DE-111 ophthalmic solution + Tafluprost ophthalmic solution 0.0015% + Concomitant use of tafluprost ophthalmic solution 0.0015% plus timolol ophthalmic solution 0.5%

Phase 3Completed
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77
Hype Score

Development Stage

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

Open Angle Glaucoma

Conditions

Open Angle Glaucoma, Ocular Hypertension

Trial Timeline

May 1, 2011 โ†’ โ€”

About DE-111 ophthalmic solution + Tafluprost ophthalmic solution 0.0015% + Concomitant use of tafluprost ophthalmic solution 0.0015% plus timolol ophthalmic solution 0.5%

DE-111 ophthalmic solution + Tafluprost ophthalmic solution 0.0015% + Concomitant use of tafluprost ophthalmic solution 0.0015% plus timolol ophthalmic solution 0.5% is a phase 3 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 NCT01342081. Target conditions include Open Angle Glaucoma, Ocular Hypertension.

Hype Score Breakdown

Clinical
27
Activity
18
Company
10
Novelty
9
Community
10

Clinical Trials (1)

NCT IDPhaseStatus
NCT01342081Phase 3Completed