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Trivalent inactivated influenza vaccine

Sanofi · FDA-approved active Biologic Quality 2/100

Trivalent inactivated influenza vaccine is a Biologic drug developed by Sanofi. It is currently FDA-approved. Also known as: Fluzone®, Vaxigrip, Brand Name: VAXIGRIP, Vaxigrip Junior.

Sanofi's Trivalent inactivated influenza vaccine is a marketed product with a well-established presence in the influenza vaccine market. The key composition patent is set to expire in 2028, providing a period of exclusivity that supports current market positioning. The primary risk is the potential increase in competition following the patent expiry, which could impact revenue and market share.

At a glance

Generic nameTrivalent inactivated influenza vaccine
Also known asFluzone®, Vaxigrip, Brand Name: VAXIGRIP, Vaxigrip Junior, Fluzone
SponsorSanofi
ModalityBiologic
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

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Frequently asked questions about Trivalent inactivated influenza vaccine

What is Trivalent inactivated influenza vaccine?

Trivalent inactivated influenza vaccine is a Biologic drug developed by Sanofi.

Who makes Trivalent inactivated influenza vaccine?

Trivalent inactivated influenza vaccine is developed and marketed by Sanofi (see full Sanofi pipeline at /company/sanofi).

Is Trivalent inactivated influenza vaccine also known as anything else?

Trivalent inactivated influenza vaccine is also known as Fluzone®, Vaxigrip, Brand Name: VAXIGRIP, Vaxigrip Junior, Fluzone.

What development phase is Trivalent inactivated influenza vaccine in?

Trivalent inactivated influenza vaccine is FDA-approved (marketed).

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