BLAINTRAVITREALINJECTABLEPriority Review
Approved
Oct 2019
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
4/8 — Partial
Priority Review
Drug data last refreshed 13h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
BEOVU (brolucizumab) is a monoclonal antibody administered via intravitreal injection for the treatment of neovascular age-related macular degeneration (AMD). It targets vascular endothelial growth factor (VEGF) to inhibit abnormal blood vessel growth in the retina. The drug represents an alternative to other anti-VEGF therapies with a potentially longer durability profile.
$0.602MPart D
PeakBEOVU is in peak commercial phase with modest Medicare utilization, suggesting a mature but focused franchise requiring specialized medical and sales expertise in ophthalmology.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Post Marketing Study to Evaluate the Safety and Effectiveness of Brolucizumab in Patients With Diabetic Macular Edema.
Started Dec 2024
66 enrolled
Diabetic Macular Edema
Brolucizumab Efficacy and Safety Single-Arm Descriptive Trial in Patients With Persistent Diabetic Macular Edema
Started Jul 2024
52 enrolled
Diabetic Macular Edema
Study Assessing the Efficacy and Safety of a Personalized Monotherapy Regimen of Brolucizumab in Patients With Symptomatic Macular Polypoidal Choroidal Vasculopathy
Started Feb 2023
148 enrolled
Macular Polypoidal Choroidal Vasculopathy (PCV)
Prospective triAl of Modified Treat-and-extend Regimens With BroLucizumab in pachychOroid Neovasculopathy
Started Jan 2023
36 enrolled
Age-Related Macular DegenerationPachychoroid Neovasculopathy
A Study to Evaluate Real-world Brolucizumab Effectiveness and Safety in Japanese Patients With Neovascular Age-related Macular Degeneration (nAMD)
Started Sep 2022
438 enrolled
Neovascular Age-Related Macular Degeneration
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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.