latanoprost 0.005% (Xalatan)

ApprovedCompleted
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Interest: 43/100
43
Hype Score

Development Stage

Pre-clinical
Phase 1
Phase 2
Phase 3
5
Approved
Indication / Disease

Ocular Hypertension

Conditions

Ocular Hypertension, Glaucoma, Open-Angle

Trial Timeline

Feb 1, 2002 → Apr 1, 2006

About latanoprost 0.005% (Xalatan)

latanoprost 0.005% (Xalatan) is a approved stage product being developed by Pfizer for Ocular Hypertension. The current trial status is completed. This product is registered under clinical trial identifier NCT00140062. Target conditions include Ocular Hypertension, Glaucoma, Open-Angle.

What happened to similar drugs?

3 of 20 similar drugs in Ocular Hypertension were approved

Approved (3) Terminated (0) Active (17)

Hype Score Breakdown

Clinical
20
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT00140062ApprovedCompleted

Competing Products

20 competing products in Ocular Hypertension

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ProductCompanyStageHype Score
lotilaner + VehicleTarsus PharmaceuticalsPhase 2
36
Mirabegron + PlaceboAstellas PharmaPhase 1
29
ISV-303 + ISV-303 + DuraSite Vehicle + Xibrom™Sun PharmaceuticalPhase 1/2
32
ISV-303Sun PharmaceuticalPhase 3
40
ISV-303Sun PharmaceuticalPhase 3
40
ONO-9054 + LatanoprostOno PharmaceuticalPhase 2
35
ONO-9054 + PlaceboOno PharmaceuticalPhase 1
29
STN1012600 ophthalmic solution 0.002% + STN1012600 ophthalmic solution 0.002% + STN1012600 ophthalmic solution 0.002% and Timolol ophthalmic solution 0.5%Santen PharmaceuticalPhase 3
40
Tafluprost, timolol maleateSanten PharmaceuticalPre-clinical
26
DE-111 ophthalmic solutionSanten PharmaceuticalPhase 3
40
DE-117 ophthalmic solution + Latanoprost ophthalmic solution 0.005%Santen PharmaceuticalPhase 3
40
STN1012600 ophthalmic solution 0.002% + Latanoprost ophthalmic solution 0.005%Santen PharmaceuticalPhase 3
40
DE-117 + Latanoprost ophthalmic solutionSanten PharmaceuticalPhase 3
40
DE-117 ophthalmic solution + Timolol ophthalmic solutionSanten PharmaceuticalPhase 3
40
A preservative-free, a clear, colorless sterile aqueous ophthalmic solution containing 0.015mg of tafluprost and 5.0mg of timolol in 1mL + A preservative-free, a clear, colorless sterile aqueous ophthalmic solution containing 0.015mg of tafluprost in 1mLSanten PharmaceuticalPhase 3
40
Omaveloxolone Ophthalmic Suspension 1.0% + Omaveloxolone Opthalmic Suspension 0.5% + PlaceboAbbViePhase 2
35
AZD4017 + Placebo + AZD4017 + PlaceboAstraZenecaPhase 2
35
dorzolamide hydrochloride (+) timolol maleateMerckApproved
43
INS115644 Ophthalmic Solution + Placebo + INS115644 Ophthalmic Solution + INS115644 Ophthalmic Solution + INS115644 Ophthalmic SolutionMerckPhase 1
29
SAD448NovartisPhase 1
29