration up to 14 days after second administration

Number of Participants Reporting Serious Adverse Events

时间窗: From date of informed consent up to approximately 3 months

次要结局

  • Geometric Mean Fold Rise (GMFR) of Anti-RSV Specific Neutralizing Activity(Day 29 and Day 57 post-dose and at the time of discontinuation (whichever occurs first), up to approximately 2 months)
  • Geometric Mean Titer (GMT) of Anti-VAGA-9001a IgG(Day 1 (pre-dose), Day 29 and Day 57 post-dose, and at the time of discontinuation (whichever occurs first), up to approximately 2 months)
  • Geometric Mean Titer (GMT) of Anti-RSV IgG(Day 1 (pre-dose), Day 29 and Day 57 post-dose, and at the time of discontinuation (whichever occurs first), up to approximately 2 months)
  • Number of IFN-γ spot-forming cells in PBMC Detected by ELISPOT(Day 1 (pre-dose), Day 29 and Day 57 post-dose, and at the time of discontinuation (whichever occurs first), up to approximately 2 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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