Created at Source Raw Value Validated value
June 25, 2024, noon usa

* having a history of covid-19 or a positive nucleic acid test for covid-19; * having a history or a family history of allergy, convulsion, epilepsy, brain disease, or mental illness; * being allergic to any component of vaccines, or having a history of severe allergic reaction to any vaccine; * having immunodeficiency disorder, during treatment of malignant tumor, having immunodeficiency induced by immunosuppressants (oral steroid hormones) or hiv, or having a family member with close contact who suffers from congenital immune disorder; * having injection of non-specific immunoglobulin within 1 month prior to enrollment; * having acute febrile illness or communicable disease; * having a history of confirmed thrombocytopenia or other coagulation disorders, which may cause contraindications for a subcutaneous injection; * having severe chronic disease or acute exacerbation of chronic disease, or having uncontrolled hypertension or diabetes; * having various infectious, pyogenic, or allergic skin diseases; * women in pregnancy or lactation or participants who plan for a baby within 3 months after vaccination should delay the vaccination; * having any condition that may affect trial assessment as determined by researchers. exclusion criteria for the second dose: * having any serious adverse event related to the first dose vaccination; * after vaccination, having systemic adverse reaction or allergic reaction with a severity of grade 3 or higher as determined by researchers; * having a newly emerging condition that meets the exclusion criteria for the first dose; * having any condition that may affect trial assessment as determined by researchers.

* having a history of covid-19 or a positive nucleic acid test for covid-19; * having a history or a family history of allergy, convulsion, epilepsy, brain disease, or mental illness; * being allergic to any component of vaccines, or having a history of severe allergic reaction to any vaccine; * having immunodeficiency disorder, during treatment of malignant tumor, having immunodeficiency induced by immunosuppressants (oral steroid hormones) or hiv, or having a family member with close contact who suffers from congenital immune disorder; * having injection of non-specific immunoglobulin within 1 month prior to enrollment; * having acute febrile illness or communicable disease; * having a history of confirmed thrombocytopenia or other coagulation disorders, which may cause contraindications for a subcutaneous injection; * having severe chronic disease or acute exacerbation of chronic disease, or having uncontrolled hypertension or diabetes; * having various infectious, pyogenic, or allergic skin diseases; * women in pregnancy or lactation or participants who plan for a baby within 3 months after vaccination should delay the vaccination; * having any condition that may affect trial assessment as determined by researchers. exclusion criteria for the second dose: * having any serious adverse event related to the first dose vaccination; * after vaccination, having systemic adverse reaction or allergic reaction with a severity of grade 3 or higher as determined by researchers; * having a newly emerging condition that meets the exclusion criteria for the first dose; * having any condition that may affect trial assessment as determined by researchers.

Oct. 16, 2021, 3 p.m. usa

- having a history of covid-19 or a positive nucleic acid test for covid-19; - having a history or a family history of allergy, convulsion, epilepsy, brain disease, or mental illness; - being allergic to any component of vaccines, or having a history of severe allergic reaction to any vaccine; - having immunodeficiency disorder, during treatment of malignant tumor, having immunodeficiency induced by immunosuppressants (oral steroid hormones) or hiv, or having a family member with close contact who suffers from congenital immune disorder; - having injection of non-specific immunoglobulin within 1 month prior to enrollment; - having acute febrile illness or communicable disease; - having a history of confirmed thrombocytopenia or other coagulation disorders, which may cause contraindications for a subcutaneous injection; - having severe chronic disease or acute exacerbation of chronic disease, or having uncontrolled hypertension or diabetes; - having various infectious, pyogenic, or allergic skin diseases; - women in pregnancy or lactation or participants who plan for a baby within 3 months after vaccination should delay the vaccination; - having any condition that may affect trial assessment as determined by researchers. exclusion criteria for the second dose: - having any serious adverse event related to the first dose vaccination; - after vaccination, having systemic adverse reaction or allergic reaction with a severity of grade 3 or higher as determined by researchers; - having a newly emerging condition that meets the exclusion criteria for the first dose; - having any condition that may affect trial assessment as determined by researchers.

- having a history of covid-19 or a positive nucleic acid test for covid-19; - having a history or a family history of allergy, convulsion, epilepsy, brain disease, or mental illness; - being allergic to any component of vaccines, or having a history of severe allergic reaction to any vaccine; - having immunodeficiency disorder, during treatment of malignant tumor, having immunodeficiency induced by immunosuppressants (oral steroid hormones) or hiv, or having a family member with close contact who suffers from congenital immune disorder; - having injection of non-specific immunoglobulin within 1 month prior to enrollment; - having acute febrile illness or communicable disease; - having a history of confirmed thrombocytopenia or other coagulation disorders, which may cause contraindications for a subcutaneous injection; - having severe chronic disease or acute exacerbation of chronic disease, or having uncontrolled hypertension or diabetes; - having various infectious, pyogenic, or allergic skin diseases; - women in pregnancy or lactation or participants who plan for a baby within 3 months after vaccination should delay the vaccination; - having any condition that may affect trial assessment as determined by researchers. exclusion criteria for the second dose: - having any serious adverse event related to the first dose vaccination; - after vaccination, having systemic adverse reaction or allergic reaction with a severity of grade 3 or higher as determined by researchers; - having a newly emerging condition that meets the exclusion criteria for the first dose; - having any condition that may affect trial assessment as determined by researchers.