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NCT00404885 · ClinicalTrials.gov registry record · Phase 3
A Multi-center Study to Assess the Efficacy and Safety of LX211 in Active Non-infectious Anterior Uveitis
A Phase 3 study of Uveitis, Anterior and Panuveitis, sponsored by Lux Biosciences.
- Completed
- Registry status
- Phase 3
- Development phase
- 108
- Enrollment target
- 20
- Study locations
NCT00404885: Completed Phase 3 study of Uveitis, Anterior and Panuveitis, sponsored by Lux Biosciences.
NCT00404885 is a Phase 3 study of Uveitis, Anterior and Panuveitis that has completed, run by Lux Biosciences. The registered enrollment target is 108 participants, above the 61-participant average among 4 other Uveitis, Anterior trials with a reported enrollment target (77% higher). The trial reports 20 study locations across 14 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00404885, a Phase 3 study of Uveitis, Anterior and Panuveitis, has completed, sponsored by Lux Biosciences.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 108 participants
- Enrollment target
- 20
- Study locations
Study Summary
The objective of this study is to evaluate the safety and efficacy of LX211 as therapy in subjects with active non-infectious anterior uveitis
Conditions Studied
Interventions
- DRUG Placebo
- DRUG LX211
Study Locations (20)
Other
- Universitätsklinik für Augenheilkunde - Salzburg
- Klinik für Augenheilkunde, Dept. of Ophthalmology - Vienna
- Hôpital Pitié Salpétrière, Service d'Ophtalmologie - Paris
- Universitätsklinikum Freiburg - Freiburg im Breisgau
- Augenklinik der Universität Heidelberg - Heidelberg
Massachusetts
- Massachusetts Eye and Ear Infirmary - Boston
- Massachusetts Eye Research and Surgery Institute - Cambridge
Texas
- Brian B. Berger, MD, P.A. - Austin
- Retina & Uveitis Consultants of Texas - San Antonio
Alabama
- University of Alabama at Birmingham - Birmingham
Arizona
- Retinal Consultants of Arizona - Phoenix
Illinois
- University of Illinois - Chicago - Chicago
Maryland
- Wilmer Eye Institute - Baltimore
Michigan
- Associated Retinal Consultants, PC - Grand Rapids
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 108 participants |
| Start Date | 2007-01 |
| Est. Completion | 2009-05 |
| Phase | Phase 3 |
What the finished NCT00404885 record still lists
NCT00404885 is an interventional study that assigns participants to a tested intervention. The registered 108 participants enrollment target is mid-sized for trials with a published cap, above the 61-participant average among 4 other Uveitis, Anterior trials with a reported enrollment target (77% higher).
The record links to 2 conditions, with Uveitis, Anterior appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT00404885 names 20 study sites across 14 states, led by Other, Massachusetts, Texas.
Frequently Asked Questions
What is clinical trial NCT00404885 about?
NCT00404885 is a clinical study titled "A Multi-center Study to Assess the Efficacy and Safety of LX211 in Active Non-infectious Anterior Uveitis". The objective of this study is to evaluate the safety and efficacy of LX211 as therapy in subjects with active non-infectious anterior uveitis
What is the current status of trial NCT00404885?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 108 participants. The study started on 2007-01. Estimated completion is 2009-05.
What conditions does trial NCT00404885 study?
This clinical trial studies the following conditions: Uveitis, Anterior, Panuveitis.
What interventions are being tested in trial NCT00404885?
The interventions under investigation include: Placebo (DRUG), LX211 (DRUG).
Who is sponsoring clinical trial NCT00404885?
This trial is sponsored by Lux Biosciences, which has 7 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00404885 being conducted?
This trial has 20 study locations across Alabama, Arizona, Illinois, Maryland, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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