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Safety Study of Ophthalmic Solution in Healthy, Normal Volunteers
NCT00223951 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the safety of R89674 0.25% ophthalmic solution in healthy normal volunteers
Conditions Studied
Interventions
- DRUG R89674 (generic name not yet established)
Study Locations (6)
Arizona
- — Phoenix
Maryland
- — Bel Air
Massachusetts
- — North Andover
Nevada
- — Las Vegas
North Carolina
- — Charlotte
Pennsylvania
- — Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 900 participants |
| Start Date | 2005-09 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00223951
The ClinicalTrials.gov registry entry for NCT00223951 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 900 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vistakon Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Healthy Volunteers Eligible for Study; Drug Being Developed for Allergic Conjunctivitis appearing as the primary indexed condition, and to 1 intervention — of which R89674 (generic name not yet established) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00223951 reports 6 study locations spanning 6 distinct geographic areas — top geographies include Arizona, Maryland, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00223951 about?
NCT00223951 is a clinical study titled "Safety Study of Ophthalmic Solution in Healthy, Normal Volunteers". The purpose of this study is to evaluate the safety of R89674 0.25% ophthalmic solution in healthy normal volunteers
What is the current status of trial NCT00223951?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 900 participants. The study started on 2005-09.
What conditions does trial NCT00223951 study?
This clinical trial studies the following conditions: Healthy Volunteers Eligible for Study; Drug Being Developed for Allergic Conjunctivitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00223951?
The interventions under investigation include: R89674 (generic name not yet established) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00223951?
This trial is sponsored by Vistakon Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00223951 being conducted?
This trial has 6 study locations across Arizona, Maryland, Massachusetts, Nevada, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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