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Seasonal trivalent influenza vaccine, Anflu®

Center for Disease Prevention and Control of Beijing Military Region · FDA-approved active Biologic

The vaccine stimulates the immune system to produce antibodies and cellular immunity against three seasonal influenza virus strains.

The vaccine stimulates the immune system to produce antibodies and cellular immunity against three seasonal influenza virus strains. Used for Prevention of seasonal influenza caused by influenza A and B viruses.

At a glance

Generic nameSeasonal trivalent influenza vaccine, Anflu®
Also known asAnflu®
SponsorCenter for Disease Prevention and Control of Beijing Military Region
Drug classinactivated influenza vaccine
ModalityBiologic
Therapeutic areaImmunology
PhaseFDA-approved

Mechanism of action

Seasonal trivalent influenza vaccines contain inactivated or attenuated viral antigens from three circulating influenza strains (typically two A subtypes and one B type). Upon administration, the vaccine triggers both humoral (antibody) and cell-mediated immune responses, enabling the body to recognize and neutralize these specific influenza viruses if encountered naturally, thereby preventing infection or reducing disease severity.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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