DE-104 ophthalmic solution + DE-104 vehicle

Phase 2Completed
0 views this week 0 watching💤 Quiet
Interest: 35/100
35
Hype Score

Development Stage

Pre-clinical
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Open-Angle Glaucoma

Conditions

Open-Angle Glaucoma, Ocular Hypertension

Trial Timeline

— → —

About DE-104 ophthalmic solution + DE-104 vehicle

DE-104 ophthalmic solution + DE-104 vehicle is a phase 2 stage product being developed by Santen Pharmaceutical for Open-Angle Glaucoma. The current trial status is completed. This product is registered under clinical trial identifier NCT00656240. Target conditions include Open-Angle Glaucoma, Ocular Hypertension.

Hype Score Breakdown

Clinical
12
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT00656240Phase 2Completed

Competing Products

20 competing products in Open-Angle Glaucoma

See all competitors
ProductCompanyStageHype Score
Test - Bimatoprost 0.01% Ophthalmic Solution + Reference - LUMIGAN® (Bimatoprost 0.01% Ophthalmic Solution)Mankind PharmaPhase 3
40
DE-104 ophthalmic solution, low concentration + DE-104 ophthalmic solution, medium concentration + DE-104 ophthalmic solution, high concentration + DE-104 vehicleSanten PharmaceuticalPhase 2
35
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
Bimatoprost SRAbbViePhase 3
44
Bimatoprost SR + LUMIGANAbbViePhase 3
40
AGN-193408 SR + AGN-193408 SRAbbViePhase 1/2
39
Bimatoprost (SR)AbbViePhase 3
40
Bimatoprost Sustained Release ImplantAbbViePre-clinical
26
Bimatoprost SR + Sham Bimatoprost SRAbbViePhase 3
40
Preservative-Free Tafluprost + Comparator: timololMerckPhase 3
40
Brinzolamide 1%/Timolol maleate 0.5% fixed combination ophthalmic suspension + Dorzolamide hydrochloride 1%/Timolol maleate 0.5% ophthalmic solution + Subject's habitual PGA monotherapyNovartisApproved
43
Placebo + RO5093151RochePhase 2
35
0.01% RO7058584 + 0.1% RO7058584 + 1% RO7058584 + Matching Placebo + Latanoprost 0.005%RochePhase 1
29
XalacomPfizerPhase 3
40
XalatanPfizerPhase 2
27
LatanoprostPfizerApproved
43
PF-04217329 - Lowest Dose + PF-04217329 - Low Dose + PF-04217329 - Middle Dose + PF-04217329 - High Middle Dose + PF-04217329 - High Dose + PF-4217329 - Highest Dose + PF-04217329 - Vehicle + Latanoprost Vehicle + PF-04217329 - Low Dose + Latanoprost Vehicle + PF-04217329 - Middle Dose + Latanoprost Vehicle + PF-04217329 - High Dose + Latanoprost 0.005% + PF-04217329 - Low Dose + Latanoprost 0.005% + PF-04217329 - Middle Dose + Latanoprost 0.005% + PF-04217329 - High Dose + Latanoprost 0.005% + PF-04217329 - VehiclePfizerPhase 2
35
XalacomPfizerPre-clinical
26
Xalacom + Xalatan + TimololPfizerPhase 3
40
PF-04217329 + latanoprost vehicle + PF-04217329 + latanoprostPfizerPhase 2
35