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NCT02078661 · ClinicalTrials.gov registry record · Phase 1
Safety and Efficacy of PG101 for Dry Eye Syndrome
A Phase 1 study, sponsored by Rhodes Pharmaceuticals, L.P..
- Completed
- Registry status
- Phase 1
- Development phase
- 72
- Enrollment target
NCT02078661: Completed Phase 1 study, sponsored by Rhodes Pharmaceuticals, L.P..
NCT02078661 is a Phase 1 study that has completed, run by Rhodes Pharmaceuticals, L.P.. The registered enrollment target is 72 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02078661, a Phase 1 study, has completed, sponsored by Rhodes Pharmaceuticals, L.P..
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 72 participants
- Enrollment target
Study Summary
To evaluate the safety and efficacy of 0.25% PG101 and 1.0% PG101 topical gel suspension compared to placebo when administered two times daily for 14 days in subjects diagnosed with dry eye syndrome
Primary Outcome
Dry eye ocular symptoms measured are: Ocular discomfort, dryness, grittiness, burning, stinging, photophobia, lid friction, mucus discharge and hyper-tearing.
Interventions
- DRUG PG101
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2013-12 |
| Est. Completion | 2014-01 |
| Phase | Phase 1 |
What the finished NCT02078661 record still lists
NCT02078661 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher).
The record links to 0 conditions, and to 1 intervention - of which PG101 is the first listed.
NCT02078661 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02078661 about?
NCT02078661 is a clinical study titled "Safety and Efficacy of PG101 for Dry Eye Syndrome". To evaluate the safety and efficacy of 0.25% PG101 and 1.0% PG101 topical gel suspension compared to placebo when administered two times daily for 14 days in subjects diagnosed with dry eye syndrome
What is the current status of trial NCT02078661?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 72 participants. The study started on 2013-12. Estimated completion is 2014-01.
What interventions are being tested in trial NCT02078661?
The interventions under investigation include: PG101 (DRUG).
Who is sponsoring clinical trial NCT02078661?
This trial is sponsored by Rhodes Pharmaceuticals, L.P., which has 10 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02078661's enrollment target sits among peer trials
72 736th of 2000 higher than 1,254 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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