ILEVRO
Peaknepafenac
NDAOPHTHALMICSUSPENSION/DROPS
Approved
Oct 2012
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
16
Data completeness
6/8 — Strong
ILEVRO (nepafenac) is cyclooxygenase inhibitors [moa]. First approved in 2012.
Drug data last refreshed 2d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ILEVRO is a topical ophthalmic suspension containing nepafenac, a nonsteroidal anti-inflammatory drug (NSAID) that works by inhibiting cyclooxygenase enzymes. It was approved by the FDA on October 16, 2012, and is indicated for reduction of pain and inflammation associated with cataract surgery and other ocular conditions. The drug is administered as eye drops and represents a key anti-inflammatory option in the ophthalmology treatment landscape for perioperative pain management.
$0.0BPart D
5.9 years to LOEMechanism of Action
Cyclooxygenase Inhibitors
Pharmacologic Class:
Nonsteroidal Anti-inflammatory Drug
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (16)
Tolerability and Toxicity of Topically Applied Nepafenac 0.3% vs Ketorolac 0.5%
Started Apr 2016
200 enrolled
Cataract
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
Started Oct 2013
57 enrolled
Treatment of Ocular Inflammation Associated With Cataract Surgery
Nepafenac Once Daily for Macular Edema - Study 2
Started Jun 2013
819 enrolled
Non-Proliferative Diabetic RetinopathyCataract
Nepafenac Once Daily for Macular Edema - Study 1
Started Jun 2013
881 enrolled
Non-Proliferative Diabetic RetinopathyCataract
Prolensa (Bromfenac) 0.07% QD vs. Ilevro (Nepafenac) 0.3% QD for Treatment of Ocular Inflammation Post Cataract Surgery
Started Apr 2013
50 enrolled
CataractRetinal EdemaInflammation
Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.