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NCT00599716
Phase 3Interventional
Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug.
View on ClinicalTrials.gov ↗Timeline
- Start date
- Dec 1, 2006
- Primary completion
- Apr 1, 2008
- Completion date
- May 1, 2008
- First posted
- —
- Last posted
- —
- Enrollment
- 300
- Arms / groups
- 2 / —
- Source
- AACT · pre-existing
Sponsors
- LantibioLead sponsor
- Chattanooga Eye Institute, Chattanooga, TNOverall official - principal investigator
- Abrams Eye Center, Cleveland, OHOverall official - principal investigator
- Rx Development Resources, LLCStudy chair
- LantibioStudy director
- Rx Development Resources, LLCCollaborator
- LantibioCollaborator
Drugs studied
Indications studied
CDEK-curated fields only — the ClinicalTrials.gov results mirror (baseline measures, adverse events, participant flow) is a separate, currently-dormant pipeline; see MIGRATION_PLAN.md.