Last reviewed · How we verify

H1N1 vaccination

University of Pennsylvania · FDA-approved active Biologic Quality 5/100

The H1N1 vaccination developed by the University of Pennsylvania is currently marketed, positioning it as an established player in the influenza vaccine market. A key strength is the protection of its core composition through a patent expiring in 2028, providing a significant period of exclusivity. The primary risk lies in the competitive landscape, where multiple other H1N1 vaccines are also available, potentially impacting market share.

At a glance

Generic nameH1N1 vaccination
SponsorUniversity of Pennsylvania
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

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: