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NCT01558999 · ClinicalTrials.gov registry record · Phase 2
A Clinical Study Evaluating the Safety and Efficacy of SI-614 Ophthalmic Solution in Patients With Dry Eye
A Phase 2 study of Dry Eye Syndromes, sponsored by Seikagaku Corporation.
- Completed
- Registry status
- Phase 2
- Development phase
- 150
- Enrollment target
- 1
- Study location
NCT01558999: Completed Phase 2 study of Dry Eye Syndromes, sponsored by Seikagaku Corporation.
NCT01558999 is a Phase 2 study of Dry Eye Syndromes that has completed, run by Seikagaku Corporation. The registered enrollment target is 150 participants, below the 406-participant average among 17 other Dry Eye Syndromes trials with a reported enrollment target (63% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01558999, a Phase 2 study of Dry Eye Syndromes, has completed, sponsored by Seikagaku Corporation.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 150 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess the safety and effectiveness of SI-614 solution compared with placebo solution in treating patients with dry eye
Conditions Studied
Interventions
- DRUG Vehicle
- DRUG High concentration SI-614
- DRUG Low concentration SI-614
Study Locations (1)
Massachusetts
- SKK Investigational Site - Andover
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2012-03 |
| Phase | Phase 2 |
What the finished NCT01558999 record still lists
NCT01558999 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, below the 406-participant average among 17 other Dry Eye Syndromes trials with a reported enrollment target (63% lower).
The record links to 1 condition, with Dry Eye Syndromes appearing as the primary indexed condition, and to 3 interventions - of which Vehicle is the first listed.
NCT01558999 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT01558999 about?
NCT01558999 is a clinical study titled "A Clinical Study Evaluating the Safety and Efficacy of SI-614 Ophthalmic Solution in Patients With Dry Eye". The purpose of this study is to assess the safety and effectiveness of SI-614 solution compared with placebo solution in treating patients with dry eye
What is the current status of trial NCT01558999?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 150 participants. The study started on 2012-03.
What conditions does trial NCT01558999 study?
This clinical trial studies the following conditions: Dry Eye Syndromes.
What interventions are being tested in trial NCT01558999?
The interventions under investigation include: Vehicle (DRUG), High concentration SI-614 (DRUG), Low concentration SI-614 (DRUG).
Who is sponsoring clinical trial NCT01558999?
This trial is sponsored by Seikagaku Corporation, which has 12 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01558999 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Dry Eye Syndromes
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01558999's enrollment target sits among peer trials
150 8th of 17 higher than 10 of 17 other Dry Eye Syndromes trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Dry Eye Syndromes 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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A Clinical Study Evaluating the Safety and Efficacy of SI-614 Ophthalmic Solution in Patients With Dry Eye.
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