0.01% RO7058584 + 0.1% RO7058584 + 1% RO7058584 + Matching Placebo + Latanoprost 0.005%

Phase 1Completed
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33
Hype Score

Development Stage

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

Glaucoma, Open-angle

Conditions

Glaucoma, Open-angle, Ocular Hypertension

Trial Timeline

Oct 10, 2017 โ†’ Dec 21, 2017

About 0.01% RO7058584 + 0.1% RO7058584 + 1% RO7058584 + Matching Placebo + Latanoprost 0.005%

0.01% RO7058584 + 0.1% RO7058584 + 1% RO7058584 + Matching Placebo + Latanoprost 0.005% is a phase 1 stage product being developed by Roche for Glaucoma, Open-angle. The current trial status is completed. This product is registered under clinical trial identifier NCT03293992. Target conditions include Glaucoma, Open-angle, Ocular Hypertension.

Hype Score Breakdown

Clinical
10
Activity
5
Company
10
Novelty
3
Community
2

Clinical Trials (1)

NCT IDPhaseStatus
NCT03293992Phase 1Completed

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SDP-133 + LumiganSun PharmaceuticalPhase 3
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23
DE-117B Eye Drops + LatanoprostSanten PharmaceuticalPhase 3
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77
DE-111 ophthalmic solutionSanten PharmaceuticalPhase 3
77
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77
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52
DE-117 ophthalmic solution + Latanoprost ophthalmic solution 0.005%Santen PharmaceuticalPhase 3
77
STN1012600 ophthalmic solution 0.002% + Latanoprost ophthalmic solution 0.005%Santen PharmaceuticalPhase 3
77
DE-117 + Latanoprost ophthalmic solutionSanten PharmaceuticalPhase 3
77
DE-117 ophthalmic solution + Timolol ophthalmic solutionSanten PharmaceuticalPhase 3
77
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
77
Placebo ophthalmic solution + DE-117 ophthalmic solution low + DE-117 ophthalmic solution high + Latanoprost ophthalmic solution 0.005%Santen PharmaceuticalPhase 2/3
65