The Phase 1 clinical trial of the freeze-dried human rabies vaccine (human diploid cells) will be conducted on participants aged 10 to 60. This study will design a single-arm, randomized, open-access trial with different immunization schedules (5-dose schedule and 2-1-1 schedule) to evaluate the safety and tolerability of the vaccine in participants aged 10 to 60
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The occurrence of AE and AR within 30 minutes after each dose of vaccination
Timeframe: within 30 minutes after each dose of vaccination
The occurrence of AE and AR within 7 days after each dose of vaccination
Timeframe: within 7 days after each dose of vaccination
The occurrence of AE and AR within 30 days from the first dose of vaccination to the full course of vaccination
Timeframe: within 30 days from the first dose of vaccination to the full course of vaccination
Abnormal changes /Occurrence of clinically significant abnormal changes in laboratory test indicators
Timeframe: the third day after the first dose of vaccination
The occurrence of serious adverse events
Timeframe: within 6 months from the first dose of vaccination to the full course of vaccination.