TheraRadar
Data updated: May 26, 2026

LUMIFY (brimonidine tartrate)

Ophthalmology Approved 2017-12-22
1
Indication
--
Phase 3 Trials
8
Years on Market

Details

Status
Over-the-counter
First Approved
2017-12-22
Patent Cliff
2030

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Routes
OPHTHALMIC
Dosage Forms
SOLUTION/DROPS

Companies

Active Ingredient: BRIMONIDINE TARTRATE

LUMIFY Approval History

2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
8 FDA actions from 2017 to 2024
Feb 2024 SUPPL
Label · Labeling
May 2023 SUPPL
Mfg · Manufacturing (CMC)
Nov 2021 SUPPL
Label · Labeling

What LUMIFY Treats

1 FDA approvals

Originally approved for its first indication in 2017 .

  • Other (1)
📋

Clinical Trial Registry

12 trials
Trial Sponsor ID Phase Status Title
NCT05270863 results posted VT-002 Ph 3 completed Safety and Efficacy Study BRIMOCHOL™ PF and Carbachol PF in Subjects With Emmetropic Phakic or Pseudophakic Presbyopia
NCT03785340 results posted OCU-310-301 Ph 3 completed Study of Brimonidine Tartrate Nanoemulsion Eye Drop Solution in the Treatment of Dry Eye Disease (DED)
NCT03591874 oGVHD results posted OCU-300-301 Ph 3 terminated Study of Brimonidine Tartrate Nanoemulsion Eye Drops in Patients With Ocular Graft-vs-Host Disease
NCT03760185 results posted 18-1713 Ph 2 completed Pupil Dilation for Treatment of IFIS
NCT03323164 results posted 17-636E Ph 4 completed Peripapillary Blood Flow After Use of Anti-glaucoma Medications: An OCT Angiography Study
NCT01959230 results posted 861 Ph 3 completed Efficacy and Safety of Brimonidine Tartrate Ophthalmic Solution in Adult and Geriatric Participants With Ocular Redness
NCT01959243 results posted 862 Ph 3 completed Safety of Brimonidine Tartrate Ophthalmic Solution in a Population of Pediatric, Adult, and Geriatric Participants
NCT03966560 KAEK-2014/04-74 Ph 4 completed Choroidal Thickness and Its Correlations With Ocular Parameters in Primary Open-angle Glaucoma
NCT03173365 BRIMOCAN BRIMOCAN Ph 2 terminated The Effect of Topical Brimonidine Tartrate on Hand-foot Syndrome (HFS) in Cancer Patients
NCT02039765 863/13-100-0007 Ph 1 completed Pharmacokinetics and Safety of Topical Administration of Brimonidine Tartrate Ophthalmic Solution 0.025%.
NCT02856919 BR14004 BR.14.004 Ph 4 completed A Multicenter, Open-label Clinical Trial to Evaluate the Efficacy and Safety of Once Daily Mirvaso® Gel in Patients With Chronic Persistent Vascular Facial Erythema.
NCT02568111 BRITE NLD-PEG-14-10784 2015-002159-89 Ph 4 withdrawn Brimonidine Tartrate for the Treatment of Injection Related Erythema
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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📊

Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

LUMIFY FDA Label Details

View full patent landscape →
4 OB patents · 2 families · 53 international docs across 14 countries

LUMIFY Patents & Exclusivity

Latest Patent: Jul 2030

Patents (4 active)

US8293742 Expires Jul 14, 2030
US9259425 Expires Jul 14, 2030
US11596600 Expires Jul 27, 2029
US11833245 Expires Jul 27, 2029
Source: FDA Orange Book

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Revenue Insights

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  • Historical trend analysis

Patent Timeline

  • Cliff: 2030
  • 4 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • Competitor tracking
  • Same target/indication analysis
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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.