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Clinical Trial Summary

To evaluate the non inferiority of the immunogenicity of the test vaccine inoculated according to the four dose immunization program over the five dose immunization program and the batches consistency of immunogenicity according to five dose immunization procedures.


Clinical Trial Description

- In the population aged 10-60 years, evaluate the non inferiority of the immunogenicity of the test vaccine inoculated according to the four dose immunization program (0, 3, 7, 14/28 days) over the five dose immunization program (0, 3, 7, 14, 28 days); - To evaluate the consistency of immunogenicity between batches of freeze-dried human rabies vaccine (Vero cell) inoculated according to five dose immunization procedures (0, 3, 7, 14, 28 days). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05545371
Study type Interventional
Source Changchun Zhuoyi Biological Co., Ltd
Contact
Status Enrolling by invitation
Phase Phase 3
Start date June 18, 2022
Completion date December 30, 2024

See also
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Completed NCT04495569 - A Bridging Study of the SYN023 on Healthy Adult Subjects Phase 1/Phase 2
Recruiting NCT05382650 - Survey of Human Rabies Immune Globulin Safety in Children
Completed NCT04213950 - Improving Adherence to Rabies PEP Guideline Recommendations N/A