Clinical Trial of Freeze-dried Human Rabies Vaccine (Without Serum Vero Cells)

Exclusion Criteria

• •1. A history of rabies vaccine immunization or rabies virus passive immunization was asked;
• •2. A history of grade 2 or 3 injury in animals susceptible to rabies virus (cats, dogs, etc.) within 12 months prior to the first dose of vaccination (the assessment criteria was the Technical Guidelines for Rabies Prevention and Control (2016));
• •3. Plan to participate in other clinical trials during the clinical study;
• •4. Allergic to any component of the test vaccine; History of severe allergies that require medical intervention, such as anaphylactic shock, allergic laryngeal edema, anaphylactoid purpura, thrombocytopenic purpura, allergic necrosis reaction (Arthus reaction), severe urticaria, dyspnea, angioneurotic edema, etc.;
• •5. Have been diagnosed with a congenital or acquired immunodeficiency disease, such as HIV infection, lymphoma, leukemia, systemic lupus erythematosus, rheumatoid arthritis, juvenile rheumatoid arthritis, inflammatory bowel disease, or other immune disease that the investigator has determined may affect the evaluation of the trial;
• •6. Known or suspected serious medical conditions upon inquiry include: severe respiratory diseases, poorly controlled chronic diseases, severe liver and kidney diseases, severe cardiovascular diseases, malignant tumors, etc.;
• •7. \* Medically unmanageable hypertension, such as systolic blood pressure \>120mmHg and/or diastolic blood pressure \>80mmHg in subjects 10 to 17 years of age prior to enrollment, systolic blood pressure of 140mmHg and/or diastolic blood pressure of 90mmHg in subjects 18 years of age and older;
• •8. Coagulation dysfunction (e.g. coagulation factor deficiency, coagulation disorders, platelet abnormalities) or coagulation disorders diagnosed by a physician;
• •9. Asplenia, functional asplenia, and any condition resulting in asplenia or splenectomy;
• •10. Have received immunosuppressive therapy within 3 months prior to vaccination or plan to receive immunosuppressive therapy throughout the study period;
• •11. Plan to receive such treatment within 30 days after the first dose to the full dose, such as long-term systemic glucocorticoid therapy (2 weeks or more at a dose of \>2mg/kg/ day or \>20mg/ day of prednisone or equivalent); Allow topical use (such as ointment, eye drops, inhalants or nasal sprays);
• •12. \* Received immunoglobulins or blood-related products within 3 months prior to vaccination or plan to receive them throughout the study period;
• •13. \* Acute illness or acute onset of chronic disease within 3 days prior to vaccination;
• •14. \* Antipyretic, analgesic and anti-allergic drugs were used within 3 days prior to vaccination;
• •15. \* Have received COVID-19 vaccine or live attenuated vaccine within 28 days prior to vaccination, and have received inactivated vaccines other than COVID-19 inactivated vaccines within 14 days prior to vaccination;
• •16. Previous or current diagnosis of neurological or psychiatric disorders (including but not limited to dementia, schizophrenia, bipolar disorder, etc.) or confirmed Seizures, convulsions (excluding febrile convulsions in children 5 years of age and younger)), and other neuropsychiatric disorders deemed unsuitable for participation in this study by the investigator;
• •17. Due to various medical, psychological, social, or other conditions that, in the judgment of the investigator, are inconsistent with the study protocol or cannot be complied with.
• •For the criteria marked with an (\*), if the subject has the conditions specified in that criteria, the visit may be rescheduled when those conditions are no longer present.
• •In addition to the examination items set by the protocol, other medical history, surgical history, and medication history were obtained in the form of consultation.
• •Criteria for subsequent dose delays:If any of the following conditions occur before any subsequent dose of the subject, the vaccination should be postponed until the vaccination requirements are met.
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• •1. On the day of vaccination, the axillary temperature is measured at 37.3℃ for subjects \>14 years old and 37.5℃ for subjects \<14 years old.
• •2. Acute illness or acute onset of chronic disease within 3 days prior to vaccination;
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• •3. Vaccination-related adverse events occur after vaccination and subsequent doses are not considered appropriate by investigators;
• •4. The investigator determines any circumstances that require discontinuation of vaccination from a subject risk and benefit perspective.
• •1. Incomplete full immunization;
• •2. Vaccination with rabies immunoglobulin or other rabies vaccines within 12 months after full immunization;
• •3. Long-term use (\>15 days) of immunosuppressants or other immunomodulatory drugs (such as glucocorticoids) within 12 months after full vaccination;
• •4. Any other circumstances that the investigator believes may affect the evaluation of the trial.