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NCT00241319 · ClinicalTrials.gov registry record · Phase 3
Evaluation of Efficacy of Ophthalmic Solution in Induced Acute Allergic Conjunctivitis
A Phase 3 study, sponsored by Vistakon Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 150
- Enrollment target
NCT00241319: Completed Phase 3 study, sponsored by Vistakon Pharmaceuticals.
NCT00241319 is a Phase 3 study that has completed, run by Vistakon Pharmaceuticals. The registered enrollment target is 150 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00241319, a Phase 3 study, has completed, sponsored by Vistakon Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 150 participants
- Enrollment target
Study Summary
The purpose of this study is to establish the efficacy of R89674 0.25% ophthalmic solution compared with placebo in alleviating the signs and symptoms of conjunctival allergen challenge-induced allergic conjunctivitis
Interventions
- DRUG R89674 (generic name not yet established)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2005-10 |
| Phase | Phase 3 |
What the finished NCT00241319 record still lists
NCT00241319 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 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 1 intervention - of which R89674 (generic name not yet established) is the first listed.
NCT00241319 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00241319 about?
NCT00241319 is a clinical study titled "Evaluation of Efficacy of Ophthalmic Solution in Induced Acute Allergic Conjunctivitis". The purpose of this study is to establish the efficacy of R89674 0.25% ophthalmic solution compared with placebo in alleviating the signs and symptoms of conjunctival allergen challenge-induced allergic conjunctivitis
What is the current status of trial NCT00241319?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 150 participants. The study started on 2005-10.
What interventions are being tested in trial NCT00241319?
The interventions under investigation include: R89674 (generic name not yet established) (DRUG).
Who is sponsoring clinical trial NCT00241319?
This trial is sponsored by Vistakon Pharmaceuticals, which has 13 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00241319's enrollment target sits among peer trials
150 1519th of 2000 higher than 455 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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