Clinical trial
Anecortave Acetate Risk-Reduction Trial (AART)
NCT00307398 · Alcon Research, Industry · Terminated
Key facts
| NCT number | NCT00307398 |
|---|---|
| Title | Anecortave Acetate Risk-Reduction Trial (AART) |
| Lead sponsor | Alcon Research, Industry |
| Status | Terminated |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Dry AMD |
| Intervention type | Drug, Other |
| Interventions | Anecortave Acetate (AL-3789) sterile suspension, 15 mg or 30 mg, Anecortave Acetate Vehicle |
| Enrollment | 2,596 |
| Start date | Mar 1, 2004 |
| Primary completion | Jan 1, 2009 |
| Completion | Jan 1, 2009 |
| First posted | Mar 28, 2006 |
| Last update posted | Nov 28, 2012 |
| Countries | United States |
At a glance
- 1–9 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: