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Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine

Sanofi Pasteur, a Sanofi Company · FDA-approved active Biologic Quality 5/100

Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine is a Biologic drug developed by Sanofi Pasteur, a Sanofi Company. It is currently FDA-approved. Also known as: TRIMOVAX™, AVAXIM™.

At a glance

Generic nameAttenuated Measles Mumps Rubella; Inactivated Hep A vaccine
Also known asTRIMOVAX™, AVAXIM™
SponsorSanofi Pasteur, a Sanofi Company
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

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Frequently asked questions about Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine

What is Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine?

Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine is a Biologic drug developed by Sanofi Pasteur, a Sanofi Company.

Who makes Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine?

Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine is developed and marketed by Sanofi Pasteur, a Sanofi Company (see full Sanofi Pasteur, a Sanofi Company pipeline at /company/sanofi).

Is Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine also known as anything else?

Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine is also known as TRIMOVAX™, AVAXIM™.

What development phase is Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine in?

Attenuated Measles Mumps Rubella; Inactivated Hep A vaccine is FDA-approved (marketed).

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