TheraRadar

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Data updated: Mar 10, 2026

COSOPT

DORZOLAMIDE HYDROCHLORIDE
Cardiovascular Approved 1998-04-07
1
Indication
--
Phase 3 Trials
27
Years on Market

Details

Status
Prescription
First Approved
1998-04-07
Routes
OPHTHALMIC
Dosage Forms
SOLUTION/DROPS

Companies

COSOPT Approval History

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What COSOPT Treats

2 indications

COSOPT is approved for 2 conditions since its original approval in 1998. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Glaucoma
  • Ocular Hypertension
Source: FDA Label

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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.

COSOPT FDA Label Details

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Indications & Usage

FDA Label (PDF)

COSOPT ® is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension who are insufficiently responsive to beta-blockers (failed to achieve target IOP determined after multiple measurements over time). The IOP-lowering of COSOPT administered twice a day was slightly less than that seen with the concomitant administration of 0.5% timolol administered twice a day and 2% dorzolamide administered three times a day [see Clinical Studies ] . COSOPT is a combination of dorzolamide hydrochloride, a carbonic anhydrase inhibitor, and t...

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Data Sources

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