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IlUVIEN

Association for Innovation and Biomedical Research on Light and Image · FDA-approved active Small molecule Quality 2/100

IlUVIEN, marketed by the Association for Innovation and Biomedical Research on Light and Image, holds a niche position in the ophthalmic market with its unique mechanism of action. The drug's key strength lies in its key composition patent, which is set to expire in 2028, providing a period of exclusivity and potential revenue protection. The primary risk to IlUVIEN is the lack of clear primary indication and revenue data, which may limit its market penetration and investor confidence.

At a glance

Generic nameIlUVIEN
Also known asFluocinolone Acetonide, Fluocinolone Acetonide Intravitreal Implant 0.19 mg
SponsorAssociation for Innovation and Biomedical Research on Light and Image
ModalitySmall molecule
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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