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NCT01868126 · ClinicalTrials.gov registry record · Phase 2
Multi-center Study Assessing the Safety and Efficacy of DE-117 Ophthalmic Solution in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 2 study, sponsored by Santen.
- Completed
- Registry status
- Phase 2
- Development phase
- 91
- Enrollment target
NCT01868126 is a Phase 2 study that has completed, run by Santen. The registered enrollment target is 91 participants.
The verdict
NCT01868126, a Phase 2 study, has completed, sponsored by Santen.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 91 participants
- Enrollment target
Study Summary
The purpose of this study is to investigate the safety and efficacy of four concentrations of DE-117 ophthalmic solution.
Interventions
- OTHER Placebo
- DRUG DE-117 ophthalmic solution
- DRUG latanoprost ophthalmic solution
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 91 participants |
| Start Date | 2013-05 |
| Est. Completion | 2013-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01868126
The ClinicalTrials.gov registry entry for NCT01868126 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 91 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Santen, which has 32 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT01868126 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01868126 about?
NCT01868126 is a clinical study titled "Multi-center Study Assessing the Safety and Efficacy of DE-117 Ophthalmic Solution in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension". The purpose of this study is to investigate the safety and efficacy of four concentrations of DE-117 ophthalmic solution.
What is the current status of trial NCT01868126?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 91 participants. The study started on 2013-05. Estimated completion is 2013-09.
What interventions are being tested in trial NCT01868126?
The interventions under investigation include: Placebo (OTHER), DE-117 ophthalmic solution (DRUG), latanoprost ophthalmic solution (DRUG).
Who is sponsoring clinical trial NCT01868126?
This trial is sponsored by Santen, which has 32 total clinical trials registered on ClinicalTrials.gov.
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