Clinical trial
A Multi-center Study to Assess the Efficacy and Safety of LX211 in Active…
NCT00404885 · Lux Biosciences, Inc., Industry · Completed
Key facts
| NCT number | NCT00404885 |
|---|---|
| Title | A Multi-center Study to Assess the Efficacy and Safety of LX211 in Active Non-infectious Anterior Uveitis |
| Official title | A Double-Masked, Placebo-Controlled, Parallel-Group, Multi-Center, Dose-Ranging Study With an Optional Extension to Assess the Efficacy and Safety of LX211 as Therapy in Subjects With Active Sight Threatening, Non-infectious Anterior Uveitis |
| Acronym | LUMINATE |
| Lead sponsor | Lux Biosciences, Inc., Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Uveitis, Anterior, Panuveitis |
| Intervention type | Drug |
| Interventions | Placebo, LX211 |
| Enrollment | 108 |
| Start date | Jan 1, 2007 |
| Primary completion | Nov 1, 2008 |
| Completion | May 1, 2009 |
| First posted | Nov 29, 2006 |
| Last update posted | Jun 22, 2012 |
| Countries | Austria, Canada, France, Germany, India, United Kingdom, United States |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: