drugset / Trial / NCT04188691
A Clinical Trial to Evaluate the Safety and Immunogenicity of Norovirus Bivalent Vaccine
Phase 1
Completed
510 enrolled
National Vaccine and Serum Institute, China
Beijing Zhong Sheng Heng Yi Pharmaceutical Technology Co., Ltd. · collabLanzhou Institute of Biological Products Co., Ltd · collabZhengzhou University · collab
RandomizedParallel-groupDouble-blindPrevention
Summary
A total of 450 subjects were enrolled, divided into four age groups, including 18-59 years, 6-17 years, 3-5 years, and 6-35 months. There are three types of the test vaccine component in each age group. A total of 30 people in each dose group were vaccinated with the test vaccine or placebo 1 or placebo 2, respectively, in a ratio of 3: 1: 1. The 18-59-year-old, 6-17-year-old, and 3-5-year-old age groups were vaccinated 2 times at a time interval of 28 days. The 6-35 month age group is divided into two groups, Group 1 is inoculated with 2 doses interval of 28 days each, and Group 2 is inoculated with 3 doses interval of 28 days.
Timeline
- Start
- 2019-11-28
- Primary completion
- 2020-12-13
- Completion
- 2020-12-13
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Norovirus Bivalent (GI.1 / GII.4) Vaccine | Vaccine | 0.5 ml | Intramuscular |