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Intravitreal Aflibercept Injection 2mg

Tennessee Retina · FDA-approved active Small molecule Quality 2/100

Intravitreal Aflibercept Injection 2mg, marketed by Tennessee Retina, holds a significant position in the ophthalmic therapeutic market. The key composition patent, set to expire in 2028, provides a strong competitive advantage by protecting the drug's unique formulation. The primary risk is the potential increase in competition post-patent expiry, which could impact market share and revenue.

At a glance

Generic nameIntravitreal Aflibercept Injection 2mg
Also known asAflibercept; EYLEA®; VEGF Trap-Eye, IAI; EYLEA®; BAY86-5321; VEGF Trap-Eye
SponsorTennessee Retina
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

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

Competitive intelligence

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