TheraRadar
Data updated: May 26, 2026

INVELTYS (loteprednol etabonate)

Pain Approved 2018-08-22

INVELTYS is indicated for the treatment of Inflammation; Pain.

Source: FDA Label • Novartis

How INVELTYS Works

Loteprednol etabonate works by binding to and activating glucocorticoid receptors to inhibit the inflammatory response. It suppresses multiple components of inflammation, including edema, fibrin deposition, capillary dilation, and leukocyte migration. It is also thought to inhibit prostaglandin production through several independent pathways. While effective at reducing inflammation and pain, the medication may delay or slow the physiological healing process.

1
Indication
--
Phase 3 Trials
7
Years on Market

Details

Status
Prescription
First Approved
2018-08-22
Patent Cliff
2033

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Routes
OPHTHALMIC
Dosage Forms
SUSPENSION/DROPS

Companies

Active Ingredient: LOTEPREDNOL ETABONATE

INVELTYS Approval History

2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
2 FDA actions from 2018 to 2020
Apr 2020 SUPPL
Label · Labeling
Aug 2018 ORIGINAL
Update · Type 5 - New Formulation or New Manufacturer

What INVELTYS Treats

2 indications

INVELTYS is approved for 2 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Inflammation
  • Pain
Source: FDA Label

INVELTYS Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

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Clinical Trial Registry

12 trials
Trial Sponsor ID Phase Status Title
NCT04555694 results posted TC-2020-DexRes Ph 4 completed Comparing Treatment of Dry Eye With Intracanalicular Dexamethasone, Restasis, and/or Lotemax
NCT01437982 628 Ph 4 completed A Study to Evaluate the Safety and Efficacy of Lotemax Ophthalmic Suspension 0.5%
NCT01443442 results posted MAC-06-11 Ph 4 completed Bepreve vs. Alrex in Subjects With Moderate to Severe Allergic Conjunctivitis
NCT01475643 results posted 670 Ph 3 completed Loteprednol vs Prednisolone for the Treatment of Intraocular Inflammation Following Cataract Surgery in Children.
NCT03098953 881 Ph 1 completed Evaluation of the Safety, Systemic Pharmacokinetics, and Tolerability of Single and Repeat Ocular Installations
NCT01853696 results posted 2013-0424 Ph 4 completed Comparison of Corticosteroid Dosing Regimens After Endothelial Keratoplasty
NCT00699153 results posted 526 Ph 3 completed Loteprednol Etabonate in an Ophthalmic Base vs Vehicle for the Treatment of Inflammation Following Cataract Surgery
NCT00705159 results posted 550 Ph 4 completed Safety and Efficacy of Zylet vs Lotemax, Tobramycin and Vehicle in Pediatric Blepharoconjunctivitis
NCT02028312 CEI.HER-002 Ph 4 withdrawn A Phase IV, Randomized, Parallel Group, Investigator-Masked Evaluation of the Effect of Loteprednol Etabonate Ophthalmic Gel 0.5% on the Initiation of Dry Eye Treatment With Restasis®
NCT01724892 othana001 Ph 4 completed Comparison the Effects of Dexamethasone and Loteprednol on Epithelial Healing
NCT01060072 results posted 577 Ph 3 completed Evaluation of Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery
NCT01010633 results posted 576 Ph 3 completed Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery
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Active Pipeline

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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.

INVELTYS FDA Label Details

Indications & Usage

FDA Label (PDF)

INVELTYS is indicated for the treatment of Inflammation; Pain.

View full patent landscape →
13 OB patents · 4 families · 93 international docs across 10 countries

INVELTYS Patents & Exclusivity

Latest Patent: May 2033

Patents (13 active)

US9056057 Expires May 3, 2033
US9532955 Expires May 3, 2033
US10058511 Expires May 3, 2033
US11219597 Expires May 3, 2033
US10864219 Expires May 3, 2033
US9737491 Expires May 3, 2033
US9827191 Expires May 3, 2033
US12115246 Expires May 3, 2033
US10688045 Expires May 3, 2033
US11642317 Expires May 3, 2033
US10646437 Expires May 3, 2033
US9393213 Expires May 3, 2033
US11872318 Expires May 3, 2033
Source: FDA Orange Book

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Revenue Insights

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Patent Timeline

  • Cliff: 2033
  • 14 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • 20 similar drugs
  • 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.