Last reviewed · How we verify
Nepafenac 0.3%
At a glance
| Generic name | Nepafenac 0.3% |
|---|---|
| Also known as | Ilevro |
| Sponsor | Intuor Technologies, Inc. |
| Modality | Small molecule |
| Phase | Phase 1 |
Approved indications
Common side effects
- Intraocular pressure increased
- Headache
- Blood glucose increased
- Anterior chamber inflammation
- Eye pain
- Posterior capsule opacification
- Urinary tract infection
- Conjunctival cyst
- Corneal oedema
- Macular oedema
- Vitreous detachment
- Vomiting
Key clinical trials
- The TRIBECA Study (TRIessence/Byqlovi for Easier CAtaract Surgery) (PHASE4)
- Comparing Efficacy of Bromfenac 0.09%, Nepafenac 0.3% and Diclofenac 0.1% in Patients After Cataract Surgery (NA)
- Clinical Endpoint Study of Nepafenac 0.3% Opthalmic Suspension (PHASE3)
- Post Intravitreal Injection Topical NSAID vs. Patching (PHASE4)
- Study Title: Clinical Outcomes of Prolensa (Bromfenac Ophthalmic Solution) 0.07% QD vs. Ilevro (Nepafenac Ophthalmic Suspension) 0.3% QD With Extra (Pulse) Dose on Day of Surgery for Treatment of Ocular Inflammation Associated With Cataract Surgery in a Randomized, Single Masked Clinical Trial (PHASE4)
- Prospective Study With Adjunctive Once Daily Topical Nepafenac 0.3% Versus Placebo (NA)
- Prolensa (Bromfenac) 0.07% QD vs. Ilevro (Nepafenac) 0.3% QD for Treatment of Ocular Inflammation Post Cataract Surgery (NA)
- PGE2 Levels in Patient Treated With NSAIDs (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial 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:
- Nepafenac 0.3% CI brief — competitive landscape report
- Nepafenac 0.3% updates RSS · CI watch RSS
- Intuor Technologies, Inc. portfolio CI