TheraRadar
Data updated: May 26, 2026

TRAVATAN Z (travoprost)

Trial Activity: Mature
Ophthalmology Approved 2006-09-21

Travatan Z is an ophthalmic solution used for patients who have elevated pressure inside their eyes. It treats conditions such as open-angle glaucoma and ocular hypertension by lowering intraocular pressure. This medication helps patients with these conditions manage their eye health and reduce the risks associated with high internal eye pressure.

Source: FDA Label • Novartis • Prostaglandin Analog

How TRAVATAN Z Works

This medication works by acting as a selective FP prostanoid receptor agonist. It is believed to lower eye pressure by increasing the uveoscleral outflow of fluid from the eye. While the exact mechanism is not fully understood, this increased drainage effectively reduces intraocular pressure.

Development Insights

Wills Eye conducting 1 trials (33%)
4 indications explored (Focused)
glaucoma (2 trials)
ocular hypertension (1 trials)
ocular surface disease (1 trials)
2
Indications
--
Phase 3 Trials
19
Years on Market

Details

Status
Prescription
First Approved
2006-09-21
Patent Cliff
2029

Pro Metrics

Patent cliff and revenue data

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Routes
OPHTHALMIC
Dosage Forms
SOLUTION/DROPS

Companies

Active Ingredient: TRAVOPROST

TRAVATAN Z Approval History

2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
7 FDA actions from 2006 to 2025 · 1 indication expansions
Oct 2025 SUPPL
Label · Labeling
Apr 2020 SUPPL
Label · Labeling
Sep 2017 SUPPL
Label · Labeling

What TRAVATAN Z Treats

2 indications

TRAVATAN Z is approved for 2 conditions since its original approval in 2006. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Glaucoma
  • Ocular Hypertension
Source: FDA Label

TRAVATAN Z Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

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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.

Drugs Similar to TRAVATAN Z

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LEVOBUNOLOL HYDROCHLORIDE
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Shared indications:
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Shared indications:
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Clinical Trial Registry

11 trials
Trial Sponsor ID Phase Status Title
NCT02390284 STOP-RGCD results posted 20140587 R01EY014957 Ph 3 terminated Stop Retinal Ganglion Cell Dysfunction Study
NCT04615403 results posted IDOS-106-EXCH Ph 2 completed Study of Exchange of Travoprost Intraocular Implant
NCT01444040 GCF-027 Ph 4 completed Subjects With Open-angle Glaucoma, Pseudoexfoliative Glaucoma, or Ocular Hypertension Naïve to Medical and Surgical Therapy, Treated With Two Trabecular Micro-bypass Stents (iStent Inject) or Travoprost
NCT02914509 results posted OTX-16-002 Ph 3 completed Phase 3 Study Evaluating Safety and Efficacy of OTX-TP in Subjects With OAG or OHT
NCT00798694 results posted 08-875 Ph 4 completed How Similar Are Changes to the Surface of the Eye When Two Different Glaucoma Eye Drops Are Used?
NCT01443988 GCF-022 Ph 4 completed Subjects With Open-angle Glaucoma, Pseudoexfoliative Glaucoma, or Ocular Hypertension Naïve to Medical and Surgical Therapy, Treated With Two Trabecular Micro-bypass Stents (iStent)or Travoprost
NCT01315574 BAK results posted 11-007H Ph 4 terminated Effects of Anti-Glaucoma Medications on the Ocular Surface
NCT02105311 EC57-020-02-1 Ph 4 completed Effect of Selective Laser Trabeculoplasty Versus Travoprost on Circardian Intraocular Pressure
NCT01254370 NVG10E118 Ph 2 completed Safety and Efficacy Study of Catioprost® (Unpreserved Latanoprost 0.005% Emulsion) Compared to Travatan Z® to Treat Glaucoma and Ocular Surface Disease
NCT00705757 results posted Pfizer GA6111AX Ph 4 completed The Effects of Xalatan, Travatan and Lumigan on Skin Pigmentation Near the Eye
NCT00799682 GA6111ZH Ph 4 completed Exploratory Study Comparing Signs and Symptoms in Patients With Ocular Hypertension or Glaucoma Using Xalatan R® or Travatan Z®
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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.

TRAVATAN Z FDA Label Details

Indications & Usage

FDA Label (PDF)

TRAVATAN Z is indicated for the treatment of Glaucoma; Ocular Hypertension.

View full patent landscape →
3 OB patents · 2 families · 66 international docs across 24 countries

TRAVATAN Z Patents & Exclusivity

Latest Patent: Oct 2029

Patents (3 active)

US8268299 Expires Oct 13, 2029
US8323630 Expires Sep 20, 2027
US8388941 Expires Sep 20, 2027
Source: FDA Orange Book

Pro Intelligence Preview

Deep insights for TRAVATAN Z

Revenue Insights

  • Quarterly revenue tracking
  • Historical trend analysis

Patent Timeline

  • Cliff: 2029
  • 3 active patents

Trial Analysis

  • 3 total trials
  • Stage: Mature

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.

How We Calculate These Metrics

Trial Activity Stage

Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.

Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.

  • Growth: High proportion of early-phase trials (Phase 1/2), active development
  • Expansion: Significant Phase 3 activity, approaching or pursuing approvals
  • Mature: Substantial Phase 4 post-marketing studies
  • Stable: Mixed phase distribution, steady development
  • Declining: Low active trial ratio, reduced R&D investment