Last reviewed · How we verify
imported compared vaccine
This is an imported vaccine product that stimulates the immune system to prevent infectious disease through antigen presentation and adaptive immune response activation.
This is an imported vaccine product that stimulates the immune system to prevent infectious disease through antigen presentation and adaptive immune response activation. Used for Prevention of infectious disease (specific indication unknown without product specification).
At a glance
| Generic name | imported compared vaccine |
|---|---|
| Sponsor | Beijing Center for Disease Control and Prevention |
| Drug class | vaccine |
| Modality | Biologic |
| Therapeutic area | Immunology |
| Phase | FDA-approved |
Mechanism of action
As a vaccine, it contains antigens (either live attenuated, inactivated, or recombinant) that train the immune system to recognize and respond to specific pathogens. The exact mechanism depends on the vaccine type and target pathogen, but generally involves activation of both humoral (antibody) and cellular (T-cell) immunity to confer protective immunity against infection.
Approved indications
- Prevention of infectious disease (specific indication unknown without product specification)
Common side effects
- Injection site reaction (pain, redness, swelling)
- Fever
- Myalgia
- Fatigue
Key clinical trials
- A Study of SII Yellow Fever Vaccine to Compare Safety and Immunogenicity With STAMARIL (PHASE3)
- Efficacy, Safety and Immunogenicity Evaluation of MTBVAC in Newborns in Sub-Saharan Africa (PHASE3)
- Safety and Immunogenicity of the Butantan Institute Influenza Vaccine Compared to Sanofi Pasteur Influenza Vaccine (PHASE4)
- A Study of SII Yellow Fever Vaccine to Compare Safety and Immunogenicity With STAMARIL® In Healthy Infants (PHASE3)
- Protectivity and Safety Following Recombinant Hepatitis B Vaccine (PHASE2, PHASE3)
- Safety and Immunogenicity Study of Split Influenza Virus Vaccine in Different Age Groups (PHASE4)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |