TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ACUVUE THERAVISION WITH KETOTIFEN

KETOTIFEN FUMARATE
Approved 2022-02-25
1
Indication
--
Phase 3 Trials
4
Years on Market

Details

Status
Discontinued
First Approved
2022-02-25
Routes
OPHTHALMIC
Dosage Forms
DRUG-ELUTING CONTACT LENS

Companies

Active Ingredient: KETOTIFEN FUMARATE

ACUVUE THERAVISION WITH KETOTIFEN Approval History

Loading approval history...

What ACUVUE THERAVISION WITH KETOTIFEN Treats

1 FDA approvals

Originally approved for its first indication in 2022 .

  • Other (1)
๐Ÿ”ฌ

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...
โญ

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
๐Ÿ“Š

Trial Timeline

Full development history with FDA approval milestones

Loading...
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.

ACUVUE THERAVISION WITH KETOTIFEN FDA Label Details

Pro

ACUVUE THERAVISION WITH KETOTIFEN Patents & Exclusivity

Latest Patent: Jun 2030

Patents (2 active)

US9962376 Expires Jun 27, 2030
US9474746 Expires Mar 27, 2028
Source: FDA Orange Book

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

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