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NCT01257607 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy Study of MIM-D3 Ophthalmic Solution for the Treatment of Dry Eye
A Phase 2 study, sponsored by Mimetogen Pharmaceuticals USA.
- Completed
- Registry status
- Phase 2
- Development phase
- 150
- Enrollment target
NCT01257607: Completed Phase 2 study, sponsored by Mimetogen Pharmaceuticals USA.
NCT01257607 is a Phase 2 study that has completed, run by Mimetogen Pharmaceuticals USA. The registered enrollment target is 150 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (13% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01257607, a Phase 2 study, has completed, sponsored by Mimetogen Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 150 participants
- Enrollment target
Study Summary
The objective of this study is to compare the safety and efficacy of 1% MIM-D3 and 5% MIM-D3 to placebo for the treatment of the signs and symptoms of dry eye.
Primary Outcome
Ocular surface damage
Interventions
- DRUG Placebo Ophthalmic Solution
- DRUG MIM-D3 Ophthalmic Solution
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2010-11 |
| Est. Completion | 2011-05 |
| Phase | Phase 2 |
What the finished NCT01257607 record still lists
NCT01257607 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, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (13% higher).
The record links to 0 conditions, and to 2 interventions - of which Placebo Ophthalmic Solution is the first listed.
NCT01257607 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01257607 about?
NCT01257607 is a clinical study titled "Safety and Efficacy Study of MIM-D3 Ophthalmic Solution for the Treatment of Dry Eye". The objective of this study is to compare the safety and efficacy of 1% MIM-D3 and 5% MIM-D3 to placebo for the treatment of the signs and symptoms of dry eye.
What is the current status of trial NCT01257607?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 150 participants. The study started on 2010-11. Estimated completion is 2011-05.
What interventions are being tested in trial NCT01257607?
The interventions under investigation include: Placebo Ophthalmic Solution (DRUG), MIM-D3 Ophthalmic Solution (DRUG).
Who is sponsoring clinical trial NCT01257607?
This trial is sponsored by Mimetogen Pharmaceuticals USA, which has 6 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01257607's enrollment target sits among peer trials
150 455th of 2000 higher than 1,510 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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