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NCT00244543 · ClinicalTrials.gov registry record · Phase 3
Evaluation of Efficacy of Ophthalmic Solution in Induced Allergic Conjunctivitis
A Phase 3 study of Allergic Conjunctivitis, sponsored by Vistakon Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 110
- Enrollment target
- 1
- Study location
NCT00244543 is a Phase 3 study of Allergic Conjunctivitis that has completed, run by Vistakon Pharmaceuticals. The registered enrollment target is 110 participants, below the 129-participant average among 20 other Allergic Conjunctivitis trials with a reported enrollment target (15% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00244543, a Phase 3 study of Allergic Conjunctivitis, has completed, sponsored by Vistakon Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 110 participants
- Enrollment target
- 1
- Study location
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
Conditions Studied
Interventions
- DRUG R89674 (generic name not yet established)
Study Locations (1)
Massachusetts
- - North Andover
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2005-10 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00244543
The ClinicalTrials.gov registry entry for NCT00244543 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 129-participant average among 20 other Allergic Conjunctivitis trials with a reported enrollment target (15% lower). The listed sponsor is Vistakon Pharmaceuticals, which has 13 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Allergic Conjunctivitis appearing as the primary indexed condition, and to 1 intervention - of which R89674 (generic name not yet established) is the first listed.
NCT00244543 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT00244543 about?
NCT00244543 is a clinical study titled "Evaluation of Efficacy of Ophthalmic Solution in Induced 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 NCT00244543?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 110 participants. The study started on 2005-10.
What conditions does trial NCT00244543 study?
This clinical trial studies the following conditions: Allergic Conjunctivitis.
What interventions are being tested in trial NCT00244543?
The interventions under investigation include: R89674 (generic name not yet established) (DRUG).
Who is sponsoring clinical trial NCT00244543?
This trial is sponsored by Vistakon Pharmaceuticals, which has 13 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00244543 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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