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NCT01917383 · ClinicalTrials.gov registry record · Phase 2
A Phase II Study to Evaluate the Additivity of Trabodenoson to Latanoprost in Adults With Ocular Hypertension or Primary Open-Angle Glaucoma
A Phase 2 study, sponsored by Inotek Pharmaceuticals Corporation.
- Completed
- Registry status
- Phase 2
- Development phase
- 101
- Enrollment target
NCT01917383: Completed Phase 2 study, sponsored by Inotek Pharmaceuticals Corporation.
NCT01917383 is a Phase 2 study that has completed, run by Inotek Pharmaceuticals Corporation. The registered enrollment target is 101 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (24% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01917383, a Phase 2 study, has completed, sponsored by Inotek Pharmaceuticals Corporation.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 101 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the intraocular pressure (IOP) lowering efficacy and the safety and tolerability profile of trabodenoson ophthalmic formulation compared to timolol maleate ophthalmic solution 0.5% in adults with ocular hypertension (OHT) or primary open-angle glaucoma (POAG) who are already receiving treatment with latanoprost ophthalmic solution 0.005% once every evening (QPM).
Interventions
- DRUG Latanoprost
- DRUG Timolol
- DRUG Trabodenoson
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 101 participants |
| Start Date | 2013-08 |
| Est. Completion | 2014-09 |
| Phase | Phase 2 |
What the finished NCT01917383 record still lists
NCT01917383 is an interventional study that assigns participants to a tested intervention. The registered 101 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (24% lower).
The record links to 0 conditions, and to 3 interventions - of which Latanoprost is the first listed.
NCT01917383 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01917383 about?
NCT01917383 is a clinical study titled "A Phase II Study to Evaluate the Additivity of Trabodenoson to Latanoprost in Adults With Ocular Hypertension or Primary Open-Angle Glaucoma". The purpose of this study is to evaluate the intraocular pressure (IOP) lowering efficacy and the safety and tolerability profile of trabodenoson ophthalmic formulation compared to timolol maleate ophthalmic solution 0.5% in adults with ocular hypertension (OHT) or primary open-angle glaucoma (POAG)...
What is the current status of trial NCT01917383?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 101 participants. The study started on 2013-08. Estimated completion is 2014-09.
What interventions are being tested in trial NCT01917383?
The interventions under investigation include: Latanoprost (DRUG), Timolol (DRUG), Trabodenoson (DRUG).
Who is sponsoring clinical trial NCT01917383?
This trial is sponsored by Inotek Pharmaceuticals Corporation, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01917383's enrollment target sits among peer trials
101 672nd of 2000 higher than 1,329 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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